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- [21] Heterozygous loss-of-function ACTB mutations result in a novel developmental syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 99 - 100Cuvertino, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, England论文数: 引用数: h-index:机构:Chandler, K. E.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, EnglandRoberts, N. A.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, EnglandArmstrong, R.论文数: 0 引用数: 0 h-index: 0机构: Addenbrookes Hosp, Cambridge, England Univ Manchester, Manchester, Lancs, EnglandBernardini, L.论文数: 0 引用数: 0 h-index: 0机构: Mendel Lab, Rome, Italy Univ Manchester, Manchester, Lancs, EnglandBhaskar, S.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, England论文数: 引用数: h-index:机构:Clayton-Smith, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, EnglandDavalillo, C. H.论文数: 0 引用数: 0 h-index: 0机构: Quantitat Genom Med Labs, Barcelona, Spain Univ Manchester, Manchester, Lancs, EnglandDeshpande, C.论文数: 0 引用数: 0 h-index: 0机构: Guys Hosp, London, England Univ Manchester, Manchester, Lancs, EnglandDevriendt, K.论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Leuven, Belgium Univ Hosp Leuven, Leuven, Belgium Univ Manchester, Manchester, Lancs, EnglandDigilio, M. C.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Osped Pediat Bambino Gesu, Rome, Italy Univ Manchester, Manchester, Lancs, EnglandDixit, A.论文数: 0 引用数: 0 h-index: 0机构: Nottingham City Hosp, Nottingham, England Univ Manchester, Manchester, Lancs, EnglandEdwards, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Sydney, Sydney, NSW, Australia Univ Manchester, Manchester, Lancs, EnglandFriedman, J. M.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Vancouver, BC, Canada Univ Manchester, Manchester, Lancs, EnglandJoss, S.论文数: 0 引用数: 0 h-index: 0机构: Queen Elizabeth Univ Hosp, Glasgow, Lanark, Scotland Univ Manchester, Manchester, Lancs, EnglandKerr, B.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, EnglandLampe, A. K.论文数: 0 引用数: 0 h-index: 0机构: Western Gen Hosp, Edinburgh, Midlothian, Scotland Univ Manchester, Manchester, Lancs, EnglandMcGowan, R.论文数: 0 引用数: 0 h-index: 0机构: Queen Elizabeth Univ Hosp, Glasgow, Lanark, Scotland Univ Manchester, Manchester, Lancs, EnglandMedt, M. D.论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Leuven, Belgium Univ Hosp Leuven, Leuven, Belgium Univ Manchester, Manchester, Lancs, EnglandO'Sullivan, J.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, EnglandOdent, S.论文数: 0 引用数: 0 h-index: 0机构: Hop SUD, Rennes, France Univ Manchester, Manchester, Lancs, EnglandParker, M. J.论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens NHS Fdn Trust, Sheffield, S Yorkshire, England Univ Manchester, Manchester, Lancs, EnglandPebrel-Richard, C.论文数: 0 引用数: 0 h-index: 0机构: CHU Clermont Ferrand, Clermont Ferrand, France Univ Manchester, Manchester, Lancs, EnglandPetit, F.论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Lille, France Univ Manchester, Manchester, Lancs, EnglandStark, Z.论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Melbourne, Vic, Australia Univ Manchester, Manchester, Lancs, EnglandTinschert, S.论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Innsbruck, Austria Univ Manchester, Manchester, Lancs, EnglandVasudevan, P.论文数: 0 引用数: 0 h-index: 0机构: Leicester Royal Infirm, Leicester, Leics, England Univ Manchester, Manchester, Lancs, EnglandVilla, O.论文数: 0 引用数: 0 h-index: 0机构: Quantitat Genom Med Labs, Barcelona, Spain Univ Manchester, Manchester, Lancs, England论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Woolf, A. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester, Lancs, England Univ Manchester, Manchester, Lancs, England论文数: 引用数: h-index:机构:
- [22] Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphismAMERICAN JOURNAL OF HUMAN GENETICS, 2021, 108 (06) : 1138 - 1150Chopra, Maya论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, France Inst Imagine, F-75015 Paris, France Univ Paris, Lab Embryol & Genet Human Malformat, Inst Imagine, Inst Natl Sante Rech Med INSERM UMR 1163, F-75015 Paris, France Boston Childrens Hosp, Rosamund Stone Zander Translat Neurosci Ctr, Dept Neurol, Boston, MA 02115 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceMcEntagart, Meriel论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ Hosp NHS FT, Dept Med Genet, London SW17 ORE, England Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, France论文数: 引用数: h-index:机构:Platzer, Konrad论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, D-04129 Leipzig, Germany Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceShukla, Anju论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, Karnataka, India Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceGirisha, Katta M.论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, Karnataka, India Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKaur, Anupriya论文数: 0 引用数: 0 h-index: 0机构: PGIMER, Genet Metab Unit, Dept Pediat, Chandigarh 160012, India Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKaur, Parneet论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, Karnataka, India Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FrancePfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, NL-6500 HB Nijmegen, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceVeenstra-Knol, Hermine论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, CB50, Groningen, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceMancini, Grazia M. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Clin Genet, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceCappuccio, Gerarda论文数: 0 引用数: 0 h-index: 0机构: Federico II Univ Naples, Dept Translat Med, Sect Pediat, I-80131 Naples, Italy Telethon Inst Genet & Med, I-80078 Naples, Italy Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceBrunetti-Pierri, Nicola论文数: 0 引用数: 0 h-index: 0机构: Federico II Univ Naples, Dept Translat Med, Sect Pediat, I-80131 Naples, Italy Telethon Inst Genet & Med, I-80078 Naples, Italy Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKortuem, Fanny论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, D-20246 Hamburg, Germany Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHempel, Maja论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, D-20246 Hamburg, Germany Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceDenecke, Jonas论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Inst Human Genet, D-20246 Hamburg, Germany Univ Med Ctr Hamburg Eppendorf, Dept Pediat, D-20246 Hamburg, Germany Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceLehman, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Med Genet, Vancouver, BC V6H 3N1, Canada Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKleefstra, Tjitske论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, NL-6500 HB Nijmegen, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceStuurman, Kyra E.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Clin Genet, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceWilke, Martina论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Clin Genet, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceThompson, Michelle L.论文数: 0 引用数: 0 h-index: 0机构: HudsonAlpha Inst Biotechnol, Huntsville, AL 35806 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceBebin, E. Martina论文数: 0 引用数: 0 h-index: 0机构: Univ Alabama Birmingham, Dept Neurol & Pediat, Birmingham, AL 35294 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceBijlsma, Emilia K.论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Dept Clin Genet, Med Ctr, NL-2300 RC Leiden, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHoffer, Mariette J., V论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Dept Clin Genet, Med Ctr, NL-2300 RC Leiden, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FrancePeeters-Scholte, Cacha论文数: 0 引用数: 0 h-index: 0机构: Leiden Univ, Dept Neurol, Med Ctr, NL-2300 RC Leiden, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceSlavotinek, Anne论文数: 0 引用数: 0 h-index: 0机构: UCSF, Div Genet, Dept Pediat, San Francisco, CA 94158 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceWeiss, William A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94110 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceYip, Tiffany论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHodoglugil, Ugur论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceWhittle, Amy论文数: 0 引用数: 0 h-index: 0机构: UCSF, Dept Pediat, Zuckerberg San Francisco Gen, San Francisco, CA 94143 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceMonda, Janettedi论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceNeira, Juanita论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceYang, Sandra论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Clin Genom Program, 207 Perry Pkwy, Gaithersburg, MD 20877 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKirby, Amelia论文数: 0 引用数: 0 h-index: 0机构: Wake Forest Sch Med, Sect Med Genet, Winston Salem, NC 27157 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FrancePinz, Hailey论文数: 0 引用数: 0 h-index: 0机构: St Louis Univ, Div Med Genet, Sch Med, St Louis, MO 63104 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceLechner, Rosan论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Clin Genet, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceSleutels, Frank论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Rotterdam, Erasmus Med Ctr, Dept Clin Genet, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHelbig, Ingo论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Epilepsy NeuroGenet Initiat ENGIN, Philadelphia, PA 19014 USA Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat DBHi, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Dept Neurol, Philadelphia, PA 19104 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceMcKeown, Sarah论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Epilepsy NeuroGenet Initiat ENGIN, Philadelphia, PA 19014 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHelbig, Katherine论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Epilepsy NeuroGenet Initiat ENGIN, Philadelphia, PA 19014 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceWillaert, Rebecca论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Clin Genom Program, 207 Perry Pkwy, Gaithersburg, MD 20877 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceJuusola, Jane论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Clin Genom Program, 207 Perry Pkwy, Gaithersburg, MD 20877 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceSemotok, Jennifer论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Clin Genom Program, 207 Perry Pkwy, Gaithersburg, MD 20877 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceHadonou, Medard论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ Hosp NHS FT, St Georges Genom Serv, London SW17 ORE, England Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceShort, John论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ Hosp NHS FT, St Georges Genom Serv, London SW17 ORE, England Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceYachelevich, Naomi论文数: 0 引用数: 0 h-index: 0机构: NYU Clin Genet Serv, 145 E 32nd St PH, New York, NY 10016 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceLala, Sajel论文数: 0 引用数: 0 h-index: 0机构: Nickelaus Childrens Hlth Syst, Div Clin Genet, 3100 SW 62nd Ave, Coral Gables, FL 33155 USA Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceFernandez-Jaen, Alberto论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Quironsalud, Dept Pediat Neurol, Madrid 28224, Spain Univ Complutense, Madrid 28224, Spain Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FrancePelayo, Janvier Porta论文数: 0 引用数: 0 h-index: 0机构: Genol Ctr, Malaga 29016, Spain Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, FranceKloeckner, Chiara论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, D-04129 Leipzig, Germany Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, France
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- [24] Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1AMERICAN JOURNAL OF OPHTHALMOLOGY, 2024, 258 : 183 - 195Patterson, Karynne论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAChong, Jessica x.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Brotman Baty Inst Precis Med, Dept Pediat, Seattle, WA 98195 USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAChung, Doug d.论文数: 0 引用数: 0 h-index: 0机构: UCLA, Stein Eye Inst, David Geffen Sch Med, Dept Ophthalmol, Los Angeles, CA 90095 USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USALisch, Walter论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Ophthalmol, D-55131 Mainz, Germany Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAKarp, Carol l.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami Miller, Bascom Palmer Eye Inst, Sch Med, Dept Ophthalmol, Miami, FL USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USADreisler, Erling论文数: 0 引用数: 0 h-index: 0机构: NJespersensvej 3, DK-2000 Copenhagen, Frederiksberg, Denmark Univ Washington, Dept Genome Sci, Seattle, WA 98195 USALockington, David论文数: 0 引用数: 0 h-index: 0机构: Gartnavel Royal Hosp, Tennent Inst Ophthalmol, NHS Greater Glasgow & Clyde, 1053 Great Westem Rd, Glasgow City G12, Scotland Univ Washington, Dept Genome Sci, Seattle, WA 98195 USARohrbach, Jens m.论文数: 0 引用数: 0 h-index: 0机构: Univ Augenklin Tubingen, D-72076 Tubingen, Germany Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAGarczarczyk-asim, Dorota论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAMueller, Thomas论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria Univ Washington, Dept Genome Sci, Seattle, WA 98195 USATuft, Stephen j.论文数: 0 引用数: 0 h-index: 0机构: Moorfields Eye Hosp NHS Fdn Trust, London, England Univ Washington, Dept Genome Sci, Seattle, WA 98195 USASkalicka, Pavlina论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Gen Univ Hosp Prague, Fac Med 1, Dept Ophthalmol, Prague, Czech Republic Charles Univ Prague, Gen Univ Hosp, Fac Med 1, Dept Paediat & Inherited Metab Disorders, Prague, Czech Republic Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAWilnai, Yael论文数: 0 引用数: 0 h-index: 0机构: Genet Inst Inc, Tel Aviv Sourasky Med Ctr, IL-6423906 Tel Aviv, Israel Univ Washington, Dept Genome Sci, Seattle, WA 98195 USASamra, Nadra naser论文数: 0 引用数: 0 h-index: 0机构: Bar Ilan Univ Fac Med, Sieff Hosp, Genet Unit, Safed, Israel Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAIbrahim, Ali论文数: 0 引用数: 0 h-index: 0机构: Magdal Shams Med Ctr, Maccabi & Clalit Hlth Serv, Ophthalmol unit, Golan Hts, Israel Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAMandel, Hanna论文数: 0 引用数: 0 h-index: 0机构: Bar Ilan Univ, Sieff Hosp, Fac Med, Pediat Metab Clin, Ramat Gan, Israel Univ Washington, Dept Genome Sci, Seattle, WA 98195 USADavidson, Alice e.论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, England Univ Washington, Dept Genome Sci, Seattle, WA 98195 USALiskova, Petra论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Gen Univ Hosp Prague, Fac Med 1, Dept Ophthalmol, Prague, Czech Republic Charles Univ Prague, Gen Univ Hosp, Fac Med 1, Dept Paediat & Inherited Metab Disorders, Prague, Czech Republic Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAAldave, Anthony j.论文数: 0 引用数: 0 h-index: 0机构: UCLA, Stein Eye Inst, David Geffen Sch Med, Dept Ophthalmol, Los Angeles, CA 90095 USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USABamshad, Michael j.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA Univ Washington, Dept Genome Sci, Seattle, WA 98195 USAJanecke, Andreas r.论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria Med Univ Innsbruck, Div Human Genet, A-6020 Innsbruck, Austria Med Univ Innsbruck, Dept Pediatr 1, Div Human Genet, Innsbruck, Austria Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
- [25] Loss of Function Variants in the CSTB Gene Cause Microcephaly, Developmental Delay, Hyperkinetic Movements, and Early Onset EpilepsyNEUROLOGY, 2019, 92 (15)Rogers, Amanda论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Pediat Neurol, St Louis, MO 63110 USA Washington Univ, Pediat Neurol, St Louis, MO 63110 USAShinawi, Marwan论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Pediat Neurol, St Louis, MO 63110 USAPearson, Toni论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Pediat Neurol, St Louis, MO USA Washington Univ, Pediat Neurol, St Louis, MO 63110 USA
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BrazilMoshiri, Ala论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Sch Med, Dept Ophthalmol & Vis Sci, Sacramento, CA 95817 USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilWillis, Brandon论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Mouse Biol Program, Davis, CA 95616 USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilLanoue, Louise论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Mouse Biol Program, Davis, CA 95616 USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilBower, Lynette论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Mouse Biol Program, Davis, CA 95616 USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilLeonard, Brian C.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Davis, Sch Vet Med, Dept Surg & Radiol Sci, Davis, CA 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Paulo论文数: 0 引用数: 0 h-index: 0机构: Mendelics, Sao Paulo, SP, Brazil Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilMonteiro, Fabiola P.论文数: 0 引用数: 0 h-index: 0机构: Mendelics, Sao Paulo, SP, Brazil Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilZatz, Mayana论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, Brazil Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilMenck, Carlos Frederico Martins论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Inst Biomed Sci, Dept Microbiol, Sao Paulo, SP, Brazil Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilWheeler, Matthew T.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Div Cardiovasc Med, Dept Med, Sch Med, Stanford, CA USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilBernstein, Jonathan A.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Div Med Genet, Dept Pediat, Sch Med, Stanford, CA USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilDumas, Kevin论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Pathol, Clin Genom Program, Stanford, CA USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilSpiteri, Elizabeth论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Pathol, Clin Genom Program, Stanford, CA USA Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, Brazil论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Hashem, Mais论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh, Saudi Arabia Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilAlsaif, Hessa S.论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh, Saudi Arabia Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilChedrawi, Aziza论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Neurosci, Riyadh, Saudi Arabia Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilAlkuraya, Fowzan S.论文数: 0 引用数: 0 h-index: 0机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh, Saudi Arabia Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, SP, BrazilKok, Fernando论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Biosci Inst, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, Sao Paulo, 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- [29] Both Heterozygous and Homozygous Loss-of-Function JPH3 Variants Are Associated with a Paroxysmal Movement DisorderMOVEMENT DISORDERS, 2023, 38 (01) : 155 - 157Steel, Dora论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England Great Ormond St Hosp Sick Children, Dept Neurol, London, England UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, EnglandVezyroglou, Aikaterini论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England Great Ormond St Hosp Sick Children, Dept Neurol, London, England UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, EnglandBarwick, Katy论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England论文数: 引用数: h-index:机构:Vogt, Julie论文数: 0 引用数: 0 h-index: 0机构: Birmingham Women & Childrens Hosp NHS Fdn Trust, West Midlands Reg Genet Serv, Birmingham, W Midlands, England UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, EnglandGibbon, Frances M.论文数: 0 引用数: 0 h-index: 0机构: Cardiff & Vale Univ Hlth Board, Noahs Ark Childrens Hosp Wales, Cardiff, Wales UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, EnglandCross, J. Helen论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England Great Ormond St Hosp Sick Children, Dept Neurol, London, England UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, EnglandKurian, Manju A.论文数: 0 引用数: 0 h-index: 0机构: UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England Great Ormond St Hosp Sick Children, Dept Neurol, London, England UCL Great Ormond St Inst Child Hlth, Zayed Ctr Res Rare Dis Children, Dev Neurosci, London, England
- [30] Developmental delay and failure to thrive associated with a loss-of-function variant in WHSC1 (NSD2)AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (12) : 2798 - 2802Boczek, Nicole J.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USALahner, Carrie A.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USAThuy-mi Nguyen论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Clin Genom, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USAFerber, Matthew J.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Clin Genom, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USAHasadsri, Linda论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USAThorland, Erik C.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Clin Genom, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USANiu, Zhiyv论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA Mayo Clin, Dept Clin Genom, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USAGavrilova, Ralitza H.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Clin Genom, Rochester, MN USA Mayo Clin, Dept Neurol, Rochester, MN USA Mayo Clin, Dept Lab Med & Pathol, Genom Lab, Rochester, MN USA