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- [1] A Fetus with 17q23.1-q23.2 Microdeletion Presents with Primary Bilateral Lung Hypoplasia in UteroFETAL AND PEDIATRIC PATHOLOGY, 2023, 42 (01) : 144 - 148Yao, Longmei论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R China Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R ChinaXu, Yan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R China Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R ChinaDeng, Yan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R China Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R ChinaZeng, Shi论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R China Cent South Univ, Xiangya Hosp 2, Dept Ultrasound Diag, Changsha, Peoples R China
- [2] Familial Microduplication of 17q23.1-q23.2 Involving TBX4 is Associated With Congenital Clubfoot and Reduced Penetrance in FemalesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (02) : 364 - 369Peterson, Jess F.论文数: 0 引用数: 0 h-index: 0机构: UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USA Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USAGhaloul-Gonzalez, Lina论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp Pittsburgh, Dept Med Genet, Pittsburgh, PA 15213 USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USAMadan-Khetarpal, Suneeta论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp Pittsburgh, Dept Med Genet, Pittsburgh, PA 15213 USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USAHartman, Jessica论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp Pittsburgh, Dept Med Genet, Pittsburgh, PA 15213 USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USASurti, Urvashi论文数: 0 引用数: 0 h-index: 0机构: UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USA Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USARajkovic, Aleksandar论文数: 0 引用数: 0 h-index: 0机构: UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USA Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USAYatsenko, Svetlana A.论文数: 0 引用数: 0 h-index: 0机构: UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USA Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA UPMC, Magee Womens Hosp, Ctr Med Genet & Genom, Pittsburgh Cytogenet Lab, Pittsburgh, PA 15213 USA
- [3] A Rare Case Report of 17q23.1q23.2 Microdeletion With Homozygosity of 11p11.2q13.4 in a NewbornCUREUS JOURNAL OF MEDICAL SCIENCE, 2022, 14 (03)Barola, Sindhu论文数: 0 引用数: 0 h-index: 0机构: Nassau Univ, Pediat, Med Ctr, E Meadow, NY USA Nassau Univ, Pediat, Med Ctr, E Meadow, NY USAParrill, Allison M.论文数: 0 引用数: 0 h-index: 0机构: Amer Univ, Caribbean Sch Med, Clin Med, Cupecoy, Sint Maarten Nassau Univ, Pediat, Med Ctr, E Meadow, NY USAMahmoudzadeh, Samaan论文数: 0 引用数: 0 h-index: 0机构: Amer Univ, Caribbean Sch Med, Basic Sci, Cupecoy, Sint Maarten Nassau Univ, Pediat, Med Ctr, E Meadow, NY USABizargity, Peyman论文数: 0 引用数: 0 h-index: 0机构: Northwell Hlth, Med Genet, Great Neck, NY USA Nassau Univ, Pediat, Med Ctr, E Meadow, NY USAVerma, Rita论文数: 0 引用数: 0 h-index: 0机构: Nassau Univ, Neonatol, Med Ctr, E Meadow, NY USA Nassau Univ, Pediat, Med Ctr, E Meadow, NY USA
- [4] Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb AbnormalitiesAMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (03) : 454 - 461Ballif, Blake C.论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USATheisen, Aaron论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USARosenfeld, Jill A.论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USATraylor, Ryan N.论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USA论文数: 引用数: h-index:机构:Thrush, Devon Lamb论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Dept Lab Med, Columbus, OH 43209 USA Ohio State Univ, Dept Pediat, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USAAstbury, Caroline论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Dept Lab Med, Columbus, OH 43209 USA Ohio State Univ, Dept Pediat, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USABartholomew, Dennis论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Dept Pediat, Columbus, OH 43209 USA Nationwide Childrens Hosp, Genet Sect, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USAMcBride, Kim L.论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Dept Pediat, Columbus, OH 43209 USA Nationwide Childrens Hosp, Res Inst, Ctr Mol & Human Genet, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USAPyatt, Robert E.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Dept Lab Med, Columbus, OH 43209 USA Ohio State Univ, Dept Pathol, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USAShane, Kate论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Dept Pediat, Columbus, OH 43209 USA Nationwide Childrens Hosp, Genet Sect, Columbus, OH 43209 USA Signature Genom Labs, Spokane, WA 99207 USASmith, Wendy E.论文数: 0 引用数: 0 h-index: 0机构: Maine Pediat Specialty Grp, Dept Pediat, Portland, ME 04102 USA Signature Genom Labs, Spokane, WA 99207 USABanks, Valerie论文数: 0 引用数: 0 h-index: 0机构: Maine Pediat Specialty Grp, Dept Pediat, Portland, ME 04102 USA Signature Genom Labs, Spokane, WA 99207 USAGallentine, William B.论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA Signature Genom Labs, Spokane, WA 99207 USABrock, Pamela论文数: 0 引用数: 0 h-index: 0机构: Univ Louisville, Weisskopf Child Evaluat Ctr, Louisville, KY 40202 USA Signature Genom Labs, Spokane, WA 99207 USARudd, M. Katharine论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA Signature Genom Labs, Spokane, WA 99207 USAAdam, Margaret P.论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA Signature Genom Labs, Spokane, WA 99207 USAKeene, Julia A.论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA Signature Genom Labs, Spokane, WA 99207 USAPhillips, John A., III论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA Signature Genom Labs, Spokane, WA 99207 USAPfotenhauer, Jean P.论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Med Ctr, Div Genet & Genom Med, Nashville, TN 37232 USA Signature Genom Labs, Spokane, WA 99207 USAGowans, Gordon C.论文数: 0 引用数: 0 h-index: 0机构: Univ Louisville, Weisskopf Child Evaluat Ctr, Louisville, KY 40202 USA Signature Genom Labs, Spokane, WA 99207 USAStankiewicz, Pawel论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Human & Mol Genet, Houston, TX 77030 USA Inst Mother & Child Hlth, Dept Med Genet, PL-01211 Warsaw, Poland Signature Genom Labs, Spokane, WA 99207 USABejjani, Bassem A.论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USAShaffer, Lisa G.论文数: 0 引用数: 0 h-index: 0机构: Signature Genom Labs, Spokane, WA 99207 USA Signature Genom Labs, Spokane, WA 99207 USA
- [5] 17q12 Microdeletion Syndrome: Three Patients Illustrating the Phenotypic SpectrumAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (09) : 2317 - 2321Dixit, Abhijit论文数: 0 引用数: 0 h-index: 0机构: City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandPatel, Chirag论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandHarrison, Rachel论文数: 0 引用数: 0 h-index: 0机构: City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandJarvis, Joanna论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, W Midlands Reg Genet Serv, Birmingham, W Midlands, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandHulton, Sally论文数: 0 引用数: 0 h-index: 0机构: Birmingham Childrens Hosp, Dept Paediat Nephrol, Birmingham, W Midlands, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandSmith, Nigel论文数: 0 引用数: 0 h-index: 0机构: City Hosp Nottingham, Dept Cytogenet, Nottingham NG5 1PB, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandYates, Katherine论文数: 0 引用数: 0 h-index: 0机构: City Hosp Nottingham, Dept Cytogenet, Nottingham NG5 1PB, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandSilcock, Lee论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, Dept Mol Cytogenet, Birmingham, W Midlands, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandMcMullan, Dominic J.论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, Dept Mol Cytogenet, Birmingham, W Midlands, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, EnglandSuri, Mohnish论文数: 0 引用数: 0 h-index: 0机构: City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, England City Hosp Nottingham, Dept Clin Genet, Nottingham NG5 1PB, England
- [6] 产前诊断原发性肺发育不良并17q23.1-q23.2微缺失1例中国医学影像学杂志, 2021, 29 (03) : 269 - 270邓妍论文数: 0 引用数: 0 h-index: 0机构: 中南大学湘雅二医院超声诊断科曾施论文数: 0 引用数: 0 h-index: 0机构: 中南大学湘雅二医院超声诊断科徐燕论文数: 0 引用数: 0 h-index: 0机构: 中南大学湘雅二医院超声诊断科
- [7] A case with 10q22.3q23.2 microdeletion syndrome and mosaic Klinefelter syndromeJOURNAL OF BIOTECHNOLOGY, 2018, 280 : S64 - S64Bir, Firdevs Dincsoy论文数: 0 引用数: 0 h-index: 0机构: Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, TurkeyOzdemir, Ozturk论文数: 0 引用数: 0 h-index: 0机构: Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, TurkeyKarakaya, Taner论文数: 0 引用数: 0 h-index: 0机构: Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, TurkeyYildiz, Onur论文数: 0 引用数: 0 h-index: 0机构: Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, TurkeySilan, Fatma论文数: 0 引用数: 0 h-index: 0机构: Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey Canakkale Onsekiz Mart Univ, Med Fac, Dept Med Genet, Canakkale, Turkey
- [8] Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromeJOURNAL OF MEDICAL GENETICS, 2009, 46 (07) : 480 - 489Tan, T. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaAftimos, S.论文数: 0 引用数: 0 h-index: 0机构: Auckland Hosp, No Reg Genet Serv, Auckland, New Zealand Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaWorgan, L.论文数: 0 引用数: 0 h-index: 0机构: Liverpool Hosp, Dept Clin Genet, Liverpool, Merseyside, England Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaSusman, R.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia Childrens Hosp Westmead, Dept Cytogenet, Western Sydney Genet Program, Sydney, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaWilson, M.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia Childrens Hosp Westmead, Dept Cytogenet, Western Sydney Genet Program, Sydney, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaGhedia, S.论文数: 0 引用数: 0 h-index: 0机构: Sydney Childrens Hosp, Dept Med Genet, Randwick, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaKirk, E. P.论文数: 0 引用数: 0 h-index: 0机构: Sydney Childrens Hosp, Dept Med Genet, Randwick, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaLove, D.论文数: 0 引用数: 0 h-index: 0机构: Auckland Hosp, LabPLUS, Auckland, New Zealand Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaRonan, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Newcastle, Callaghan, NSW 2308, Australia Hunter Genet Unit, Waratah, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaDarmanian, A.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia Childrens Hosp Westmead, Dept Cytogenet, Western Sydney Genet Program, Sydney, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaSlavotinek, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaHogue, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA 94143 USA Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaMoeschler, J. B.论文数: 0 引用数: 0 h-index: 0机构: Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaOzmore, J.论文数: 0 引用数: 0 h-index: 0机构: Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaWidmer, R.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Dent, Sydney, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaSavarirayan, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, AustraliaPeters, G.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW, Australia Childrens Hosp Westmead, Dept Cytogenet, Western Sydney Genet Program, Sydney, NSW, Australia Univ Melbourne, Genet Hlth Serv Victoria, Royal Childrens Hosp, Murdoch Childrens Res Inst,Dept Paediat, Melbourne, Vic, Australia
- [9] The 2q23.1 microdeletion syndrome: clinical and behavioural phenotypeEuropean Journal of Human Genetics, 2010, 18 : 163 - 170Bregje WM van Bon论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDavid A Koolen论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLouise Brueton论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDominic McMullan论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsKlaske D Lichtenbelt论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLesley C Adès论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsGregory Peters论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsKate Gibson论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsFrancesca Novara论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsTiziano Pramparo论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsBernardo Dalla Bernardina论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsLeonardo Zoccante论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsUmberto Balottin论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsFausta Piazza论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsVanna Pecile论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsPaolo Gasparini论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsVeronica Guerci论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMarleen Kets论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsRolph Pfundt论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsArjan P de Brouwer论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsJoris A Veltman论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsNicole de Leeuw论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMeredith Wilson论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsJayne Antony论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsSantina Reitano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsDaniela Luciano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsMarco Fichera论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsCorrado Romano论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsHan G Brunner论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsOrsetta Zuffardi论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human GeneticsBert BA de Vries论文数: 0 引用数: 0 h-index: 0机构: Radboud University Nijmegen Medical Centre,Department of Human Genetics
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