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- [41] Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two CasesFRONTIERS IN GENETICS, 2021, 12Zarate, Yuri A.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAVernon, Hilary J.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Genet, Baltimore, MD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USABosanko, Katherine A.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USARamani, Praveen K.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Dept Pediat Neurol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAGokden, Murat论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Dept Pathol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAWritzl, Karin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Ljubljana, Clin Inst Med Genet, Ljubljana, Slovenia Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAMeznaric, Marija论文数: 0 引用数: 0 h-index: 0机构: Univ Ljubljana, Inst Anat, Fac Med, Ljubljana, Slovenia Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAVipotnik Vesnaver, Tina论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Ljubljana, Dept Radiol, Ljubljana, Slovenia Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USARamakrishnaiah, Raghu论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Div Neuroradiol & Pediat Radiol, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAOsredkar, Damjan论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Ljubljana, Univ Childrens Hosp, Dept Pediat Neurol, Ljubljana, Slovenia Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA
- [42] Cytogenetically pseudobalanced chromosome 2 structural rearrangements associated with 2q23.1 microdeletion syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 983 - 983Kolotii, A. D.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaVorsanova, S. G.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaYurov, Y. B.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaKurinnaia, O. S.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaZelenova, M. A.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaBulatnikova, M. A.论文数: 0 引用数: 0 h-index: 0机构: Stem Cell Bank Pokrovsky, St Petersburg, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, RussiaIourov, I. Y.论文数: 0 引用数: 0 h-index: 0机构: NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia FSBSI Mental Hlth Res Ctr, Moscow, Russia FSBEI FPE Russian Med Acad Postgrad Educ, Minist Healthcare Russian Federat, Moscow, Russia NI Pirogov Russian Natl Res Med Univ, Acad YuE Veltishchev Res Clin Inst Pediat, Minist Hlth Russian Federat, Moscow, Russia
- [43] Vascular Ehlers Danlos syndrome as part of 2q32.2q33.1 microdeletion syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 227 - 227Green, C.论文数: 0 引用数: 0 h-index: 0机构: Sheffield Clin Genet, Sheffield, S Yorkshire, England Sheffield Clin Genet, Sheffield, S Yorkshire, EnglandHobson, E.论文数: 0 引用数: 0 h-index: 0机构: Yorkshire Reg Genet Serv, Leeds, W Yorkshire, England Sheffield Clin Genet, Sheffield, S Yorkshire, EnglandRadley, J.论文数: 0 引用数: 0 h-index: 0机构: West Midlands Clin Genet Serv, Birmingham, W Midlands, England Sheffield Clin Genet, Sheffield, S Yorkshire, EnglandWilliams, D.论文数: 0 引用数: 0 h-index: 0机构: West Midlands Clin Genet Serv, Birmingham, W Midlands, England Sheffield Clin Genet, Sheffield, S Yorkshire, EnglandJohnson, D.论文数: 0 引用数: 0 h-index: 0机构: Sheffield Clin Genet, Sheffield, S Yorkshire, England Sheffield Clin Genet, Sheffield, S Yorkshire, England
- [44] CHILDREN WITH SATB2-ASSOCIATED SYNDROME HAVE INCREASED EMOTIONAL, BEHAVIOR, AND SLEEP DISTURBANCESJOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2020, 59 (10): : S188 - S188Leo, Elaine论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas, Fayetteville, AR 72701 USA Univ Arkansas, Fayetteville, AR 72701 USA论文数: 引用数: h-index:机构:Gokarakonda, Srinivasa B.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas, Fayetteville, AR 72701 USA Univ Arkansas, Fayetteville, AR 72701 USACaffrey, Aisling R.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas, Fayetteville, AR 72701 USA Univ Arkansas, Fayetteville, AR 72701 USAZarate, Yuri A.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas, Fayetteville, AR 72701 USA Univ Arkansas, Fayetteville, AR 72701 USA
- [45] Neurological manifestations of 2q31 microdeletion syndromeCONGENITAL ANOMALIES, 2017, 57 (06) : 197 - 200Okamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Med Genet, 840 Murodo Cho, Izumi, Osaka 5941101, Japan Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Med Genet, 840 Murodo Cho, Izumi, Osaka 5941101, JapanKimura, Sadami论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Pediat Neurol, Osaka, Japan Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Med Genet, 840 Murodo Cho, Izumi, Osaka 5941101, JapanShimojima, Keiko论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Inst Med Genet, Tokyo, Japan Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Med Genet, 840 Murodo Cho, Izumi, Osaka 5941101, JapanYamamoto, Toshiyuki论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Inst Med Genet, Tokyo, Japan Osaka Med Ctr & Res Inst Maternal & Child Hlth, Dept Med Genet, 840 Murodo Cho, Izumi, Osaka 5941101, Japan
- [46] Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndromeGENES BRAIN AND BEHAVIOR, 2021, 20 (07)Snijders Blok, Lot论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlands Max Planck Inst Psycholinguist, Language & Genet Dept, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, NetherlandsGoosen, Y. Max论文数: 0 引用数: 0 h-index: 0机构: Vincent Van Gogh Inst Psychiat, Ctr Excellence Neuropsychiat, Venray, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlandsvan Haaften, Leenke论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Rehabil, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlandsvan Hulst, Karen论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Rehabil, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, NetherlandsFisher, Simon E.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Psycholinguist, Language & Genet Dept, Nijmegen, Netherlands Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Ctr Neurosci, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, NetherlandsBrunner, Han G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Maastricht Univ, Med Ctr, MHeNS Sch Neurosci, Dept Clin Genet, Maastricht, Netherlands Maastricht Univ, Med Ctr, GROW Sch Oncol & Dev Biol, Maastricht, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, NetherlandsEgger, Jos I. M.论文数: 0 引用数: 0 h-index: 0机构: Vincent Van Gogh Inst Psychiat, Ctr Excellence Neuropsychiat, Venray, Netherlands Dichterbij, Stevig Specialized & Forens Care People Intellect, Oostrum, Netherlands Radboud Univ Nijmegen, Ctr Cognit, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, NetherlandsKleefstra, Tjitske论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands Vincent Van Gogh Inst Psychiat, Ctr Excellence Neuropsychiat, Venray, Netherlands Radboud Univ Nijmegen, Med Ctr, Human Genet, Nijmegen, Netherlands
- [47] Further Supporting Evidence for the SATB2-Associated Syndrome Found Through Whole Exome SequencingAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (05) : 1026 - 1032Zarate, Yuri A.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAPerry, Hazel论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Orofacial Sci, Div Craniofacial Anomalies, San Francisco, CA 94143 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USABen-Omran, Tawfeg论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Dept Pediat, Clin & Metab Genet, Doha, Qatar Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USASellars, Elizabeth A.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAStein, Quinn论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hosp, Div Pediat Neurol, Sanford Childrens Specialty Clin, Sioux Falls, SD USA Sanford Childrens Hosp, Div Genet, Sanford Childrens Specialty Clin, Sioux Falls, SD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAAlmureikhi, Mariam论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Dept Pediat, Clin & Metab Genet, Doha, Qatar Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USASimmons, Kirk论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Dept Dent, Little Rock, AR 72205 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAKlein, Ophir论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Orofacial Sci, Div Craniofacial Anomalies, San Francisco, CA 94143 USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAFish, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Orthopaed Surg, San Francisco, CA USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAFeingold, Murray论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Feingold Ctr, Div Genet & Genom, Boston, MA USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USADouglas, Jessica论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Feingold Ctr, Div Genet & Genom, Boston, MA USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAKruer, Michael C.论文数: 0 引用数: 0 h-index: 0机构: Sanford Childrens Hosp, Div Pediat Neurol, Sanford Childrens Specialty Clin, Sioux Falls, SD USA Sanford Childrens Hosp, Div Genet, Sanford Childrens Specialty Clin, Sioux Falls, SD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USASi, Yue论文数: 0 引用数: 0 h-index: 0机构: ARUP Labs, Mol Genet & Genom, Salt Lake City, UT USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAMao, Rong论文数: 0 引用数: 0 h-index: 0机构: ARUP Labs, Mol Genet & Genom, Salt Lake City, UT USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAMcKnight, Dianalee论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USAGibellini, Federica论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USARetterer, Kyle论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USASlavotinek, Anne论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Dept Pediat, Div Genet, San Francisco, CA USA Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA
- [48] The behavioural phenotype of SATB2-associated syndrome: a within-group and cross-syndrome analysisJOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2022, 14 (01)论文数: 引用数: h-index:机构:Oliver, Chris论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandMoss, Joanna论文数: 0 引用数: 0 h-index: 0机构: Univ Surrey, Sch Psychol, Guildford, Surrey, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandHeald, Mary论文数: 0 引用数: 0 h-index: 0机构: Blackpool Teaching Hosp NHS Fdn Trust, Blackpool, Lancs, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandWaite, Jane论文数: 0 引用数: 0 h-index: 0机构: Aston Univ, Sch Hlth & Life Sci, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandCrawford, Hayley论文数: 0 引用数: 0 h-index: 0机构: Univ Warwick, Warwick Med Sch, Mental Hlth & Wellbeing Unit, Coventry, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandKothari, Vishakha论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandRumbellow, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandWalters, Grace论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, EnglandRichards, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England Univ Birmingham, Sch Psychol, Birmingham, W Midlands, England
- [49] An atypical autistic phenotype associated with a 2q13 microdeletion: A case reportJournal of Medical Case Reports, 12 (1)Guivarch J.论文数: 0 引用数: 0 h-index: 0机构: Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, MarseilleChatel C.论文数: 0 引用数: 0 h-index: 0机构: PACA Autism Resource Center, APHM, Sainte Marguerite Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, MarseilleMortreux J.论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics, Cytogenetics Laboratory, APHM, Timone Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, MarseilleMissirian C.论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics, Cytogenetics Laboratory, APHM, Timone Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, MarseillePhilip N.论文数: 0 引用数: 0 h-index: 0机构: Department of Medical Genetics, Referral Center for Developmental Anomalies, Aix-Marseille University, APHM, GMGF, Timone Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, MarseillePoinso F.论文数: 0 引用数: 0 h-index: 0机构: Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, Marseille Department of Child Psychiatry, Aix-Marseille University, APHM, Sainte Marguerite Hospital, Marseille
- [50] Craniofacial and dental characteristics of three Japanese individuals with genetically diagnosed SATB2-associated syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (07) : 1984 - 1989Kurosaka, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, 1-8 Yamadaoka, Suita, Osaka 5650871, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanYamamoto, Sayuri论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanHirasawa, Kyoko论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Dept Pediat, Tokyo, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanYanagishita, Tomoe论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Inst Med Genet, Tokyo, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanFujioka, Kaoru论文数: 0 引用数: 0 h-index: 0机构: Univ Yamanashi, Fac Med, Dept Pediat, Yamanashi, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanYagasaki, Hideaki论文数: 0 引用数: 0 h-index: 0机构: Univ Yamanashi, Fac Med, Dept Pediat, Yamanashi, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanNagata, Miho论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Cardiovasc Med, Grad Sch Med, Osaka, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan论文数: 引用数: h-index:机构:Yonei, Ayumi论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ Hosp, Dept Genet Counseling, Osaka, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan论文数: 引用数: h-index:机构:Nagata, Namiki论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanTsujimoto, Takayuki论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanInubushi, Toshihiro论文数: 0 引用数: 0 h-index: 0机构: Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, JapanYamamoto, Toshiyuki论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Inst Med Genet, Tokyo, Japan Osaka Univ, Dept Orthodont & Dentofacial Orthoped, Grad Sch Dent, Suita, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构: