共 50 条
- [31] Proximal Microdelection 16p11.2 SyndromeHORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 339 - 340Leo, Francesco论文数: 0 引用数: 0 h-index: 0机构: Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyMadeo, Simona Filomena论文数: 0 引用数: 0 h-index: 0机构: Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyBaraldi, Alessandro论文数: 0 引用数: 0 h-index: 0机构: Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyPredieri, Barbara论文数: 0 引用数: 0 h-index: 0机构: Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyStanghellini, Ilaria论文数: 0 引用数: 0 h-index: 0机构: Clin Genet Unit, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyCalabrese, Olga论文数: 0 引用数: 0 h-index: 0机构: Clin Genet Unit, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, ItalyIughetti, Lorenzo论文数: 0 引用数: 0 h-index: 0机构: Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy Dept Med & Surg Sci Mothers Children & Adults, Modena, Italy
- [32] 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2European Journal of Human Genetics, 2013, 21 : 182 - 189John C K Barber论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineVictoria Hall论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineViv K Maloney论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineShuwen Huang论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineAngharad M Roberts论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineAngela F Brady论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineNicki Foulds论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineBeverley Bewes论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineMarianne Volleth论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineThomas Liehr论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineKarl Mehnert论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineMark Bateman论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic MedicineHelen White论文数: 0 引用数: 0 h-index: 0机构: Faculty of Medicine,Department of Human Genetics and Genomic Medicine
- [33] Chromosomal Deletions at Chromosome 16p11.2 Associated with Severe Early-Onset Obesity-3 Additional PatientsHORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 290 - 290Herrmann, Gloria论文数: 0 引用数: 0 h-index: 0机构: Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, Germany Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, GermanyEhehalt, Stefan论文数: 0 引用数: 0 h-index: 0机构: Publ Hlth Dept Stuttgart, Stuttgart, Germany Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, GermanyBorck, Guntram论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, Ulm, Germany Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, GermanyWabitsch, Martin论文数: 0 引用数: 0 h-index: 0机构: Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, Germany Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, Germanyvon Schnurbein, Julia论文数: 0 引用数: 0 h-index: 0机构: Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, Germany Ctr Rare Endocrine Dis, Div Pediat Endocrinol & Diabet, Dept Pediat & Adolescent Med, Ulm, Germany
- [34] Intrafamilial variability of neuropsychiatric symptoms associated with the microduplication of chromosome 16p11.2EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 268 - 268Arlt, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyKaeseberg, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyLinke, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyWinter, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyBartsch, O.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyDavydenko, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Mainz, Dept Psychiat & Psychotherapy, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanySchweiger, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyTuescher, O.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Mainz, Dept Psychiat & Psychotherapy, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, GermanyKomlosi, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Inst Human Genet, Mainz, Germany Univ Med Ctr, Inst Human Genet, Mainz, Germany
- [35] An examination of frontal asymmetry in relation to eating in the absence of hunger and loss-of-control eatingAPPETITE, 2023, 191Chen, Joanna Y.论文数: 0 引用数: 0 h-index: 0机构: Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA Drexel Univ, Dept Psychol, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USAOh, Yongtaek论文数: 0 引用数: 0 h-index: 0机构: Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA论文数: 引用数: h-index:机构:Lowe, Michael R.论文数: 0 引用数: 0 h-index: 0机构: Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA Drexel Univ, Dept Psychol & Brain Sci, 3141 Chestnut St,Suite 119, Philadelphia, PA 19104 USA
- [36] 16p11.2 microdeletion: The most common chromosomal anomaly associated with obesityEUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2019, 49 : 81 - 82Rosmaninho-salgado, Joana论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalPires, Luis Miguel论文数: 0 引用数: 0 h-index: 0机构: Univ Coimbra, Fac Med, Lab Citogenet & Genom, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalCarreira, Isabel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Coimbra, Fac Med, iCBR CIMAGO Ctr Invest Meio Ambiente Genet & Onco, Coimbra, Portugal Univ Coimbra, Fac Med, Lab Citogenet & Genom, Coimbra, Portugal Univ Coimbra, CNC IBILI, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal论文数: 引用数: h-index:机构:Louro, Pedro论文数: 0 引用数: 0 h-index: 0机构: Inst Portugues Oncol Lisboa, Lisbon, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalSa, Joaquim论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalVenancio, Maria Margarida论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalAlmeida, Pedro论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalRibeiro, Sara论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalSaraiva, Jorge M.论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Univ Coimbra, Fac Med, Clin Univ Pediat, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, PortugalSousa, Sergio B.论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal Univ Coimbra, Fac Med, Inst Genet Med, Coimbra, Portugal Hosp Pediat, Serv Genet Med, CHUC, Coimbra, Portugal
- [37] Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 DuplicationCEREBRAL CORTEX, 2016, 26 (05) : 1957 - 1964Jenkins, Julian, III论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAChow, Vivian论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USABlaskey, Lisa论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAKuschner, Emily论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAQasmieh, Saba论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAGaetz, Leah论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAEdgar, J. Christopher论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAMukherjee, Pratik论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Sch Med, Dept Radiol, San Francisco, CA 94143 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USABuckner, Randall论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Dept Psychol, 33 Kirkland St, Cambridge, MA 02138 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USANagarajan, Srikantan S.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Sch Med, Dept Radiol, San Francisco, CA 94143 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USAChung, Wendy K.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, Med Ctr, New York, NY 10032 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USASpiro, John E.论文数: 0 引用数: 0 h-index: 0机构: Simons Fdn, New York, NY 10010 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USASherr, Elliott H.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA 94143 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USABerman, Jeffrey I.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USARoberts, Timothy P. L.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Radiol, Lurie Family Fdn MEG Imaging Ctr, Philadelphia, PA 19104 USA
- [38] DUPLICATION IN THE 16P11.2 REGION IS ASSOCIATED WITH ALTERED HIPPOCAMPAL MORPHOLOGY IN SCHIZOPHRENIASCHIZOPHRENIA BULLETIN, 2011, 37 : 161 - 162Cronenwett, Will J.论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Chicago, IL 60611 USA Northwestern Univ, Chicago, IL 60611 USADuan, Jubao论文数: 0 引用数: 0 h-index: 0机构: Northshore Univ Hlth Syst, Evanston, IL USA Northwestern Univ, Chicago, IL 60611 USAWang, Lei论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Chicago, IL 60611 USA Northwestern Univ, Chicago, IL 60611 USASanders, Alan R.论文数: 0 引用数: 0 h-index: 0机构: Northshore Univ Hlth Syst, Evanston, IL USA Northwestern Univ, Chicago, IL 60611 USAGejman, Pablo V.论文数: 0 引用数: 0 h-index: 0机构: Northshore Univ Hlth Syst, Evanston, IL USA Northwestern Univ, Chicago, IL 60611 USACsernansky, John G.论文数: 0 引用数: 0 h-index: 0机构: Northwestern Univ, Chicago, IL 60611 USA Northwestern Univ, Chicago, IL 60611 USA
- [39] 16p11.2 microdeletion associated to early onset benign childhood seizuresREVISTA DE NEUROLOGIA, 2013, 56 (02) : 125 - 127Castro-Gago, Manuel论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, Spain Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, SpainPerez-Gay, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, Spain Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, SpainGomez-Lado, Carmen论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, Spain Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, SpainDacruz, David论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, Spain Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, SpainBarros-Angueira, Francisco论文数: 0 引用数: 0 h-index: 0机构: Fdn Publ Gallega Med Xen, Santiago De Compostela, A Coruna, Spain Univ Santiago de Compostela, Hosp Clin Univ, Serv Neuropediat, Santiago De Compostela, A Coruna, Spain
- [40] Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorderJOURNAL OF MEDICAL GENETICS, 2010, 47 (03) : 195 - 203Fernandez, Bridget A.论文数: 0 引用数: 0 h-index: 0机构: Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada Mem Univ Newfoundland, Discipline Genet, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaRoberts, Wendy论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Autism Res Unit, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaChung, Brian论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Pediat, Div Clin & Metab Genet, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaWeksberg, Rosanna论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Pediat, Div Clin & Metab Genet, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaMeyn, Stephen论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Dept Pediat, Div Clin & Metab Genet, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaSzatmari, Peter论文数: 0 引用数: 0 h-index: 0机构: McMaster Univ, Offord Ctr Child Studies, Hamilton, ON, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaJoseph-George, Ann M.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Ctr Appl Gen, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Dept Pediat, Cytogenet Lab, Lab Med, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaMacKay, Sara论文数: 0 引用数: 0 h-index: 0机构: Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaWhitten, Kathy论文数: 0 引用数: 0 h-index: 0机构: Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaNoble, Barbara论文数: 0 引用数: 0 h-index: 0机构: Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaVardy, Cathy论文数: 0 引用数: 0 h-index: 0机构: Mem Univ Newfoundland, Discipline Pediat, St John, NF, Canada Child Hlth Program, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaCrosbie, Victoria论文数: 0 引用数: 0 h-index: 0机构: Child Hlth Program, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaLuscombe, Sandra论文数: 0 引用数: 0 h-index: 0机构: Child Hlth Program, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaTucker, Eva论文数: 0 引用数: 0 h-index: 0机构: Child Hlth Program, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaTurner, Lesley论文数: 0 引用数: 0 h-index: 0机构: Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada Mem Univ Newfoundland, Discipline Genet, St John, NF, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaMarshall, Christian R.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Ctr Appl Gen, Toronto, ON M5G 1X8, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, CanadaScherer, Stephen W.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Ctr Appl Gen, Toronto, ON M5G 1X8, Canada Univ Toronto, Dept Mol Genet, Toronto, ON, Canada Hlth Sci Ctr, Prov Med Genet Program, St John, NF A1B 3V6, Canada