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Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders.
McGee, Stacey R; Rajamanickam, Shivakumar; Adhikari, Sandeep; Falayi, Oluwatosin C; Wilson, Theresa A; Shayota, Brian J; Cooley Coleman, Jessica A; Skinner, Cindy; Caylor, Raymond C; Stevenson, Roger E; Quaio, Caio Robledo D' Angioli Costa; Wilke, Berenice Cunha; Bain, Jennifer M; Anyane-Yeboa, Kwame; Brown, Kaitlyn; Greally, John M; Bijlsma, Emilia K; Ruivenkamp, Claudia A L; Politi, Keren; Arbogast, Lydia A; Collard, Michael W; Huggenvik, Jodi I; Elsea, Sarah H; Jensik, Philip J.
Affiliation
  • McGee SR; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL USA.
  • Rajamanickam S; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL USA.
  • Adhikari S; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL USA.
  • Wilson TA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, USA.
  • Shayota BJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, USA.
  • Cooley Coleman JA; Department of Pediatrics, Division of Genetics, University of Utah, Salt Lake City, UT.
  • Skinner C; Greenwood Genetic Center, Greenwood, SC, USA.
  • Caylor RC; Greenwood Genetic Center, Greenwood, SC, USA.
  • Stevenson RE; Greenwood Genetic Center, Greenwood, SC, USA.
  • Quaio CRAC; Greenwood Genetic Center, Greenwood, SC, USA.
  • Wilke BC; Instituto da Criança (Children's Hospital), Hospital das Clínicas (HCFMUSP), Faculdade de Medicina (FMUSP), Universidade de São Paulo, São Paulo, SP, Brazil.
  • Bain JM; Laboratório Clínico, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
  • Anyane-Yeboa K; Unicamp, Campinas, SP, Brazil.
  • Brown K; Department of Neurology, Division of Child Neurology, Columbia University Irving Medical Center, New York, USA.
  • Greally JM; Department of Pediatrics, Division of Clinical Genetics, Columbia University Irving Medical Center, New York, USA.
  • Bijlsma EK; Departments of Pediatrics and Genetics, Albert Einstein College of Medicine, Bronx, NY USA.
  • Ruivenkamp CAL; Departments of Pediatrics and Genetics, Albert Einstein College of Medicine, Bronx, NY USA.
  • Politi K; Departments of Genetics, Albert Einstein College of Medicine, Bronx, NY USA.
  • Arbogast LA; Department of Clinical Genetics, Leiden University Medical Centre, PO box 9600, 2300 RC, Leiden, The Netherlands.
  • Collard MW; Department of Clinical Genetics, Leiden University Medical Centre, PO box 9600, 2300 RC, Leiden, The Netherlands.
  • Huggenvik JI; ALYN Hospital, Jerusalem, Israel.
  • Elsea SH; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL USA.
  • Jensik PJ; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL USA.
Hum Mol Genet ; 32(3): 386-401, 2023 01 13.
Article in En | MEDLINE | ID: mdl-35981081
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurodevelopmental Disorders / Autism Spectrum Disorder Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2023 Document type: Article Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neurodevelopmental Disorders / Autism Spectrum Disorder Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2023 Document type: Article Country of publication: