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Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Steele, Jacqueline L; Morrow, Michelle M; Sarnat, Harvey B; Alkhunaizi, Ebba; Brandt, Tracy; Chitayat, David A; DeFilippo, Colette P; Douglas, Ganka V; Dubbs, Holly A; Elloumi, Houda Zghal; Glassford, Megan R; Hannibal, Mark C; Héron, Bénédicte; Kim, Linda E; Marco, Elysa J; Mignot, Cyril; Monaghan, Kristin G; Myers, Kenneth A; Parikh, Sumit; Quinonez, Shane C; Rajabi, Farrah; Shankar, Suma P; Shinawi, Marwan S; van de Kamp, Jiddeke J P; Veerapandiyan, Aravindhan; Waldman, Amy T; Graf, William D.
Afiliación
  • Steele JL; University of Connecticut School of Medicine, Farmington, Connecticut.
  • Morrow MM; GeneDx, Inc., Gaithersburg, Maryland.
  • Sarnat HB; Departments of Paediatrics, Pathology (Neuropathology), and Clinical Neurosciences, University of Calgary Cumming School of Medicine and Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
  • Alkhunaizi E; Department of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Brandt T; GeneDx, Inc., Gaithersburg, Maryland.
  • Chitayat DA; Department of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
  • DeFilippo CP; Division of Genomic Medicine, Department of Pediatrics, MIND Institute, University of California-Davis, Sacramento, California.
  • Douglas GV; GeneDx, Inc., Gaithersburg, Maryland.
  • Dubbs HA; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Elloumi HZ; GeneDx, Inc., Gaithersburg, Maryland.
  • Glassford MR; Division of Pediatric Genetics, Metabolism and Genomic Medicine, Department of Pediatrics, C. S. Mott Children's Hospital, University of Michigan, Ann Arbor, Michigan.
  • Hannibal MC; Division of Pediatric Genetics, Metabolism and Genomic Medicine, Department of Pediatrics, C. S. Mott Children's Hospital, University of Michigan, Ann Arbor, Michigan.
  • Héron B; Hôpital Armand Trousseau, Service de Neurologie Pédiatrique, Paris, France.
  • Kim LE; Department of Laboratory Medicine and Genetics, Trillium Health Partners, Mississauga, Ontario, Canada.
  • Marco EJ; Department of Neurodevelopmental Medicine, CorticaCare, San Diego, California.
  • Mignot C; Clinical Genetic Department, Pitié Salpétrière University Hospital, Paris, France.
  • Monaghan KG; GeneDx, Inc., Gaithersburg, Maryland.
  • Myers KA; Division of Neurology, Department of Pediatrics, McGill University Health Centre, Montreal, Canada.
  • Parikh S; Department of Mitochondrial Medicine & Genetics, Cleveland Clinic, Cleveland, Ohio.
  • Quinonez SC; Division of Pediatric Genetics, Metabolism and Genomic Medicine, Department of Pediatrics, C. S. Mott Children's Hospital, University of Michigan, Ann Arbor, Michigan.
  • Rajabi F; Division of Genetics and Genomics, Boston Children's Hospital; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Shankar SP; Division of Genomic Medicine, Department of Pediatrics, MIND Institute, University of California-Davis, Sacramento, California.
  • Shinawi MS; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri.
  • van de Kamp JJP; Clinical Genetics, Amsterdam University Medical Centers, Amsterdam Netherlands.
  • Veerapandiyan A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, Little Rock, Arkansas.
  • Waldman AT; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Graf WD; Division of Neurology, Department of Pediatrics, Connecticut Children's, University of Connecticut, Farmington, Connecticut. Electronic address: wgraf@connecticutchildrens.org.
Pediatr Neurol ; 126: 65-73, 2022 01.
Article en En | MEDLINE | ID: mdl-34740135
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Receptores de Superficie Celular / Semaforinas / Trastorno del Espectro Autista / Discapacidad Intelectual / Proteínas del Tejido Nervioso Tipo de estudio: Guideline / Prognostic_studies Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Receptores de Superficie Celular / Semaforinas / Trastorno del Espectro Autista / Discapacidad Intelectual / Proteínas del Tejido Nervioso Tipo de estudio: Guideline / Prognostic_studies Idioma: En Revista: Pediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article