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Neurologic challenges in 22q11.2 deletion syndrome.
Hopkins, Sarah E; Chadehumbe, Madeline; Blaine Crowley, Terrence; Zackai, Elaine H; Bilaniuk, Larissa T; McDonald-McGinn, Donna M.
Affiliation
  • Hopkins SE; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Chadehumbe M; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Blaine Crowley T; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Bilaniuk LT; Division of Neuroradiology, Children's Hospital of Philadelphia, The University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
  • McDonald-McGinn DM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Am J Med Genet A ; 176(10): 2140-2145, 2018 10.
Article in En | MEDLINE | ID: mdl-30365873
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome / Nervous System Diseases Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2018 Type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome / Nervous System Diseases Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2018 Type: Article