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Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephaly.
Abdel-Hamid, Mohamed S; El-Dessouky, Sara H; Ateya, Mohamed I; Gaafar, Hassan M; Abdel-Salam, Ghada M H.
Affiliation
  • Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • El-Dessouky SH; Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Ateya MI; Fetal Medicine Unit, Cairo University, Cairo, Egypt.
  • Gaafar HM; Fetal Medicine Unit, Cairo University, Cairo, Egypt.
  • Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Am J Med Genet A ; 179(3): 494-497, 2019 03.
Article in En | MEDLINE | ID: mdl-30637988
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetic Predisposition to Disease / Genetic Association Studies / Hydranencephaly / Microcephaly / Microtubule-Associated Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Egypt
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetic Predisposition to Disease / Genetic Association Studies / Hydranencephaly / Microcephaly / Microtubule-Associated Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Egypt