Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy.

Sonmez, Fatma Mujgan; Uctepe, Eyyup; Aktas, Dilek; Alikasifoglu, Mehmet

Sonmez, Fatma Mujgan; Uctepe, Eyyup; Aktas, Dilek; Alikasifoglu, Mehmet.

Afiliação

Sonmez FM; Developmental Child Neurology Association, Ankara, Turkey.
Uctepe E; Department of Medical Genetics, Health Sciences University, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey.
Aktas D; Damagen Genetic Diagnostic Center, Ankara, Turkey.
Alikasifoglu M; Damagen Genetic Diagnostic Center, Ankara, Turkey.

Intractable Rare Dis Res ; 6(1): 61-64, 2017 Feb.

Article em En | MEDLINE | ID: mdl-28357185

Palavras-chave

1q21.3 microdeletion syndrome; developmental delay; mental retardation; microarray-CGH; seizures

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Intractable Rare Dis Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Turquia

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