A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome.

Udayakumar, Achandira M; Al-Kindy, Adila

Udayakumar, Achandira M; Al-Kindy, Adila.

Afiliação

Udayakumar AM; Cytogenetics Unit, Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Sultanate Oman.
Al-Kindy A; Clinical Genetics Unit, Department of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University, Muscat, Sultanate Oman.

J Pediatr Genet ; 2(3): 141-6, 2013 Sep.

Article em En | MEDLINE | ID: mdl-27625852

Palavras-chave

18p- syndrome; de Grouchy syndrome; monosomy 18p syndrome; mosaic 18p-/i(18q) syndrome; trisomy 18q syndrome

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Pediatr Genet Ano de publicação: 2013 Tipo de documento: Article

Texto completo

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PubMed Links

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Pediatr Genet Ano de publicação: 2013 Tipo de documento: Article