Otopalatodigital syndrome type 2 in a male infant: A case report with a novel sequence variation.

Sankararaman, Senthilkumar; Kurepa, Dalibor; Shen, Yiping; Kakkilaya, Venkatakrishna; Ursin, Sussone; Chen, Harold

Sankararaman, Senthilkumar; Kurepa, Dalibor; Shen, Yiping; Kakkilaya, Venkatakrishna; Ursin, Sussone; Chen, Harold.

Afiliação

Sankararaman S; Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
Kurepa D; Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
Shen Y; Departments of Pathology and Laboratory Medicine, Harvard Medical School, Boston Children's Hospital, Waltham, MA, USA.
Kakkilaya V; Division of Neonatology, Department of Pediatrics, University of South-Western Medical Center, Dallas, TX, USA.
Ursin S; Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
Chen H; Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USA.

J Pediatr Genet ; 2(1): 33-6, 2013 Mar.

Article em En | MEDLINE | ID: mdl-27625837

Palavras-chave

FLNA gene; Otopalatodigital syndrome type 2; filamin A

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Pediatr Genet Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Estados Unidos

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