Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report.

Traylor, Ryan N; Fan, Zheng; Hudson, Beth; Rosenfeld, Jill A; Shaffer, Lisa G; Torchia, Beth S; Ballif, Blake C

Traylor, Ryan N; Fan, Zheng; Hudson, Beth; Rosenfeld, Jill A; Shaffer, Lisa G; Torchia, Beth S; Ballif, Blake C.

Afiliação

Traylor RN; Signature Genomic Laboratories, Spokane, WA, USA. ballif@signaturegenomics.com.

Mol Cytogenet ; 2: 17, 2009 Aug 07.

Article em En | MEDLINE | ID: mdl-19664229

Texto completo

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731778
https://dx.doi.org/10.1186/1755-8166-2-17

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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Mol Cytogenet Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos