Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly. | Genet Couns;23(2): 195-200, 2012. | MEDLINE

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Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly.

Chen, C-P; Lin, S-P; Chen, M-R; Su, J-W; Chern, S-R; Chen, Y-J; Lee, M-S; Wang, W.

Affiliation

Chen CP; Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan. cpc_mmh@yahoo.com

Genet Couns ; 23(2): 195-200, 2012.

Article in En | MEDLINE | ID: mdl-22876577

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Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Abnormalities, Multiple / Polydactyly / Cryptorchidism / Heart Defects, Congenital Limits: Child, preschool / Humans / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Country of publication:

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Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Abnormalities, Multiple / Polydactyly / Cryptorchidism / Heart Defects, Congenital Limits: Child, preschool / Humans / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Country of publication: