Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).

Chen, C P; Lin, S P; Lin, C C; Li, Y C; Hsieh, L J; Huang, J K; Lee, C C; Wang, W

Chen, C P; Lin, S P; Lin, C C; Li, Y C; Hsieh, L J; Huang, J K; Lee, C C; Wang, W.

Affiliation

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

Genet Couns ; 17(1): 57-63, 2006.

Article de En | MEDLINE | ID: mdl-16719278

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Collection: 01-internacional Base de données: MEDLINE Sujet principal: Trisomie / Chromosomes humains de la paire 7 / Chromosomes humains de la paire 12 / Syndrome de Dandy-Walker / Monosomie Type d'étude: Prognostic_studies Limites: Child / Humans / Male Langue: En Journal: Genet Couns Sujet du journal: ETICA / GENETICA MEDICA Année: 2006 Type de document: Article Pays d'affiliation: Chine

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