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Partial uniparental disomy with mosaic deletion 13q in an infant with multiple congenital anomalies.
Jobanputra, V; Wilson, A; Shirazi, M; Feenstra, H; Levy, B; Anyane-Yeboa, K; Warburton, D.
Affiliation
  • Jobanputra V; Department of Pathology, Columbia University, New York, New York 10032, USA. vj2004@columbia.edu
Am J Med Genet A ; 161A(9): 2393-5, 2013 Sep.
Article in En | MEDLINE | ID: mdl-23897564
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 13 / Chromosome Deletion / Uniparental Disomy / Mosaicism Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant Language: En Journal: Am J Med Genet A Year: 2013 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 13 / Chromosome Deletion / Uniparental Disomy / Mosaicism Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant Language: En Journal: Am J Med Genet A Year: 2013 Document type: Article