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Trisomy 18q: 46,XX,-10,+der(10) t(10;18) (p15;q12) pat: a case report.
Murthy, S K; Kar, B; Prabhakara, K; Krishnamurthy, D S.
Affiliation
  • Murthy SK; Department of Zoology, University School of Sciences, Gujarat University, Ahmedabad, India.
Ann Genet ; 35(3): 174-7, 1992.
Article in En | MEDLINE | ID: mdl-1466569
ABSTRACT
A 2-month-old female with intrauterine and postnatal growth retardation, multiple congenital anomalies, absent right kidney, congenital heart disease was investigated. Her karyotype revealed, 46,XX,-10,+der(10), t(10;18) (p15;q12) pat. The child died at 2 months 2 weeks. This is the third case of trisomy 18q resulting from translocation of chromosome 10 and 18.
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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Trisomy / Abnormalities, Multiple / Chromosomes, Human, Pair 10 / Chromosomes, Human, Pair 18 Limits: Female / Humans / Infant Language: En Journal: Ann Genet Year: 1992 Document type: Article Affiliation country: India
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Trisomy / Abnormalities, Multiple / Chromosomes, Human, Pair 10 / Chromosomes, Human, Pair 18 Limits: Female / Humans / Infant Language: En Journal: Ann Genet Year: 1992 Document type: Article Affiliation country: India