Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes?

Pfeiffer, R A; Kändler, C; Sieber, E; Rauch, A; Trautmann, U

Pfeiffer, R A; Kändler, C; Sieber, E; Rauch, A; Trautmann, U.

Affiliation

Pfeiffer RA; Institut für Humangenetik, Erlangen, Germany.

Clin Genet ; 51(5): 357-60, 1997 May.

Article in En | MEDLINE | ID: mdl-9212188

Subject(s)

Chromosomes, Human, Pair 15; Chromosomes, Human, Pair 20; Fingers/abnormalities; Hand Deformities, Congenital/genetics; Translocation, Genetic; Abnormalities, Multiple/genetics; Female; Hand Deformities, Congenital/diagnostic imaging; Humans; Infant; Male; Pedigree; Radiography

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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 15 / Chromosomes, Human, Pair 20 / Hand Deformities, Congenital / Fingers Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Male Language: En Journal: Clin Genet Year: 1997 Document type: Article

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