A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.

Weil, D; Portnoï, M F; Levilliers, J; Wang, I; Mathieu, M; Taillemite, J L; Meier, M; Boudailliez, B; Petit, C

Weil, D; Portnoï, M F; Levilliers, J; Wang, I; Mathieu, M; Taillemite, J L; Meier, M; Boudailliez, B; Petit, C.

Affiliation

Weil D; Institut Pasteur, Unité de Génétique Moléculaire Humaine (CNRS URA 1445), Paris, France.

Hum Mol Genet ; 2(11): 1853-6, 1993 Nov.

Article in En | MEDLINE | ID: mdl-8281147

Subject(s)

Chondrodysplasia Punctata/genetics; Translocation, Genetic; Turner Syndrome/genetics; X Chromosome; Y Chromosome; Adolescent; Base Sequence; Chromosome Banding; Chromosome Mapping; DNA/analysis; DNA Primers; Humans; Karyotyping; Male; Molecular Sequence Data; Polymerase Chain Reaction

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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Turner Syndrome / X Chromosome / Y Chromosome / Chondrodysplasia Punctata Limits: Adolescent / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1993 Document type: Article Affiliation country: France Country of publication: United kingdom

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