Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.

Turner, G; Gedeon, A; Mulley, J; Sutherland, G; Rae, J; Power, K; Arthur, I

Turner, G; Gedeon, A; Mulley, J; Sutherland, G; Rae, J; Power, K; Arthur, I.

Affiliation

Turner G; Department of Medical Genetics, Prince of Wales Children's Hospital, Sydney, Australia.

Am J Med Genet ; 34(4): 463-9, 1989 Dec.

Article in En | MEDLINE | ID: mdl-2624253

Subject(s)

Abnormalities, Multiple/genetics; Genetic Linkage; Intellectual Disability/genetics; X Chromosome; Adolescent; Adult; Child, Preschool; Chromosome Mapping; Female; Genes, Recessive; Genotype; Humans; Infant; Lod Score; Male; Pedigree; Phenotype; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Abnormalities, Multiple / Genetic Linkage / Intellectual Disability Limits: Adolescent / Adult / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Am J Med Genet Year: 1989 Type: Article Affiliation country: Australia

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