Alström syndrome: further evidence for linkage to human chromosome 2p13.

Collin, G B; Marshall, J D; Boerkoel, C F; Levin, A V; Weksberg, R; Greenberg, J; Michaud, J L; Naggert, J K; Nishina, P M

Collin, G B; Marshall, J D; Boerkoel, C F; Levin, A V; Weksberg, R; Greenberg, J; Michaud, J L; Naggert, J K; Nishina, P M.

Affiliation

Collin GB; The Jackson Laboratory, Bar Harbor, ME 04609-1500, USA.

Hum Genet ; 105(5): 474-9, 1999 Nov.

Article in En | MEDLINE | ID: mdl-10598815

Subject(s)

Chromosomes, Human, Pair 2/genetics; Diabetes Mellitus, Type 2/genetics; Genetic Linkage; Hearing Loss, Sensorineural/genetics; Obesity/genetics; Retinal Degeneration/genetics; Base Sequence; Chromosome Mapping; DNA Primers/genetics; Female; Genes, Recessive; Genetic Markers; Humans; Lod Score; Male; Pedigree; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Retinal Degeneration / Chromosomes, Human, Pair 2 / Diabetes Mellitus, Type 2 / Hearing Loss, Sensorineural / Genetic Linkage / Obesity Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 1999 Type: Article Affiliation country: United States

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