Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12. | Am J Hum Genet;57(5): 1068-73, 1995 Nov. | MEDLINE

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Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.

Rand, E B; Spinner, N B; Piccoli, D A; Whitington, P F; Taub, R.

Affiliation

Rand EB; Division of Gastroenterology and Nutrition, Children's Hospital of Philadelphia, PA 19104, USA.

Am J Hum Genet ; 57(5): 1068-73, 1995 Nov.

Article in En | MEDLINE | ID: mdl-7485156

Subject(s)

Alagille Syndrome/genetics; Chromosomes, Human, Pair 20; Chromosome Mapping; Female; Gene Deletion; Genotype; Humans; Male; Pedigree

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 20 / Alagille Syndrome Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1995 Document type: Article

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 20 / Alagille Syndrome Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1995 Document type: Article