Facilitated diagnosis of the contiguous gene syndrome: Tuberous sclerosis and polycystic kidneys by means of haplotype studies

American Journal of Kidney Diseases

Volumn 31, Issue 6, 1998, Pages 1038-1043

  Torra, Roser ^a   Badenas, Cèlia ^b   Darnell, Alejandro ^b   Camacho, Juan Antonio ^b   Aspinwall, Richard ^b   Harris, Peter C ^b   Estivill, Xavier ^b  

^a HOSPITAL CLÍNIC   (Spain)

^b NONE

Author keywords

Contiguous gene syndrome children; Deletion; Genetics; Loss of heterozigosity; Microsatellites; Polycysttc kidneys; Tuberous sclerosis type 2

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 16P; DISEASE ASSOCIATION; FEMALE; GENE ISOLATION; HAPLOTYPE; HETEROZYGOSITY LOSS; HUMAN; INFANT; KIDNEY POLYCYSTIC DISEASE; TUBEROUS SCLEROSIS;

EID: 0031778645     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/ajkd.1998.v31.pm9631851     Document Type: Article

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