Exclusion of Autosomal Dominant Polycystic Kidney Disease type II (ADPKD2) from 160 cM of chromosome 1

Shrawan Kumar, William J. Kimberling, Patricia A. Gabow, Yin Y. Shugart, Sandra Pieke-Dahl

Research output: Contribution to journalArticle

Abstract

Autosomal dominant polycystic kidney disease is a heritable disorder and recent studies have shown genetic heterogeneity, with some, but not all, families showing linkage with markers on chromosome 16p. Members of a large ADPKD family, unlinked to chromosome 16, have been typed for 12 marker loci located on both arms of chromosome 1. Multipoint analysis excluded ADPKD2 from the region between D1S81 (pTHH33) and D1S67 (pHHH106) on the long arm and between Rh and PGM1 on the short arm. This excludes the disease locus from about 61% of chromosome 1.

Original languageEnglish (US)
Pages (from-to)697-700
Number of pages4
JournalJournal of Medical Genetics
Volume27
Issue number11
StatePublished - Nov 1990
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Kumar, S., Kimberling, W. J., Gabow, P. A., Shugart, Y. Y., & Pieke-Dahl, S. (1990). Exclusion of Autosomal Dominant Polycystic Kidney Disease type II (ADPKD2) from 160 cM of chromosome 1. Journal of Medical Genetics, 27(11), 697-700.