Concepedia

Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

Herbert Schuster, Thomas F. Wienker, Sylvia Bähring, N Bilginturan, Hakan R. Toka, Heidemarie Neitzel, Eva Jeschke, Okan Toka, Dennis A. Gilbert, Adam J. Lowe,

Nature Genetics · 1996 · 145 citations · 15 references

DOI

Concepts

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15

The Metabolic Basis of Inherited Disease

Annals of Internal Medicine · 1990 · 4K citations

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Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

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Faster sequential genetic linkage computations.

Robert W. Cottingham, Ramana M. Idury, Alejandro A. Schäffer · PubMed · 1993 · 1.4K citations

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Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel

Richard A. Shimkets, David G. Warnock, Christopher M. Bositis et al. · Cell · 1994 · 1.3K citations

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A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

Richard P. Lifton, Robert G. Dluhy, Michael D. Powers et al. · Nature · 1992 · 1.2K citations · Full text

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