Human chromosome 17 in essential hypertension

Annals of Human Genetics

Volumn 67, Issue 2, 2003, Pages 193-206

  Knight, J ^a   Munroe, P B ^a   Pembroke, J C ^a   Caulfield, M J ^a  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIPORTER; DIPEPTIDYL CARBOXYPEPTIDASE; PHENYLETHANOLAMINE N METHYLTRANSFERASE;

CHROMOSOME 10; CHROMOSOME 17; COMPARATIVE GENE MAPPING; DIASTOLIC BLOOD PRESSURE; ESSENTIAL HYPERTENSION; GENE IDENTIFICATION; GENETIC LINKAGE; GENETIC RISK; GENETIC SCREENING; GENETIC TRAIT; HUMAN; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM; QUANTITATIVE TRAIT LOCUS; RAT; REVIEW; RISK FACTOR; SYSTOLIC BLOOD PRESSURE; ANIMAL; BLOOD PRESSURE; CHROMOSOME MAP; DISEASE MODEL; GENETIC MARKER; GENETICS; HYPERTENSION; SPONTANEOUSLY HYPERTENSIVE RAT; ULTRASTRUCTURE;

RODENTIA;

ANIMALS; BLOOD PRESSURE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DISEASE MODELS, ANIMAL; GENETIC MARKERS; HUMANS; HYPERTENSION; LINKAGE (GENETICS); MICE; PEPTIDYL-DIPEPTIDASE A; PHENOTYPE; PSEUDOHYPOALDOSTERONISM; QUANTITATIVE TRAIT LOCI; RATS; RATS, INBRED SHR;

EID: 0141889546     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-1809.2003.t01-1-00002.x     Document Type: Review

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