SCOPUS 정보 검색 플랫폼

Somatic Cell and Molecular Genetics

Volumn 13, Issue 3, 1987, Pages 285-292

Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively

(5) Royle, N J a Irwin, D M b Koschinsky, M L b MacGillivray, R T A b Hamerton, J L c

a UNIVERSITY OF LEICESTER (United Kingdom)

b UNIVERSITY OF BRITISH COLUMBIA (Canada)

c UNIVERSITY OF MANITOBA (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR; CERULOPLASMIN; PROTHROMBIN;

BLOOD AND HEMOPOIETIC SYSTEM; CHROMOSOME 11P; CHROMOSOME 3Q; DNA PROBE; GENE ASSIGNMENT; GENE LOCATION; GENE MAPPING; GENETIC ENGINEERING; HEREDITY; HUMAN; HUMAN CELL; HYBRID CELL; IN SITU HYBRIDIZATION; IN VITRO STUDY; NORMAL HUMAN; NORMAL VALUE;

CERULOPLASMIN; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 3; DNA; DNA, RECOMBINANT; GENES; HUMANS; NUCLEIC ACID HYBRIDIZATION; PROTHROMBIN;

EID: 0023175705 PISSN: 07407750 EISSN: 15729931 Source Type: Journal
DOI: 10.1007/BF01535211 Document Type: Article

Times cited : (95)

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