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Volumn 7, Issue 3, 2012, Pages

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure

(14)  Caburet, Sandrine a,b   Zavadakova, Petra c,j   Ben Neriah, Ziva d   Bouhali, Kamal e   Dipietromaria, Aurélie e   Charon, Céline f   Besse, Céline f   Laissue, Paul g,k,l   Chalifa Caspi, Vered h   Christin Maitre, Sophie i   Vaiman, Daniel g   Levi, Giovanni e   Veitia, Reiner A a,b   Fellous, Marc g  

f DIF   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 7P; CHROMOSOME 7Q; CLINICAL ARTICLE; CONSANGUINITY; DLX5 GENE; DLX6 GENE; DSS1 GENE; FAMILIAL DISEASE; FEMALE; GENE; GENE IDENTIFICATION; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; PREMATURE OVARIAN FAILURE; ARAB; CASE REPORT; CHROMOSOME 7; DNA SEQUENCE; GENE LOCUS; GENETICS; PEDIGREE;

EID: 84858141201     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0033412     Document Type: Article
Times cited : (28)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.