Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping

American Journal of Human Genetics

Volumn 61, Issue 6, 1997, Pages 1335-1341

  Neufeld, Ellis J ^a   Mandel, Hanna ^c   Raz, Tal ^c   Szargel, Raymonde ^c   Yandava, Chandri N ^b   Stagg, Amy ^a   Fauré, Sabine ^d   Barrett, Timothy ^e   Buist, Neil ^f   Cohen, Nadine ^c  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^d GÉNÉTHON   (France)

^e UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^f OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; THIAMINE;

ARTICLE; CHROMOSOME 1Q; CONTROLLED STUDY; DIABETES MELLITUS; FEMALE; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HAPLOTYPE; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; ISRAEL; ITALY; MAJOR CLINICAL STUDY; MALE; MEGALOBLASTIC ANEMIA; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SYNDROME; UNITED STATES;

EID: 17344368928     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301642     Document Type: Article

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