Homozygosity mapping and Werner's syndrome

The Lancet

Volumn 339, Issue 8799, 1992, Pages 1002-

  Schellenberg, G D ^a   Martin, G M ^a   Wijsman, E M ^a   Nakura, J ^b   Miki, T ^b   Ogihara, T ^b  

^a UNIVERSITY OF WASHINGTON   (United States)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GENE MAPPING; HOMOZYGOSITY; HUMAN; LETTER; PRIORITY JOURNAL; WERNER SYNDROME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 8; HOMOZYGOTE; HUMAN; LOD SCORE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; WERNER SYNDROME;

EID: 0026588296     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/0140-6736(92)91590-5     Document Type: Letter

References (7)

1. Homozygosity mapping. a way to map human recessive traits with the DNA of inbred children
2. Detection of linkage in human genetics
3. Friedreich's Ataxia m Kathikas-Adodhes Cyprus
4. Homozygosity mapping and Friedreich's Ataxia
5. Genetic syndromes m man with potential relevance to the pathobiology of aging
6. Werner's syndrome: a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process
7. Genetic linkage of Werner's syndrome to five markers on chromosome 8