Narrowing the position of the Werner syndrome locus by homozygosity analysis - Extension of homozygosity analysis

Genomics

Volumn 36, Issue 1, 1996, Pages 130-141

  Nakura, Jun ^a   Miki, Tetsuro ^a   Ye, L ^a   Mitsuda, Noriaki ^a   Zhao, Yi ^a   Kihara, Koichi ^a   Yu, Chang En ^b   Oshima, Junko ^b   Fukuchi, Ken Ichiro ^b,g   Wijsman, Ellen M ^c   Schellenberg, Gerard D ^b   Martin, George M ^b   Murano, Shun Ichi ^d   Hashimoto, Katsuyuki ^e   Fujiwara, Yosisada ^f   Ogihara, Toshio ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b UNIVERSITY OF WASHINGTON   (United States)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^d CHIBA UNIVERSITY   (Japan)

^e NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^f KOBE UNIVERSITY   (Japan)

^g NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; GENE LOCUS; GENE MAPPING; GENOTYPE; HOMOZYGOSITY; HUMAN; HUMAN CELL; PRIORITY JOURNAL; WERNER SYNDROME;

MARTES PENNANTI;

EID: 0030586959     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0433     Document Type: Article

References (49)

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