Refined localization of dyschromatosis symmetrica hereditaria gene to a 9·4-cM region at 1q21-22 and a literature review of 136 cases reported in China

British Journal of Dermatology

Volumn 150, Issue 4, 2004, Pages 633-639

  He, P P ^a,b   He, C D ^c   Cui, Y ^a   Yang, S ^a   Xu, H H ^c   Li, M ^a   Yuan, W T ^b   Gao, M ^a   Liang, Y H ^a   Li, C R ^a   Xu, S J ^b   Chen, J J ^a   Chen, H D ^c   Huang, W ^b   Zhang, X J ^a  

^a ANHUI MEDICAL UNIVERSITY   (China)

^b CHINESE NATIONAL HUMAN GENOME CENTER AT SHANGHAI   (China)

^c CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Dyschromatosis symmetrica hereditaria; Genotyping; Haplotype analysis; Hyperpigmented and hypopigmented macules; Linkage analysis; Literature review

Indexed keywords

MARKER;

CHINA; CHROMOSOME 1Q; CLINICAL FEATURE; DISEASE ACTIVITY; DISEASE COURSE; DNA POLYMORPHISM; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; FAMILY; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; GENODERMATOSIS; GENOTYPE; HAPLOTYPE; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; JAPAN; MICROSATELLITE MARKER; NECK; PRIORITY JOURNAL; REVIEW; SCORING SYSTEM; SKIN DEFECT; THORAX;

ADULT; CHINA; CHROMOSOMES, HUMAN, PAIR 1; FAMILY HEALTH; FEMALE; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIDDLE AGED; PEDIGREE; PIGMENTATION DISORDERS;

EID: 2342461705     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0007-0963.2004.05861.x     Document Type: Review

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