Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1

British Journal of Dermatology

Volumn 165, Issue 1, 2011, Pages 201-203

  Parren, L J M T ^c,d   Abuzahra, F ^a,b   Wagenvoort, T ^c   Koene, F ^c   Van Steensel, M A M ^c,d   Steijlen, P M ^c,d   Van Geel, M ^c,d   Frank, J ^c,d  

^a UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^b ZAANS MEDICAL CENTER   (Netherlands)

^c MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^d MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BAZEX DUPRE CHRISTOL SYNDROME; CHROMOSOME XQ; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENODERMATOSIS; HAPLOTYPE; HUMAN; LETTER; MALE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SYNDROME; SYNDROME DELINEATION;

ANEURYSM; CARCINOMA, BASAL CELL; CHROMOSOMES, HUMAN, X; FAMILY; GENETIC LINKAGE; HAPLOTYPES; HISTIOCYTOMA, BENIGN FIBROUS; HUMANS; HYPOTRICHOSIS; PEDIGREE; SKIN NEOPLASMS;

EID: 79959711220     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2011.10219.x     Document Type: Letter

References (10)

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