SCOPUS 정보 검색 플랫폼

Volumn 111, Issue 4, 2002, Pages 443-445

Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23 [2]

(6) De Vries, Bert B A a,b Breedveld, Guido J a Deelen, Wouter H a Breuning, Martijn H c Niermeijer, Martinus F a Heutink, Peter a

a ERASMUS MEDICAL CENTER (Netherlands)

b RADBOUD UNIVERSITY MEDICAL CENTER (Netherlands)

c LEIDEN UNIVERSITY MEDICAL CENTER (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME MAP; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HAPLOTYPE; HUMAN; LETTER; LINKAGE ANALYSIS; MALE; MENTAL DEFICIENCY; PEDIGREE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE; GENETIC RECOMBINATION; GENETICS; X CHROMOSOME; X LINKED MENTAL RETARDATION;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, X; FEMALE; HAPLOTYPES; HUMAN; MALE; MENTAL RETARDATION, X-LINKED; PEDIGREE; RECOMBINATION, GENETIC; HUMANS;

EID: 0036707806 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10576 Document Type: Letter

Times cited : (5)

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