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Volumn 117 A, Issue 2, 2003, Pages 122-126

Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: Confirmation and refinement of the DFNA25 locus

(7) Petek, Erwin a Windpassinger, Christian a Mach, Monika a Rauter, Ludwig b Scherer, Stephen W c Wagner, Klaus a Kroisel, Peter M a

a UNIVERSITY OF GRAZ (Austria)

b Leoben Hospital (Austria)

c HOSPITAL FOR SICK CHILDREN (Canada)

Author keywords

12q; Deafness; Deletion; DFNA25; DFNA41; Microsatellite markers, YAC

Indexed keywords

GENOMIC DNA; MICROSATELLITE DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 12Q; CHROMOSOME DELETION; CONGENITAL DEAFNESS; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; KARYOTYPE; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME; CHILD; CHROMOSOME 12; CHROMOSOME BANDING PATTERN; CHROMOSOME MAP; DOMINANT GENE; FAMILY HEALTH; FEMALE; GENETICS; GENOTYPE; HEARING LOSS; METHODOLOGY; PATHOLOGY; PEDIGREE;

CHILD; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENOTYPE; HEARING LOSS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROSATELLITE REPEATS; PEDIGREE;

EID: 0042279177 PISSN: 15524825 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.a.10155 Document Type: Article

Times cited : (20)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.