SCOPUS 정보 검색 플랫폼

Volumn 108, Issue 5, 2001, Pages 385-389

Connexin 26 (GJB2) mutations in the Turkish population: Implications for the origin and high frequency of the 35delG mutation in Caucasians

(8) Tekin, M a Akar, N a Cin, S a Blanton, S H a Xia, X J a Liu, X Z a Nance, W E a Pandya, A a

a VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26;

ALLELE; ARTICLE; CAUCASIAN; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; FOUNDER EFFECT; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC SCREENING; GENETIC VARIABILITY; HAPLOTYPE; HEARING IMPAIRMENT; HETEROZYGOTE DETECTION; HUMAN; PEDIGREE ANALYSIS; PREVALENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TURKEY (REPUBLIC); UNITED STATES;

ALLELES; CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; FOUNDER EFFECT; GENE FREQUENCY; HAPLOTYPES; HETEROZYGOTE; HUMANS; MALE; MICROSATELLITE REPEATS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; SEQUENCE DELETION; TURKEY; UNITED STATES;

EID: 0035000818 PISSN: 03406717 EISSN: None Source Type: Journal
DOI: 10.1007/s004390100507 Document Type: Article

Times cited : (65)

References (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.