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Volumn 88, Issue 2, 2015, Pages 177-181

Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population
[No Author Info available]

Author keywords

Ashkenazi Jewish; Carrier screening; Dyskeratosis congenita; Hoyeraal Hreidarsson syndrome; RTEL1

Indexed keywords

ADULT; ARTICLE; ASHKENAZI JEW; CONTROLLED STUDY; DYSKERATOSIS CONGENITA; GENE; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE; GERMLINE MUTATION; HAPLOTYPE; HETEROZYGOTE; HOYERAAL HREIDARSSON SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MUTATION RATE; PRIORITY JOURNAL; RTEL1 GENE; DNA SEQUENCE; FEMALE; FETAL GROWTH RETARDATION; GENETICS; HETEROZYGOTE DETECTION; IMMUNE DEFICIENCY; INTELLECTUAL DISABILITY; JEW; MALE; MICROCEPHALY; NUCLEOTIDE SEQUENCE; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84935746915     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12459     Document Type: Article
Times cited : (16)

References (17)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.