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Volumn 12, Issue 1, 2001, Pages 95-100

A maternal inherited translocation t(1;22)(q11;p11) in two infertile brothers

Author keywords

Azoospermia; Chromosome 1; Chromosome 22; Infertility; Translocation

Indexed keywords

ADULT; ARTICLE; AZOOSPERMIA; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME 22P; CHROMOSOME TRANSLOCATION 1; CHROMOSOME TRANSLOCATION 22; EXTRACHROMOSOMAL INHERITANCE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; OLIGOSPERMIA; RECIPROCAL CHROMOSOME TRANSLOCATION; SEMEN ANALYSIS; TWINS;

EID: 0035084280     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (15)
  • 2
    • 0022491879 scopus 로고
    • Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the European Collaborative Prenatal Diagnoses Centres
    • (1986) Prenat. Diagn. , vol.6 , pp. 315-350
    • Daniel, A.1    Boue, A.2    Galliano, P.3
  • 5
    • 0028240559 scopus 로고
    • The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions of reproductive fitness II. Robertsonian and reciprocal translocations. An European collaborative study
    • (1984) Ann. Genet. , vol.37 , pp. 3-10
    • Gabriel-Robez, O.1    Rumpler, Y.2
  • 13
    • 0025220142 scopus 로고
    • Prophase of meiosis in human spermatocytes analysed by EM microspreading in infertile men and their controls and comparison with human oocytes
    • (1990) Hum. Genet. , vol.84 , pp. 547-554
    • Speed, R.M.1    Chandley, A.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.