Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia

Archives of Andrology

Volumn 52, Issue 4, 2006, Pages 263-267

  Samli, Hale ^a   Samli, M M ^a   Solak, M ^a   Imirzalioglu, N ^b  

^a AFYON KOCATEPE UNIVERSITY   (Turkey)

^b SULEYMAN DEMIREL UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

Author keywords

Azoospermia; Genetics; Karyotype; Oligozoospermia

Indexed keywords

FOLLITROPIN; TESTOSTERONE;

ADULT; ARTICLE; AZOOSPERMIA; CYTOGENETICS; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC DISORDER; GENETIC RISK; HIGH RISK PATIENT; HUMAN; INFERTILITY THERAPY; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; NUMERICAL CHROMOSOME ABERRATION; OLIGOSPERMIA; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; CHROMOSOME ABERRATION; CONGENITAL MALFORMATION; GENETICS; KLINEFELTER SYNDROME; MOSAICISM; RETROSPECTIVE STUDY;

ABNORMALITIES; CHROMOSOME ABERRATIONS; HUMANS; INFERTILITY, MALE; KLINEFELTER SYNDROME; MALE; MOSAICISM; OLIGOSPERMIA; RETROSPECTIVE STUDIES;

EID: 33746924903     PISSN: 01485016     EISSN: 15210375     Source Type: Journal    
DOI: 10.1080/01485010600664032     Document Type: Article

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