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Volumn 26, Issue 4, 2009, Pages 427-430
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Genetic defect in Chinese azoospermic patients and their relationship with reproductive hormones
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Author keywords
Azoospermia; Karyotype analysis; Reproductive hormone; Y chromosome microdeletion
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Indexed keywords
FOLLITROPIN;
LUTEINIZING HORMONE;
PROLACTIN;
TESTOSTERONE;
ARTICLE;
AZOOSPERMIA;
CHEMOLUMINESCENCE;
CHINESE;
CHROMOSOME ABERRATION;
CONTROLLED STUDY;
DISEASE ASSOCIATION;
FOLLITROPIN BLOOD LEVEL;
GENE DELETION;
GENETIC DISORDER;
HUMAN;
IMMUNOASSAY;
KARYOTYPE;
KLINEFELTER SYNDROME;
LUTEINIZING HORMONE BLOOD LEVEL;
MAJOR CLINICAL STUDY;
MALE;
MALE FERTILITY;
MULTIPLEX POLYMERASE CHAIN REACTION;
PROLACTIN BLOOD LEVEL;
PROMOTER REGION;
SEX CHROMOSOME ABERRATION;
TESTOSTERONE BLOOD LEVEL;
Y CHROMOSOME;
ADULT;
AZOOSPERMIA;
CASE-CONTROL STUDIES;
CHROMOSOMES, HUMAN, Y;
FOLLICLE STIMULATING HORMONE;
GENETIC ASSOCIATION STUDIES;
HUMANS;
KARYOTYPING;
LUTEINIZING HORMONE;
MALE;
PROLACTIN-RELEASING HORMONE;
SEMINAL PLASMA PROTEINS;
SEQUENCE DELETION;
TESTOSTERONE;
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EID: 69249122135
PISSN: 10039406
EISSN: None
Source Type: Journal
DOI: 10.3760/cma.j.issn.1003-9406.2009.04.014 Document Type: Article |
Times cited : (4)
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References (7)
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