Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males

Human Genetics

Volumn 105, Issue 3, 1999, Pages 266-272

  Rives, Nathalie ^a   Saint Clair, Alexia ^a   Mazurier, Sophie ^a   Sibert, Louis ^a   Siméon, Nathalie ^a   Joly, Géraldine ^a   Macé, Bertrand ^a  

^a HÔPITAL CHARLES NICOLLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; AUTOSOME; CELL NUCLEUS; CELL STRUCTURE; CHROMOSOME 1; CHROMOSOME 13; CHROMOSOME 14; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME PAIRING; CLINICAL EXAMINATION; CONTROLLED STUDY; DISOMY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPING; LYMPHOCYTE; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; MEIOSIS; OLIGOSPERMIA; PHENOTYPE; PRIORITY JOURNAL; SPERM; SPERMATOGENESIS; SPERMATOZOON COUNT; SPERMATOZOON MOTILITY; ULTRASOUND; X CHROMOSOME; Y CHROMOSOME;

ADULT; ANEUPLOIDY; CELL NUCLEUS; DATA INTERPRETATION, STATISTICAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFERTILITY, MALE; MALE; MIDDLE AGED; PHENOTYPE; SEMEN; SPERM COUNT; SPERM MOTILITY; SPERMATOZOA;

EID: 0032861094     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051100     Document Type: Article

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