Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: Case report

Human Reproduction

Volumn 20, Issue 8, 2005, Pages 2168-2172

  Brisset, Sophie ^a   Izard, V ^b   Misrahi, M ^b   Aboura, A ^a   Madoux, S ^a   Ferlicot, S ^b   Schoevaert, D ^b   Soufir, J C ^b   Frydman, R ^a   Tachdjian, G ^a  

^a HÔPITAL ANTOINE BÉCLÈRE   (France)

^b BICÊTRE HOSPITAL   (France)

Author keywords

(Y; autosome) translocation; AZF deletions; Azoospermia; Genotype phenotype correlation; Testicular biopsy

Indexed keywords

ADULT; ARTICLE; AZOOSPERMIA; CASE REPORT; CENTROMERE; CHROMOSOME ARM; CHROMOSOME TRANSLOCATION 22; CHROMOSOME TRANSLOCATION Y; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE PHENOTYPE CORRELATION; HETEROCHROMATIN; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE 45,X; LYMPHOCYTE; MALE; MALE INFERTILITY; METAPHASE; MOLECULAR DYNAMICS; SEX CHROMOSOME MOSAICISM; TESTIS; CHROMOSOME 22; GENE TRANSLOCATION; GENETICS; GENOTYPE; OLIGOSPERMIA; PATHOLOGY; PHENOTYPE; SPERMATOZOON; Y CHROMOSOME;

ADULT; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, Y; GENOTYPE; HUMANS; MALE; OLIGOSPERMIA; PHENOTYPE; SPERMATOZOA; TESTIS; TRANSLOCATION, GENETIC;

EID: 25144465146     PISSN: 02681161     EISSN: 14602350     Source Type: Journal    
DOI: 10.1093/humrep/dei034     Document Type: Article

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