Chromosomal alterations and male infertility
- 1 November 2000
- journal article
- research article
- Published by Springer Nature in Journal of Endocrinological Investigation
- Vol. 23 (10) , 677-683
- https://doi.org/10.1007/bf03343793
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- XY-quadrivalent association and sterility in a man carrier of a reciprocal autosomal translocation involving the whole arm of an acrocentric chromosome t(2;15)(q21.3;cen)Andrologia, 2009
- The meiotic checkpoint monitoring sypapsis eliminates spermatocytes via p53-independent apoptosisNature Genetics, 1998
- Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH)Human Genetics, 1997
- Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formationHuman Molecular Genetics, 1996
- Population studies of inv(9) chromosomes in 4,300 japanese: Incidence, sex difference and clinical significanceJournal of Human Genetics, 1992
- The frequencies of constitutional chromosome abnormalities in an apparently normal adult populationMutation Research Letters, 1992
- Pericentric inversion in human chromosome 1 and the risk for male sterility.Journal of Medical Genetics, 1987
- Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: A large prenatal studyAmerican Journal of Medical Genetics, 1987
- Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterilityCytogenetic and Genome Research, 1985
- Evidence for an association between univalent Y chromosomes and spermatocyte loss in XYY mice and menCytogenetic and Genome Research, 1979