Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridization*-Reference-Cited by-同舟云学术

Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridization*

Published:2001-05 Issue:5 Volume:16 Page:887-892
ISSN:1460-2350
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Blanco J.,Egozcue J.,Vidal F.

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine

Reference52 articles.

1. Arán, B., Blanco, J., Vidal, F. et al. (1999) Screening for abnormalities of chromosomes X, Y and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program. Fertil. Steril., 72, 696–701.

2. Blanco, J., Egozcue, J. and Vidal, F. (1996) Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization. Hum. Reprod., 11, 722–726.

3. Blanco, J., Rubio, C., Simón, C. et al. (1997) Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH). Hum. Genet., 99, 413–416.

4. Burgoyne, P.S. (1979) Evidence for an association between univalent Y chromosomes and spermatocyte loss in XYY mice and men. Cytogenet. Cell. Genet., 23, 84–89.

5. Burgoyne, P.S, and Biddle, F.G. (1980) Spermatocyte loss in XYY mice. Cytogenet. Cell. Genet., 28, 143–144.

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