Chromosome abnormalities in sperm from infertile men with asthenoteratozoospermia

Biology of Reproduction

Volumn 66, Issue 6, 2002, Pages 1781-1783

  Hristova, Rositsa ^a   Ko, Evelyn ^a   Greene, Calvin ^a   Rademaker, Alfred ^a   Chernos, Judy ^a   Martin, Renée ^a  

^a ALBERTA CHILDREN'S HOSPITAL   (Canada)

Author keywords

Assisted reproductive technology; Sperm; Sperm motility and transport; Spermatogenesis

Indexed keywords

ADULT; ARTICLE; ASTHENOSPERMIA; CHROMOSOME 13; CHROMOSOME 21; CHROMOSOME ABERRATION; CONTROLLED STUDY; DIPLOIDY; DISOMY; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; INTRACYTOPLASMIC SPERM INJECTION; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MALE; MALE INFERTILITY; PRIORITY JOURNAL; SEMEN ANALYSIS; SPERMATOZOON MOTILITY; CONGENITAL MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; MIDDLE AGED; SEX CHROMOSOME ABERRATION; SPERMATOZOON; ULTRASTRUCTURE; X CHROMOSOME; Y CHROMOSOME;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFERTILITY, MALE; MALE; MIDDLE AGED; SEX CHROMOSOME ABERRATIONS; SPERM MOTILITY; SPERMATOZOA;

EID: 0035988228     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod66.6.1781     Document Type: Article

References (23)

1. Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in-situ hybridization
2. The risk of chromosomal abnormalities following ICSI
3. Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men
4. Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization
5. Incidence of aneuploid spermatozoa among infertile men studied by multicolour fluorescence in-situ hybridization
6. Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males
7. 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
8. A 47, XXY fetus resulting from ICSI in a man with an elevated frequency of 24,XY sperm
9. Chromosome 21 disomy in spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down Syndrome: Increased incidence in cases of paternal origin
10. Analysis of sex chromosome aneuploidy in sperm from fathers of Turner Syndrome patients
11. Incidence of chromosomal aberrations in children born after assisted reproduction through intracytoplasmic sperm injection
12. Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection
13. Case report: Paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI)
14. Paternal age effect of YY aneuploidy in human sperm, as assessed by fluorescence in-situ hybridization
15. Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human sperm using multicolour FISH
16. Cloning of human satellite III DNA: Different components are on different chromosomes
17. Macromolecular organization of human centromeric regions reveals high-frequency, polymorphic macro DNA repeats
18. Methods for comparing event rates in intervention studies when the unit of allocation is a cluster
19. Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoaesthenoterato-zoospermia undergoing intracytoplasmic sperm injection
20. Human male infertility: Chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion
21. Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in situ hybridization in infertile men