Study of the occurrence of interchromosomal effect in spermatozoa of chromosomal rearrangement carriers by fluorescence in-situ hybridization and primed in-situ labelling techniques

Human Reproduction

Volumn 16, Issue 6, 2001, Pages 1155-1164

  Pellestor, Franck ^a   Imbert, Isabelle ^a   Andréo, Brigitte ^a   Lefort, Geneviève ^b  

^a INSTITUTE OF HUMAN GENETICS   (France)

^b HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

FISH; Interchromosomal effect; PRINS; Rearrangement; Spermatozoa

Indexed keywords

ADULT; ANALYTICAL PARAMETERS; ANEUPLOIDY; ARTICLE; CHROMOSOME 1; CHROMOSOME 13; CHROMOSOME 15; CHROMOSOME 20; CHROMOSOME 21; CHROMOSOME 4; CHROMOSOME 9; CHROMOSOME REARRANGEMENT; CHROMOSOME SEGREGATION; CHROMOSOME STRUCTURE; CONTROLLED STUDY; CYTOGENETICS; DIPLOIDY; DISOMY; FLUORESCENCE IN SITU HYBRIDIZATION; GAMETE; GENETIC COUNSELING; HETEROZYGOTE; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MALE FERTILITY; MALE INFERTILITY; MEIOSIS; NONDISJUNCTION; PRIMED IN SITU LABELING; SEGREGATION ANALYSIS; SEMEN ANALYSIS; SEX CHROMOSOME; SPERMATOZOON; X CHROMOSOME; Y CHROMOSOME;

EID: 0034969830     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/16.6.1155     Document Type: Article

References (53)

1. Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1) (q32 ;q42): Regular loop formation but defective synapsis including a possible interchromosomal effect
2. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization
3. FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: Results in a translocation carrier, t(5;8) (q33;q13)
4. Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei
5. Genome-wide variation in recombination in female meiosis: A risk factor for non-disjunction of chromosome 21
6. Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the humster in vitro penetration system
7. Two cases of familial paracentric inversion in man associated with sex chromosome anomaly 47,XXY,inv(5) (q21q32) and 45,X,inv(7) (q11.3q22.3)
8. An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization
9. Cytogenetic analysis of sperm chromosomes and sperm nuclei in a male heterozygous for a reciprocal translocation t(5;7) (q21;q32) by in situ hybridization
10. Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9) (p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei
11. Primed in situ (PRINS) labeling with Alu and satellite primers for rapid characterization of human chromosomes in hybrid cell lines
12. Structural rearrangements in the parents of children with primary trisomy 21
13. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies
14. Sperm analysis in a subfertile male with a Y;16 translocation, using four color FISH
15. Meiotic analysis by FISH of a human male 46,XY,t(15;20) (q11.2;q11.2) translocation heterozygote: Quadrivalent configuration, orientation and first meiotic segregation
16. A new hypothesis on the nature and sequence of meiotic events in the female of Drosophila melanogaster
17. Three dimensional reconstruction of human pachytene spermatocyte nuclei of a 17;21 reciprocal translocation carrier: Study of XY-autosome relationships
18. Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization
19. Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review
20. Interchromosomal effect in man
21. Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9) (q26.2;q32) and t(3;9) (p25;q32), by triple-color fluorescence in situ hybridization
22. Analysis of chromosome behavior in intact mammalian oocytes: Monitoring the segregation of a univalent chromosome during female meiosis
23. Sex chromosomal abnormalities and intracytoplasmic sperm injection
24. The chromosome complement of human gametes
25. Lack of checkpoint control at the metaphase/anaphase transition: A mechanism of meiotic nondisjunction in mammalian females
26. Autosomal disorders
27. Meiosis: How could it work?
28. The prevalence of translocations in parents of children with regular trisomy 21: A possible interchromosomal effect?
29. Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8) (q23;q27;p21)
30. Pachytene analysis of a man with a 13q;14q translocation and infertility
31. Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46, XY,t(9;13) (q21.1;q21.2) and a review of the literature
32. Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11) (q27.3;q24.3) by triple FISH
33. Molecular analysis of the chromosomal equipment in spermatozoa of a 46,XY,t(7;8) (q11.21;cen) carrier by using fluorescence in situ hybridization
34. Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization
35. Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization
36. Chromosome analysis in human oocytes remaining unfertilized after in-vitro insemination: Effect of maternal age and fertilization rate
37. XY-trivalent association and synaptic anomalies in a male carrier of a Robertsonian t(13;14) translocation
38. Differential distribution of aneuploidy in human gametes according to their sex
39. Assessment of aneuploidy for chromosomes 8, 9, 13, 16 and 21 in human sperm by using Primed In Situ labeling technique
40. Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques
41. Further studies on the interchromosomal effect on crossing over in Drosophila melanogaster affecting the preconditions of exchange
42. Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of infertile male
43. Detection of aneuploid human sperm fluorescence in situ hybridization: Evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y
44. Sperm nuclei analysis of a Robertsonian t(14q21q) carrier by FISH using three plasmids and two YAC probes
45. Meiotic segregation in males heterozygote for reciprocal translocations: Analysis of sperm nuclei by two and three colour flourescence in situ hybridization
46. Direct analysis of the chromosome constitution of human spermatozoa
47. No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements
48. Pericentric inversion of chromosome 9: Prevalence in 300 Down syndrome families and molecular studies of nondisjunction
49. Aneuploidy in human sperm: Results of two and three color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X and Y
50. Aneuploidy in human sperm: The use of multicolor FISH to test various theories of nondisjunction
51. Interchromosomal effect in balanced translocations
52. Meiotic segregation, recombination and gamete aneuploidy assessed in a t(1:10) (p22.1;q22.3) reciprocal translocation carrier by three and four probe multicolor FISH in sperm
53. Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in-situ hybridization in infertile men