Satellite III sequences on 14p and their relevance to Robertsonian translocation formation

Chromosome Research

Volumn 9, Issue 3, 2001, Pages 235-242

  Bandyopadhyay, R ^a   Berend, S A ^a   Page, S L ^a   Choo, K H A ^a   Shaffer, L G ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Acrocentric chromosome; Fluorescence in situ hybridization; Non disjunction; Repetitive DNA; Robertsonian translocation; Satellite III DNA

Indexed keywords

REPETITIVE DNA; SATELLITE DNA;

ACROCENTRIC CHROMOSOME; ARTICLE; BIRTH DEFECT; CHROMOSOME 13Q; CHROMOSOME 14Q; CHROMOSOME 21Q; CHROMOSOME REARRANGEMENT; DISEASE PREDISPOSITION; FETUS WASTAGE; HUMAN; HUMAN CELL; MEIOSIS; MENTAL RETARDATION MALFORMATION SYNDROME; NONDISJUNCTION; PREVALENCE; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SOMATIC CELL GENETICS;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 21; DNA, SATELLITE; DOWN SYNDROME; GENE REARRANGEMENT; HUMANS; KARYOTYPING; PARENTS; TRANSLOCATION, GENETIC; TRISOMY;

CRICETINAE; ROBERTSONIA;

EID: 0035049692     PISSN: 09673849     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1016652621226     Document Type: Article

References (38)

1. Concerted evolution of multigene families
2. Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes
3. Identification and characterization of satellite III subfamilies to the acrocentric chromosomes
4. Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: Implications for recombination between nonhomologues and Robertsonian translocations
5. A homologous subfamily of satellite III DNA on human chromosomes 14 and 22
6. A chromosome 14-specific human satellite III DNA subfamily that shows variable presence on different chromosomes 14
7. New goals for the U.S. Human Genome Project 1998-2003
8. Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant
9. Amplification of satellite III DNA in an unusually large chromosome 14p+ variant
10. Identification of DNA sequences flanking the breakpoint of human t(14q21 q) Robertsonian translocations
11. The location of four human satellite DNAs on human chromosomes
12. Satellite DNA sequences in the human acrocentric chromosomes: Information from translocations and heteromorphisms
13. Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in-situ hybridization
14. Beta satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes
15. A cytogenetic survey of 14,069 newborn infants. Incidence of chromosome abnormalities
16. Molecular cytogenetic characterization of 17 rob(13ql4q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints
17. The origin of aneuploidy in humans
18. Trisomy in man
19. Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements
20. Mutation rates of structural chromosome rearrangements in man
21. Location of satellite and homogeneous DNA sequences on human chromosomes
22. A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: Further studies on Robertsonian translocations
23. Role of the nucleolus organizer in the etiology of Down Syndrome
24. Nucleolus-organizer in the causation of chromosome abnormalities
25. Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation
26. Nonhomologous Robertsonian translocations form predominantly during female meiosis
27. Possible non random selection of D group chromosomes involved in centric-fusion translocations
28. Molecular mechanisms for constitutional chromosomal rearrangements in humans
29. Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations
30. Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes
31. Assignment of human satellite 1 DNA as revealed by fluorescent in-situ hybridization with oligonucleotides
32. The non-random participation of human acrocentric chromosomes in Robertsonian translocation
33. Long-range analyses of the centromeric regions of human chromosomes 13, 14 and 21: Identification of a narrow domain containing two key centromeric DNA elements
34. NOR associations with heterochromatin
35. A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes
36. Human beta satellite DNA: Genomic organization and sequence definition of a class of highly repetitive tandem DNA
37. Assignment of autosomal dominant spinocerebeller ataxia (SCA1) centromeric to the HLA region on the short arm of the chromosome 6, using multilocus linkage analysis