+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Molecular fine structure of the centromeric region of chromosome 21 analysis of nondisjunction events yielding down syndrome



Molecular fine structure of the centromeric region of chromosome 21 analysis of nondisjunction events yielding down syndrome



American Journal of Human Genetics 39(3 Suppl.): A222




Please choose payment method:






(PDF emailed within 1 workday: $29.90)

Accession: 028734998

Download citation: RISBibTeXText


Related references

The centromeric region of chromosome 21 molecular and clinical studies of nondisjunction. Pediatric Research 20(4 Part 2): 267A, 1986

Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome. Chromosoma (Berlin) 107(3): 166-172, 1998

Composition and structure of the centromeric region of rice chromosome 8. Plant Cell 16(4): 967-976, 2004

Composition and Structure of the Centromeric Region of Rice Chromosome 8. The Plant Cell 16(4): 967-976, 2004

Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction. American Journal of Medical Genetics. Suppl. 7: 162-168, 1990

Structure of repeated sequences in the centromeric region of the human Y chromosome. Development 101 Suppl: 93, 1987

Analysis of the centromeric region of chromosome 21. Cytogenetics & Cell Genetics 77(Suppl. 1): 15, 1997

Fine structure analysis at the 2D3-2F5 region of the X-chromosome of Drosophila melanogaster. Genetika 11 (1) 73-79, 1975

Folate deficiency and the molecular determinants of chromosome instability - possible link to meiotic nondisjunction and down syndrome. Folate and human development: 43-70, 2002

The TX; Y test for the detection of nondisjunction and chromosome breakage in Drosophila melanogaster. I. Analysis of spontaneous events and results of male exposure. Mutation Research 203(6): 427-444, 1988

Molecular characterization of the Alagille syndrome chromosome region and physical mapping of chromosome 20p by PFGE-analysis. American Journal of Human Genetics 51(4 Suppl. ): A246, 1992

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21. American Journal of Human Genetics 42(2): 227-236, 1988

Molecular genetic variation in the centromeric region of the X chromosome in three Drosophila ananassae populations. II. The Om(1D) locus. Molecular Biology and Evolution 6(6): 624-635, 1989

Use of a chromosome 21 cloned dna probe for the analysis of nondisjunction in downs syndrome. Human Genetics 66(1): 54-56, 1984

Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome. Human Genetics 81(2): 113-119, 1989