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Literature DB >> 2395674

Dinucleotide repeat polymorphism located at D21S120.

M Burmelster¹, D R Cox, R M Myers.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 1990 PMID： 2395674 PMCID： PMC332044 DOI： 10.1093/nar/18.16.4969

Source DB: PubMed Journal: Nucleic Acids Res ISSN： 0305-1048 Impact factor: 16.971

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1 in total

1. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.

Authors: M Litt; J A Luty
Journal: Am J Hum Genet Date: 1989-03 Impact factor: 11.025

1 in total

13 in total

1. Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

Authors: M B Peterson; M Frantzen; S E Antonarakis; A C Warren; C Van Broeckhoven; A Chakravarti; T K Cox; C Lund; B Olsen; H Poulsen
Journal: Am J Hum Genet Date: 1992-09 Impact factor: 11.025

2. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.

Authors: B J Lorber; M Grantham; J Peters; H F Willard; T J Hassold
Journal: Am J Hum Genet Date: 1992-12 Impact factor: 11.025

3. DNA polymorphism analysis in families with recurrence of free trisomy 21.

Authors: C G Pangalos; C C Talbot; J G Lewis; P A Adelsberger; M B Petersen; J L Serre; M O Rethoré; M C de Blois; P Parent; A A Schinzel
Journal: Am J Hum Genet Date: 1992-11 Impact factor: 11.025

4. No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

Authors: A A Schinzel; P A Adelsberger; F Binkert; S Basaran; S E Antonarakis
Journal: Am J Hum Genet Date: 1992-02 Impact factor: 11.025

5. Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.

Authors: M B Petersen; J L Weber; S A Slaugenhaupt; A E Kwitek; M G McInnis; A Chakravarti; S E Antonarakis
Journal: Hum Genet Date: 1991-08 Impact factor: 4.132

Dinucleotide repeat polymorphism located at D21S120.

1. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.

1. Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

2. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.

3. DNA polymorphism analysis in families with recurrence of free trisomy 21.

4. No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

5. Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.

6. Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defects.

7. Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.

8. Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

9. Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.

10. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.