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Literature DB >> 1972981

PCR detection of two RFLP's at the D21S13 locus.

P Stinissen¹, A Vandenberghe, C Van Broeckhoven.

Abstract

Mesh：

Year: 1990 PMID： 1972981 PMCID： PMC331056 DOI： 10.1093/nar/18.12.3672

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

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2 in total

1. A high frequency EcoRI RFLP detected at the D21S13 locus.

Authors: P Stinissen; A Vandenberghe; C Van Broeckhoven
Journal: Nucleic Acids Res Date: 1990-03-11 Impact factor: 16.971

2. Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.

Authors: K Gardiner; M Horisberger; J Kraus; U Tantravahi; J Korenberg; V Rao; S Reddy; D Patterson
Journal: EMBO J Date: 1990-01 Impact factor: 11.598

2 in total

9 in total

1. 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

2. Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis.

Authors: V C Sheffield; J S Beck; B Nichols; A Cousineau; A C Lidral; E M Stone
Journal: Am J Hum Genet Date: 1992-03 Impact factor: 11.025

3. 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

PCR detection of two RFLP's at the D21S13 locus.

1. A high frequency EcoRI RFLP detected at the D21S13 locus.

2. Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.

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

2. Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis.

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

4. Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques.

5. PCR detection of the frequent TaqI RFLP at locus D21S13E.

6. New nucleotide sequence data on the EMBL File Server.

7. Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.

8. A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

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