Literature DB >> 648195

The identification of a repeated DNA sequence involved in the karyotype polymorphism of the human Y chromosome.

R D McKay, M Bobrow, H J Cooke.   

Abstract

We show that individual men are polymorphic for the amount of two different repeated DNA sequences. The amount of one of these sequences is proportional to the length of the brightly fluorescent heterochromatin on the Y chromosome. There are no detectable alterations in sequence between polymorphic individuals. Female DNA contains sequences complementary to those found on the Y, but at a much reduced level.

Entities:  

Mesh：

Substances：

Year:  1978        PMID： 648195     DOI： 10.1159/000130875

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  29 in total

1.  Sex determination and species exclusion in forensic samples with probe cY97.

Authors:  P Fattorini; S Cacció; S Gustincich; J Wolfe; B M Altamura; G Graziosi
Journal:  Int J Legal Med       Date:  1991       Impact factor: 2.686

Review 2.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

3.  A rapid method for detection of Y-chromosomal DNA from dried blood specimens by the polymerase chain reaction.

Authors:  M Witt; R P Erickson
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

4.  An improved method for detecting Y chromosomal DNA.

Authors:  J R Stalvey; R P Erickson
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

5.  Identification of a case of Y:18 translocation using a Y-specific repetitive DNA probe.

Authors:  Y F Lau; K L Ying; G N Donnell
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping.

Authors:  B Trask; G van den Engh; B Mayall; J W Gray
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

7.  18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence.

Authors:  S G Vorsanova; Y B Yurov; I A Alexandrov; I A Demidova; S P Mitkevich; A F Tirskaia
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

8.  A Y/5 translocation in a 45,X male with cri du chat syndrome.

Authors:  B Weber; W Schempp; U Orth; H Seidel; A Gal
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

Review 9.  Satellite DNA and heterochromatin variants: the case for unequal mitotic crossing over.

Authors:  D M Kurnit
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

10.  Characterization of an unusually conserved AluI highly reiterated DNA sequence family from the honeybee, Apis mellifera.

Authors:  S Tarès; J M Cornuet; P Abad
Journal:  Genetics       Date:  1993-08       Impact factor: 4.562
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.