Literature DB >> 6517059

A male-specific DNA probe detects heterochromatin sequences in a familial Yq- chromosome.

Y F Lau, S Schonberg.   

Abstract

Using a recombinant DNA probe, we have demonstrated the presence of residual 3.4-kilobase (kb) repeat sequences in a family with a Yq- chromosome. The heterochromatin of this Y variant was not readily detectable with conventional chromosome-banding techniques. These data suggest that the breakpoint of the deletion occurs at the heterochromatin region proximal to the euchromatin/heterochromatin junction.

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Year:  1984        PMID： 6517059      PMCID： PMC1684645     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


  4 in total

1.  A rapid screening test for antenatal sex determination.

Authors:  Y F Lau; J C Huang; A M Dozy; Y W Kan
Journal:  Lancet       Date:  1984-01-07       Impact factor: 79.321

2.  Repeated sequence specific to human males.

Authors:  H Cooke
Journal:  Nature       Date:  1976-07-15       Impact factor: 49.962

3.  Localisation of a male-specific DNA fragment to a sub-region of the human Y chromosome.

Authors:  C J Bostock; J R Gosden; A R Mitchell
Journal:  Nature       Date:  1978-03-23       Impact factor: 49.962

4.  Regional assignment of a 2.1-kb repetitive sequence to the distal part of the human Y heterochromatin.

Authors:  J Schmidtke; M Schmid
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132
  4 in total
  8 in total

1.  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

2.  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

3.  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

4.  Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization.

Authors:  B Trask; G van den Engh; D Pinkel; J Mullikin; F Waldman; H van Dekken; J Gray
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

5.  An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA content.

Authors:  M Witt; K Michalczak; A Latos-Bielenska; J Jaruzelska; I Kuczora; M Lopez
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

6.  Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

Authors:  D Pinkel; T Straume; J W Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

7.  Quantitative analysis of sex-chromosome mosaicism with X-Y DNA probes.

Authors:  C M Disteche; H Saal; C Friedman; V Sybert; H Thuline
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

Review 8.  The Role of Number of Copies, Structure, Behavior and Copy Number Variations (CNV) of the Y Chromosome in Male Infertility.

Authors:  Fabrizio Signore; Caterina Gulìa; Raffaella Votino; Vincenzo De Leo; Simona Zaami; Lorenza Putignani; Silvia Gigli; Edoardo Santini; Luca Bertacca; Alessandro Porrello; Roberto Piergentili
Journal:  Genes (Basel)       Date:  2019-12-29       Impact factor: 4.096
  8 in total

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