Literature DB >> 7372336

A deleted extra chromosome 22 identified by DNA replication banding.

M Parslow, J J Hoo, M Garry, F Rose.   

Abstract

The identification of a deleted extra chromosome 22 by means of the DNA replication banding pattern is reported. The characteristics of DNA replication banding, its advantages and superiority in chromosome identification are described.

Mesh：

Year:  1980        PMID： 7372336     DOI： 10.1007/bf00287050

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  5 in total

1.  Human Q and C chromosomal variations: distribution and incidence.

Authors:  W H McKenzie; H A Lubs
Journal:  Cytogenet Cell Genet       Date:  1975

2.  Combination of differential sister chromatid staining, G-banding pattern, and X-inactivation pattern.

Authors:  J J Hoo; M I Parslow; D Chambers
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

3.  An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.

Authors:  S E Bloom; C Goodpasture
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

4.  Analysis of DNA replication patterns of human fibroblast chromosomes: the replication map.

Authors:  P M Kondra; M Ray
Journal:  Hum Genet       Date:  1978-08-31       Impact factor: 4.132

5.  Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining.

Authors:  K H Grzeschik; M A Kim; R Johannsmann
Journal:  Humangenetik       Date:  1975-08-29
  5 in total
  4 in total

1.  Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Authors:  D H Lockwood; A Farrier; F Hecht; J Allanson
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

2.  The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families.

Authors:  L Iselius; J Lindsten; A Aurias; M Fraccaro; C Bastard; A M Bottelli; T H Bui; D Caufin; L Dalprà; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Authors:  A Schinzel; W Schmid; P Auf der Maur; H Moser; K H Degenhardt; M Geisler; A Grubisic
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  The 11q;22q translocation: a European collaborative analysis of 43 cases.

Authors:  M Fraccaro; J Lindsten; C E Ford; L Iselius
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132
  4 in total

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