Literature DB >> 7129436

Prometaphase banding of human chromosomes with basic fuchsin.

J M Scheres, G F Merkx, T W Hustinx.   

Abstract

A technique is described for the production of detailed and richly contrasting G-band patterns in human prometaphase chromosomes with the aid of the triphenylmethane dye basic fuchsin. The usefulness of this method is illustrated by its application for the precise analysis of two chromosome 11 rearrangements. It is also demonstrated that high-resolution banding with basic fuchsin can reveal bands not present in the international standard idiogram of human prophase chromosomes (ISCN 1981). The technique described can also be used for easy recognition of the late replicating X chromosome, which stains darker than its early replicating homologue. A preliminary analysis of the late replicating X chromosomes in a 49,XXXXY individual suggests that the three supernumerary X chromosomes do not necessarily replicate synchronously.

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Year:  1982        PMID: 7129436     DOI: 10.1007/bf00291322

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


  11 in total

1.  High resolution of human chromosomes.

Authors:  J J Yunis
Journal:  Science       Date:  1976-03-26       Impact factor: 47.728

2.  R- and CT-banding of human chromosomes with basic fuchsin.

Authors:  J M Scheres
Journal:  Histochemistry       Date:  1977-06-24

3.  Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.

Authors:  J J Yunis; N K Ramsay
Journal:  J Pediatr       Date:  1980-06       Impact factor: 4.406

4.  "Reverse" differential staining of sister chromatids.

Authors:  J M Scheres; T W Hustinx; F J Rutten; G F Merkx
Journal:  Exp Cell Res       Date:  1977-10-15       Impact factor: 3.905

5.  Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.

Authors:  E H Zackai; B S Emanuel
Journal:  Am J Med Genet       Date:  1980

6.  Mid-prophase human chromosomes. The attainment of 2000 bands.

Authors:  J J Yunis
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  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

8.  Banding of human chromosomes with basic fuchsin.

Authors:  J M Scheres; G F Merkx
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

9.  Chromosomes and cancer: new nomenclature and future directions.

Authors:  J J Yunis
Journal:  Hum Pathol       Date:  1981-06       Impact factor: 3.466

10.  An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature.

Authors: 
Journal:  Cytogenet Cell Genet       Date:  1981
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  8 in total

1.  Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Authors:  K Mangelschots; B Van Roy; F Speleman; N Van Roy; J Gheuens; J Beuten; I Buntinx; M N Van Thienen; H Willekens; J Dumon
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

2.  Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.

Authors:  C J Van Der Burgt; G F Merkx; A H Janssen; J C Mulder; R F Suijkerbuijk; D F Smeets
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

Review 3.  Prenatal diagnosis of common genetic disorders.

Authors:  M D Crawfurd
Journal:  BMJ       Date:  1988 Aug 20-27

4.  Molecular study of chromosome 15 in 22 patients with Angelman syndrome.

Authors:  J Beuten; K Mangelschots; I Buntinx; P Coucke; O F Brouwer; R C Hennekam; C Van Broeckhoven; P J Willems
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132

5.  The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24.

Authors:  F Baas; H Bikker; A Geurts van Kessel; R Melsert; P L Pearson; J J de Vijlder; G J van Ommen
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  A de novo X;13 translocation with abnormal phenotype.

Authors:  S V Hodgson; J C Barber; A Dowie; V Dubowitz
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

7.  49,XXXXY: a distinct phenotype. Three new cases and review.

Authors:  J Peet; D D Weaver; G H Vance
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

8.  Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Authors:  G Van Camp; M N Van Thienen; I Handig; B Van Roy; V S Rao; A Milunsky; A P Read; C T Baldwin; L A Farrer; M Bonduelle
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

  8 in total

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