Literature DB >> 573239

G-banding patterns of high-resolution human chromosomes 6--22, X, and Y.

J J Yunis, D W Ball, J R Sawyer.   

Abstract

A precise schematic representation of the number, height, position, and staining intensity of the Giemsa bands of late prophase, prometaphase, early metaphase, and mid-metaphase chromosomes 6--22, X, and Y is presented. Late prophase chromosomes were found to have 2--2 1/2 times the length and 3--3 1/2 times the number of bands previously observed in mid-metaphase, whereas prometaphases and early metaphases were intermediate in length and number of bands. In this work, the maximum number of bands observed per haploid set in late prophase was 1353, while more than 350 were generally found in mid-metaphase.

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Year:  1979        PMID: 573239     DOI: 10.1007/bf00569349

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


  2 in total

1.  Characterization of banding patterns of metaphase-prophase G-banded chromosomes and their use in gene mapping.

Authors:  J J Yunis; J R Sawyer; D W Ball
Journal:  Cytogenet Cell Genet       Date:  1978

2.  The characterization of high-resolution G-banded chromosomes of man.

Authors:  J J Yunis; J R Sawyer; D W Ball
Journal:  Chromosoma       Date:  1978-08-14       Impact factor: 4.316

  2 in total
  21 in total

1.  On the structure and polymorphism of the human chromosome no. 15.

Authors:  F Wachtler; R Musil
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

2.  A pachytene chromomere map of chromosome 10.

Authors:  D A Hungerford; A M Hungerford
Journal:  Hum Genet       Date:  1979-11       Impact factor: 4.132

3.  High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19.

Authors:  J R Sawyer; R A Rowe; S J Hassed; C Cunniff
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

4.  Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.

Authors:  U Trautmann; R A Pfeiffer; U Seufert-Satomi; H U Tietze
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

5.  Complete pachytene chromomere karyotypes of human spermatocyte bivalents.

Authors:  J M Luciani; M R Guichaoua; M R Morazzani
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Prenatal detection of an unstable ring 21 chromosome.

Authors:  G Stetten; B Sroka; V L Corson; C D Boehm
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Terminal rearrangement of chromosomes 21 detected in amniotic fluid, resulting in a trisomy 21.

Authors:  G Cohen; A Manuel; M Cohen; S Endrey-Walder; W McBride
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  A deletion of heterochromatin only of the Y chromosome in an azoospermic male.

Authors:  G Cohen; A Manuel; M Cohen; K Fagan; H Grunstein
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.

Authors:  M Zatz; A M Vianna-Morgante; P Campos; A J Diament
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

10.  Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Authors:  V R Babu; D L Van Dyke; C E Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

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