Literature DB >> 4115277

Identification of G-group chromosomes involved in a G-G tandem-translocation by the giemsa-band technique.

W Vogel.   

Abstract

Mesh：

Year:  1972        PMID： 4115277     DOI： 10.1007/bf00278046

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  6 in total

1.  Pericentric inversion in a family with a 21/22 translocation.

Authors:  D Soudek; R Laxová; R Adámek
Journal:  Cytogenetics       Date:  1968

2.  Down's syndrome associated with a familial (21q-; 22q+) translocation.

Authors:  M M Cohen; R G Davidson
Journal:  Cytogenetics       Date:  1967

3.  Analysis of the human karyotype using a reassociation technique.

Authors:  W Schnedl
Journal:  Chromosoma       Date:  1971       Impact factor: 4.316

4.  Fluorescent chromosomes of a tandem translocation in a mongol patient.

Authors:  S Sachdeva; J Wodnicki; G F Smith
Journal:  J Ment Defic Res       Date:  1971-09

5.  [Tandem chromosome (G-G) with satellites on short and long arm in a patient with trisomy G1].

Authors:  W Vogel; H Reinwein; W Engel
Journal:  Humangenetik       Date:  1970

6.  A simplified method of demonstrating Giemsa-band pattern in human chromosomes.

Authors:  J P Chaudhuri; W Vogel; I Voiculescu; U Wolf
Journal:  Humangenetik       Date:  1971
  6 in total
  11 in total

1.  [Comparison of the structure of chromatids of Homo sapiens and Pan troglodytes (author's transl)].

Authors:  J Lejeune; B Dutrillaux; M O Rethoré; M Prieur
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

2.  [Two subterminal heterochromatin regions in a rare form of 21-21 translocation].

Authors:  M Bartsch-Sandhoff; H Schade
Journal:  Humangenetik       Date:  1973

3.  A 21-21 tandem translocation with satellites on both long and short arms.

Authors:  B E Schuh; B R Korf; M J Salwen
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

4.  Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1974-01-22

5.  Down's syndrome with a recombinant tandem duplication of chromosome 21 derived from a maternal ring.

Authors:  R T Howell; A McDermott; A Gardner; V Dickinson
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

6.  A case of Down's syndrome resulting from mirror duplication of chromosome 21.

Authors:  C Stoll; A Pennerath; C Lausecker
Journal:  Eur J Pediatr       Date:  1982-02       Impact factor: 3.183

7.  Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin.

Authors:  R A Pfeiffer; J Loidl
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors:  J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

9.  No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Authors:  C Pangalos; D Théophile; P M Sinet; A Marks; D Stamboulieh-Abazis; Z Chettouh; M Prieur; C Verellen; M O Rethoré; J Lejeune
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

10.  Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.

Authors:  A Hagemeijer; E M Smit
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132
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