Literature DB >> 4279289

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

B E Schuh, B R Korf, M J Salwen.   

Abstract

Mesh：

Year:  1974        PMID： 4279289      PMCID： PMC1013148          DOI： 10.1136/jmg.11.3.297

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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

Authors:  W Vogel
Journal:  Humangenetik       Date:  1972

4.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

5.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

6.  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

7.  [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

8.  [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].

Authors:  S Carpentier; M O Rethoré; J Lejeune
Journal:  Ann Genet       Date:  1972-12

9.  Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

Authors:  U Francke
Journal:  Am J Hum Genet       Date:  1972-03       Impact factor: 11.025

10.  [A case of G-G translocation in tandem].

Authors:  J Lejeune; R Berger; O R Vidal; M O Réthoré
Journal:  Ann Genet       Date:  1965
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  6 in total

1.  Fusion of two apparently intact human X chromosomes.

Authors:  A K Sinha; S Pathak; J J Nora
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

2.  Single Cd band in dicentric translocations with one suppressed centromere.

Authors:  A Daniel
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

3.  Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.

Authors:  A T Tharapel; R Redheendran; C B Mankinen; M K Kukolich
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

4.  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

5.  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

6.  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
  6 in total

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