Literature DB >> 955629

The trisomy 18 syndrome with an E/G translocation.

D Dziekanowska, P Dziuba, T Sobański.   

Abstract

An infant with a typical Edwards syndrome and a modal chromosome number of 46 is reported. In all cells analyzed one chromosome G was missing and an additional chromosome similar to a pair No. 16 was present. The phenotype of the child indicates that the extra element is a translocation between G and 18 chromosomes as in one case described previously.

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Year:  1976        PMID： 955629     DOI： 10.1007/BF00270865

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


  5 in total

1.  A NEW TRISOMY-TRANSLOCATION CHROMOSOME (LONG-ARM E/E).

Authors:  R A ROHDE; A LEE; S SAPIN
Journal:  Lancet       Date:  1963-12-21       Impact factor: 79.321

2.  [Partial trisomy 18 caused by insertion or translocation 4/18].

Authors:  F GAGNON; L ARCHAMBAULT; E LABERGE; N KATYK-LONGTIN
Journal:  Union Med Can       Date:  1963-03

3.  The E syndrome (trisomy 17-18) resulting from a maternal chromosomal translocation.

Authors:  H R BRODIE; L DALLAIRE
Journal:  Can Med Assoc J       Date:  1962-09-08       Impact factor: 8.262

4.  Trisomy 18 with an E-G translocation (46,XY,21-t(21q18q)+). Identification of the component chromosomes by several laboratory techniques.

Authors:  M M Cohen; A B Finch; H A Lubs
Journal:  Ann Genet       Date:  1972-03

5.  Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.

Authors:  B Eriksson; M Fraccaro; M Hultén; J Lindsten; C Thorén; L Tiepolo
Journal:  Ann Genet       Date:  1971-12
  5 in total
  1 in total

1.  Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).

Authors:  M Niazi; D V Coleman; P Saldaña-Garcia
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318
  1 in total

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