Literature DB >> 1034016

The de Lange syndrome in one of twins.

G Carakushannsky, C Berthier.   

Abstract

A pair of female monozygotic twins, one of them affected by the de Lange syndrome is described for the first time. Monozygosity was established by most of the accepted standards in use at the present time. Speculation is offered as to whether the discordance in the manifestation of the syndrome provides any clues for understanding its controversial pathogenesis. In this regard two genetic mechanisms are discussed. One is the hypothesis of a chromosomal or mitotic instability. The other possibility would be a postzygotic new mutation of a gene or large effect.

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Year:  1976        PMID: 1034016      PMCID: PMC1013450          DOI: 10.1136/jmg.13.5.404

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


  3 in total

1.  Chromosomes in the de Lange syndrome.

Authors:  S Sachdeva; G F Smith
Journal:  Lancet       Date:  1973-04-14       Impact factor: 79.321

2.  Studies of malformation syndromes XXVA. Phenotypic and genetic studies of the Brachmann-de Lange Syndrome.

Authors:  M L Motl; J M Opitz
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

3.  [Cornelia de Lange syndrome I in twins (Amsterdam type of degeneration)].

Authors:  H Kroth
Journal:  Arch Kinderheilkd       Date:  1966-02
  3 in total

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