Literature DB >> 7315874

Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.

E J Breslau, C Disteche, J G Hall, H Thuline, P Cooper.   

Abstract

We analyzed the prometaphase chromosomes of 5 patients (including one pair of sibs) with the Brachmann-de Lange syndrome (BDLS), and did not find a significant chromosome abnormality in any of them. It appears that two distinct entities can be distinguished on clinical and chromosomal bases; the BDLS and the dup(3q) syndrome. We still recommend chromosome studies in any patients with BDLS and BDLS-like manifestations.

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Year:  1981        PMID: 7315874     DOI: 10.1002/ajmg.1320100211

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrences.

Authors:  K L Russell; J E Ming; K Patel; L Jukofsky; M Magnusson; I D Krantz
Journal:  Am J Med Genet       Date:  2001-12-15

Review 2.  Intrachromosomal insertions: a case report and a review.

Authors:  K Madan; F H Menko
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

3.  Reciprocal translocation 14q;21q in a patient with the Brachmann-de Lange syndrome.

Authors:  W G Wilson; J M Kennaugh; J P Kugler; H E Wyandt
Journal:  J Med Genet       Date:  1983-12       Impact factor: 6.318

  3 in total

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