Literature DB >> 5092710

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

M L Motl, J M Opitz.   

Abstract

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Year:  1971        PMID： 5092710     DOI： 10.1159/000152379

Source DB:  PubMed          Journal:  Hum Hered        ISSN： 0001-5652            Impact factor:   0.444


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  4 in total

1.  The de Lange syndrome in one of twins.

Authors:  G Carakushannsky; C Berthier
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

2.  Brachmann-de Lange syndrome in sibs.

Authors:  K K Naguib; A S Teebi; S A Al-Awadi; M J Marafie
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

3.  Discordance for Cornelia de Lange syndrome in twins.

Authors:  R E Stevenson; C I Scott
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

Review 4.  Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements.

Authors:  Cheryl DeScipio; Maninder Kaur; Dinah Yaeger; Jeffrey W Innis; Nancy B Spinner; Laird G Jackson; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2005-09-01       Impact factor: 2.802
  4 in total

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