Literature DB >> 8230171

Chromosome abnormalities and Williams-Beuren syndrome.

A Gosch, R Pankau.   

Abstract

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Year:  1993        PMID： 8230171      PMCID： PMC1016583          DOI： 10.1136/jmg.30.10.886

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


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  4 in total

1.  Familial Williams syndrome.

Authors:  X Cortada; K Taysi; A F Hartmann
Journal:  Clin Genet       Date:  1980-09       Impact factor: 4.438

2.  The Williams syndrome: objective definition and diagnosis.

Authors:  M Preus
Journal:  Clin Genet       Date:  1984-05       Impact factor: 4.438

3.  Differential diagnosis of the Williams and the Noonan syndromes.

Authors:  M Preus
Journal:  Clin Genet       Date:  1984-05       Impact factor: 4.438

4.  De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome.

Authors:  L Telvi; J M Pinard; R Ion; P M Sinet; A Nicole; J Feingold; O Dulac; A Pompidou; G Ponsot
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318
  4 in total

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