Literature DB >> 8256806

The Williams syndrome: evidence for possible autosomal dominant inheritance.

L S Sadler1, L K Robinson, K R Verdaasdonk, R Gingell.   

Abstract

We recently evaluated a mother and son with the Williams syndrome. Documentation of the clinical phenotype in two generations of this family suggests that some cases of the Williams syndrome are autosomal dominantly inherited. Recognition of the heritable nature of the Williams syndrome should prompt careful clinical evaluation of other at-risk relatives in order to provide accurate recurrence risk counseling.

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Year:  1993        PMID: 8256806     DOI: 10.1002/ajmg.1320470406

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


  21 in total

1.  Williams syndrome: an update on clinical and molecular aspects.

Authors:  K Metcalfe
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

2.  Late onset cerebellar metastasis from oesophageal adenocarcinoma in Williams Syndrome.

Authors:  Nicola Montano; Pasquale De Bonis; Libero Lauriola; Fabio Papacci; Corrado Lucantoni; Cesare Colosimo; Beatrice Cioni; Mario Meglio
Journal:  J Neurooncol       Date:  2008-04-08       Impact factor: 4.130

3.  Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.

Authors:  L R Osborne; S Soder; X M Shi; B Pober; T Costa; S W Scherer; L C Tsui
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

Review 4.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

5.  No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control.

Authors:  Judith Frohnauer; Almuth Caliebe; Stefan Gesk; Carl-Joachim Partsch; Reiner Siebert; Rainer Pankau; Jutta Jenderny
Journal:  Mol Cytogenet       Date:  2010-11-05       Impact factor: 2.009

6.  Genetic counseling of adults with Williams syndrome: a first study.

Authors:  Katrina Farwig; Amanda G Harmon; Kristina M Fontana; Carolyn B Mervis; Colleen A Morris
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

7.  Introduction: Williams syndrome.

Authors:  Colleen A Morris
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

8.  Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome.

Authors:  Holly H Hobart; Colleen A Morris; Carolyn B Mervis; Ariel M Pani; Doris J Kistler; Cecilia M Rios; Kendra W Kimberley; Ronald G Gregg; Patricia Bray-Ward
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

9.  Sudden unexpected death in a toddler with Williams syndrome.

Authors:  Henry F Krous; Carter Wahl; Amy E Chadwick
Journal:  Forensic Sci Med Pathol       Date:  2008-04-04       Impact factor: 2.007

10.  Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Authors:  A Mari; F Amati; R Mingarelli; A Giannotti; G Sebastio; V Colloridi; G Novelli; B Dallapiccola
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

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