Literature DB >> 2994545

Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy.

C Turleau, J de Grouchy.   

Abstract

Thirteen previously unreported patients with Beckwith-Wiedemann syndrome are reported. They include two unrelated patients having developed nephroblastoma, and three sibs. High resolution banding techniques failed to show any evidence of trisomy 11p15 in any of these 13 patients. The clinical pictures of Beckwith-Wiedemann syndrome with and without trisomy 11p15 are compared.

Entities:  

Mesh：

Year:  1985        PMID： 2994545

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  12 in total

1.  Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Authors:  C Moutou; C Junien; I Henry; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

Review 2.  Wiedemann-Beckwith syndrome.

Authors:  W Engström; S Lindham; P Schofield
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

3.  Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.

Authors:  J Eggenschwiler; T Ludwig; P Fisher; P A Leighton; S M Tilghman; A Efstratiadis
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

Review 4.  Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.

Authors:  A Slavotinek; L Gaunt; D Donnai
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

5.  Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.

Authors:  M Mannens; R M Slater; C Heyting; J Bliek; J de Kraker; N Coad; P de Pagter-Holthuizen; P L Pearson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

6.  Uniparental disomy occurs infrequently in Wilms tumor patients.

Authors:  P Grundy; B Wilson; P Telzerow; W Zhou; M C Paterson
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

7.  Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.

Authors:  P Couillin; M Azoulay; I Henry; N Ravisé; M C Grisard; C Jeanpierre; F Barichard; P Metezeau; J J Candelier; W Lewis
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

8.  Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.

Authors:  I Henry; M Jeanpierre; P Couillin; F Barichard; J L Serre; H Journel; A Lamouroux; C Turleau; J de Grouchy; C Junien
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

9.  Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

Authors:  M H Little; D B Thomson; N K Hayward; P J Smith
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

10.  Beckwith-wiedemann syndrome and neural crest tumors. A report of two cases.

Authors:  D Sirinelli; B Silberman; J J Baudon; P Sinnassamy; M Gruner; J P Montagne
Journal:  Pediatr Radiol       Date:  1989
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