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Literature DB >> 2339685

Genomic imprinting and the Beckwith-Wiedemann syndrome.

K W Brown, J C Williams, N J Maitland, M G Mott.

Abstract

Entities: Disease

Mesh：

Year: 1990 PMID： 2339685 PMCID： PMC1683593

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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12 in total

1. Maternal allele loss in Wilms' tumour.

Authors: J C Williams; K W Brown; M G Mott; N J Maitland
Journal: Lancet Date: 1989-02-04 Impact factor: 79.321

2. Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11.

Authors: J K Wales; V Walker; I E Moore; P T Clayton
Journal: Eur J Pediatr Date: 1986-04 Impact factor: 3.183

3. Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases.

Authors: H Journel; J Lucas; C Allaire; F Le Mée; G Defawe; M Lecornu; H Jouan; M Roussey; B Le Marec
Journal: Ann Genet Date: 1985

4. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

Authors: A Koufos; P Grundy; K Morgan; K A Aleck; T Hadro; B C Lampkin; A Kalbakji; W K Cavenee
Journal: Am J Hum Genet Date: 1989-05 Impact factor: 11.025

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. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.

Authors: A E Reeve; S A Sih; A M Raizis; A P Feinberg
Journal: Mol Cell Biol Date: 1989-04 Impact factor: 4.272

7. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome.

Authors: M Waziri; S R Patil; J W Hanson; J A Bartley
Journal: J Pediatr Date: 1983-06 Impact factor: 4.406

8. Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.

Authors: W T Schroeder; L Y Chao; D D Dao; L C Strong; S Pathak; V Riccardi; W H Lewis; G F Saunders
Journal: Am J Hum Genet Date: 1987-05 Impact factor: 11.025

9. 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

10. Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

Authors: C Turleau; J de Grouchy; F Chavin-Colin; H Martelli; M Voyer; R Charlas
Journal: Hum Genet Date: 1984 Impact factor: 4.132

10 in total

1. Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.

Authors: A Nyström; J E Cheetham; W Engström; P N Schofield
Journal: Eur J Pediatr Date: 1992-07 Impact factor: 3.183

2. Uses and limitations of twin studies.

Authors: S Bundey
Journal: J Neurol Date: 1991-10 Impact factor: 4.849

3. 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 4. Genomic imprinting: mechanism and role in human pathology.

Authors: B Tycko
Journal: Am J Pathol Date: 1994-03 Impact factor: 4.307

5. Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

Authors: N Tommerup; C A Brandt; S Pedersen; L Bolund; J Kamper
Journal: J Med Genet Date: 1993-11 Impact factor: 6.318