Literature DB >> 12424439

The genetics of the Silver-Russell syndrome.

Michael A Preece1.   

Abstract

Mesh：

Year:  2002        PMID： 12424439     DOI： 10.1023/a:1020961909991

Source DB:  PubMed          Journal:  Rev Endocr Metab Disord        ISSN： 1389-9155            Impact factor:   6.514


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  85 in total

1.  Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

Authors:  T Eggermann; H A Wollmann; R Kuner; K Eggermann; H Enders; P Kaiser; M B Ranke
Journal:  Hum Genet       Date:  1997-09       Impact factor: 4.132

2.  Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.

Authors:  P K Rogan; J R Seip; D J Driscoll; P R Papenhausen; V P Johnson; S Raskin; A L Woodward; M G Butler
Journal:  Am J Med Genet       Date:  1996-03-01

3.  Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely.

Authors:  K Eggermann; H A Wollmann; G Binder; P Kaiser; M B Ranke; T Eggermann
Journal:  Ann Genet       Date:  1999

4.  Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)

Authors:  M L Ramírez-Dueñas; C Medina; R Ocampo-Campos; H Rivera
Journal:  Clin Genet       Date:  1992-01       Impact factor: 4.438

5.  Human PEG1/MEST, an imprinted gene on chromosome 7.

Authors:  S Kobayashi; T Kohda; N Miyoshi; Y Kuroiwa; K Aisaka; O Tsutsumi; T Kaneko-Ishino; F Ishino
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

6.  Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines.

Authors:  G Piras; A El Kharroubi; S Kozlov; D Escalante-Alcalde; L Hernandez; N G Copeland; D J Gilbert; N A Jenkins; C L Stewart
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

7.  Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.

Authors:  E L Wakeling; S N Abu-Amero; P Stanier; M A Preece; G E Moore
Journal:  Eur J Hum Genet       Date:  1998 Mar-Apr       Impact factor: 4.246

8.  Evidence against a major role of PEG1/MEST in Silver-Russell syndrome.

Authors:  A M Riesewijk; N Blagitko; A A Schinzel; L Hu; U Schulz; B C Hamel; H H Ropers; V M Kalscheuer
Journal:  Eur J Hum Genet       Date:  1998 Mar-Apr       Impact factor: 4.246

9.  An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features.

Authors:  A A Schinzel; W P Robinson; F Binkert; A Fanconi
Journal:  Clin Dysmorphol       Date:  1994-01       Impact factor: 0.816

10.  Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.

Authors:  D Kotzot; S Schmitt; F Bernasconi; W P Robinson; I W Lurie; H Ilyina; K Méhes; B C Hamel; B J Otten; M Hergersberg
Journal:  Hum Mol Genet       Date:  1995-04       Impact factor: 6.150
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