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4. Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. Hitchins MP; Monk D; Bell GM; Ali Z; Preece MA; Stanier P; Moore GE Eur J Hum Genet; 2001 Feb; 9(2):82-90. PubMed ID: 11313740 [TBL] [Abstract][Full Text] [Related]
5. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Joyce CA; Sharp A; Walker JM; Bullman H; Temple IK Hum Genet; 1999 Sep; 105(3):273-80. PubMed ID: 10987657 [TBL] [Abstract][Full Text] [Related]
6. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome. Monk D; Wakeling EL; Proud V; Hitchins M; Abu-Amero SN; Stanier P; Preece MA; Moore GE Am J Hum Genet; 2000 Jan; 66(1):36-46. PubMed ID: 10631135 [TBL] [Abstract][Full Text] [Related]
7. Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions. Hitchins MP; Stanier P; Preece MA; Moore GE J Med Genet; 2001 Dec; 38(12):810-9. PubMed ID: 11748303 [TBL] [Abstract][Full Text] [Related]
8. Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays. Kim Y; Kim SS; Kim G; Park S; Park IS; Yoo HW Clin Genet; 2005 Mar; 67(3):267-9. PubMed ID: 15691366 [No Abstract] [Full Text] [Related]
9. Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10. Eggermann T; Begemann M; Gogiel M; Palomares M; Vallespín E; Fernández L; Cazorla R; Spengler S; García-Miñaúr S Am J Med Genet A; 2012 Nov; 158A(11):2815-9. PubMed ID: 22987336 [TBL] [Abstract][Full Text] [Related]
10. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome. Yoshihashi H; Maeyama K; Kosaki R; Ogata T; Tsukahara M; Goto Y; Hata J; Matsuo N; Smith RJ; Kosaki K Am J Hum Genet; 2000 Aug; 67(2):476-82. PubMed ID: 10856193 [TBL] [Abstract][Full Text] [Related]
11. Silver-Russell syndrome and ring chromosome 7. Wakeling EL; Hitchins M; Stanier P; Monk D; Moore GE; Preece MA J Med Genet; 2000 May; 37(5):380. PubMed ID: 10905891 [No Abstract] [Full Text] [Related]
12. Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases. Bernard LE; Peñaherrera MS; Van Allen MI; Wang MS; Yong SL; Gareis F; Langlois S; Robinson WP Am J Med Genet; 1999 Nov; 87(3):230-6. PubMed ID: 10564876 [TBL] [Abstract][Full Text] [Related]
13. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis. Monk D; Smith R; Arnaud P; Preece MA; Stanier P; Beechey CV; Peters J; Kelsey G; Moore GE Mamm Genome; 2003 Dec; 14(12):805-16. PubMed ID: 14724735 [TBL] [Abstract][Full Text] [Related]
14. Evidence against GRB10 as the gene responsible for Silver-Russell syndrome. McCann JA; Zheng H; Islam A; Goodyer CG; Polychronakos C Biochem Biophys Res Commun; 2001 Sep; 286(5):943-8. PubMed ID: 11527390 [TBL] [Abstract][Full Text] [Related]
15. What is the evidence for causal epigenetic influences on the Silver-Russell syndrome phenotype? Moore GE Epigenomics; 2011 Oct; 3(5):529-31. PubMed ID: 22126241 [No Abstract] [Full Text] [Related]
16. Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome. Monk D; Bentley L; Beechey C; Hitchins M; Peters J; Preece MA; Stanier P; Moore GE J Med Genet; 2002 Aug; 39(8):575-81. PubMed ID: 12161597 [No Abstract] [Full Text] [Related]
17. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands. Preece MA; Abu-Amero SN; Ali Z; Abu-Amero KK; Wakeling EL; Stanier P; Moore GE J Med Genet; 1999 Jun; 36(6):457-60. PubMed ID: 10874633 [TBL] [Abstract][Full Text] [Related]
18. Silver-Russell syndrome and exclusion of uniparental disomy. Ayala-Madrigal ML; Shaffer LG; Ramírez-Dueñas ML Clin Genet; 1996 Dec; 50(6):494-7. PubMed ID: 9147881 [TBL] [Abstract][Full Text] [Related]
19. Quantification of GRB10 in 7p12-p14 by fluorogenic 5' nuclease chemistry and application for genetic diagnosis in Silver-Russell syndrome. Eggermann T; Meyer E; Wollmann HA Ann Genet; 2004; 47(1):99-102. PubMed ID: 15050880 [No Abstract] [Full Text] [Related]