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25. (Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation? Schönherr N; Meyer E; Eggermann K; Ranke MB; Wollmann HA; Eggermann T Eur J Med Genet; 2006; 49(5):414-8. PubMed ID: 16603426 [TBL] [Abstract][Full Text] [Related]
27. Is maternal duplication of 11p15 associated with Silver-Russell syndrome? Eggermann T; Meyer E; Obermann C; Heil I; Schüler H; Ranke MB; Eggermann K; Wollmann HA J Med Genet; 2005 May; 42(5):e26. PubMed ID: 15863658 [TBL] [Abstract][Full Text] [Related]
28. Epigenetics in Silver-Russell syndrome. Rossignol S; Netchine I; Le Bouc Y; Gicquel C Best Pract Res Clin Endocrinol Metab; 2008 Jun; 22(3):403-14. PubMed ID: 18538282 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. An unusual chromosome rearrangement in a patient with features of the Wolf-Hirschhorn syndrome. Williams MS; Josephson KD; Wargowski DS; Dewald GW WMJ; 1998 Apr; 97(4):42-5. PubMed ID: 9584686 [No Abstract] [Full Text] [Related]
32. Fetal akinesia sequence caused by nemaline myopathy. Lammens M; Moerman P; Fryns JP; Lemmens F; van de Kamp GM; Goemans N; Dom R Neuropediatrics; 1997 Apr; 28(2):116-9. PubMed ID: 9208412 [TBL] [Abstract][Full Text] [Related]
33. Silver-Russell syndrome as a cause for early intrauterine growth restriction. Falkert A; Dittmann K; Seelbach-Göbel B Prenat Diagn; 2005 Jun; 25(6):497-501. PubMed ID: 15966045 [TBL] [Abstract][Full Text] [Related]
34. Multiple abnormalities in a preterm infant with growth retardation. Cowett RM; Singer DB R I Med J (1976); 1984 May; 67(5):233-7. PubMed ID: 6588444 [No Abstract] [Full Text] [Related]
35. [Child language development delay in craniofacial dysplasia]. Schwemmle C; Lüerssen K; Tolloczko R; Ptok M HNO; 2004 Feb; 52(2):150-2. PubMed ID: 14968319 [No Abstract] [Full Text] [Related]
37. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)]. Le Chevalier C; Chabrolle JP; Rossier A Ann Pediatr (Paris); 1978 Nov; 25(9):501-4, 507. PubMed ID: 16114368 [No Abstract] [Full Text] [Related]
38. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin. López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814 [TBL] [Abstract][Full Text] [Related]
39. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22. de Beaufort C; Schneider F; Chafai R; Colette JM; Delneste D; Pierquin G Genet Couns; 2000; 11(2):181-2. PubMed ID: 10893671 [No Abstract] [Full Text] [Related]
40. [A 10-year survey on birth defects after in vitro fertilization-embryo transfer in Shanghai]. Han JL; Chen H; Niu ZH; Sun YJ; Sun XX; Zhao XM; Kuang YP; Teng XM; Ji YZ; Wang YB; Feng Y Zhonghua Fu Chan Ke Za Zhi; 2010 Feb; 45(2):124-7. PubMed ID: 20420783 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]