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6 in total

Review 1. Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Authors: M P Hitchins; P Stanier; M A Preece; G E Moore
Journal: J Med Genet Date: 2001-12 Impact factor: 6.318

Review 2. The genetics of the Silver-Russell syndrome.

Authors: Michael A Preece
Journal: Rev Endocr Metab Disord Date: 2002-12 Impact factor: 6.514

3. [Child language development delay in craniofacial dysplasia].

Authors: C Schwemmle; K Lüerssen; R Tolloczko; M Ptok
Journal: HNO Date: 2004-02 Impact factor: 1.284

4. Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype.

Authors: Jet Bliek; Paulien Terhal; Marie-José van den Bogaard; Saskia Maas; Ben Hamel; Georgette Salieb-Beugelaar; Marleen Simon; Tom Letteboer; Jasper van der Smagt; Hester Kroes; Marcel Mannens
Journal: Am J Hum Genet Date: 2006-03-01 Impact factor: 11.025

5. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.

Authors: H Yoshihashi; K Maeyama; R Kosaki; T Ogata; M Tsukahara; Y Goto; J Hata; N Matsuo; R J Smith; K Kosaki
Journal: Am J Hum Genet Date: 2000-06-12 Impact factor: 11.025

Review 6. Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.

Authors: Katrin Õunap
Journal: Mol Syndromol Date: 2016-07-06

6 in total