Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?
Open Access
- 5 May 2011
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 155 (6), 1236-1245
- https://doi.org/10.1002/ajmg.a.34009
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Russell–Silver syndromeAmerican Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2010
- The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1American Journal of Human Genetics, 2009
- Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree ofH19Hypomethylation Associates with Phenotype Severity and Genital and Skeletal AnomaliesJournal of Clinical Endocrinology & Metabolism, 2009
- Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypesJournal of Medical Genetics, 2008
- The genetic aetiology of Silver-Russell syndromeJournal of Medical Genetics, 2007
- Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regionsJournal of Medical Genetics, 2001
- 3M dwarfism: a study of two further sibs.Journal of Medical Genetics, 1989
- 3-M syndromeAmerican Journal of Medical Genetics, 1989
- Further delineation of the 3‐M syndrome with review of the literatureAmerican Journal of Medical Genetics, 1987
- 3-M Slender-Boned NanismAmerican Journal of Diseases of Children, 1981