Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome
- 1 August 2002
- journal article
- letter
- Published by BMJ in Journal of Medical Genetics
- Vol. 39 (8), 575-581
- https://doi.org/10.1136/jmg.39.8.575
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Expression of mouse igf2 mRNA‐binding protein 3 and its implications for the developing central nervous systemJournal of Neuroscience Research, 2001
- Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndromeEuropean Journal of Human Genetics, 2001
- Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayJournal of Medical Genetics, 2000
- Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissuesEuropean Journal of Human Genetics, 1998
- Cloning of a gene highly overexpressed in cancer coding for a novel KH-domain containing proteinOncogene, 1997
- Maternal uniparental disomy 7 in Silver-Russell syndrome.Journal of Medical Genetics, 1997
- Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardationHuman Molecular Genetics, 1995
- Promoter-specific imprinting of the human insulin-like growth factor-II geneNature, 1994
- An infant with deletion of the distal long arm of chromosome 15 (q26.1→qter) and loss of insulin‐like growth factor 1 receptor geneAmerican Journal of Medical Genetics, 1991
- Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes.Journal of Medical Genetics, 1985