S Rossignol, V Steunou, C Chalas, A Kerjean, … - British Medical Journal, 2006 - jmg.bmj.com Online First articles must include the digital object identifier (DOIs) and date
of initial publication. establish publication priority; they are indexed by
PubMed from initial publication. Citations to may be posted when available ... Cited by 5 - Related articles
S Rossignol, V Steunou, C Chalas, A Kerjean, … - British Medical Journal, 2006 - jmg.bmj.com Background: Genomic imprinting refers to an epigenetic marking resulting in
monoallelic gene expression and has a critical role in fetal development.
Various imprinting diseases have recently been reported in humans and ... Cited by 24 - Related articles - BL Direct - All 4 versions
- ►endojournals.org [PDF] B Heude, KK Ong, R Luben, NJ Wareham, … - Journal of Clinical Endocrinology & Metabolism, 2007 - Endocrine Soc Page 1. 1 Study of association between common variation in the IGF2 gene and
indices of obesity and body size in middle-age men and women. ... Cited by 1 - Related articles - All 2 versions
- ►endojournals.org [PDF] I Netchine, S Rossignol, MN Dufourg, S Azzi, … - Journal of Clinical Endocrinology & Metabolism, 2007 - Endocrine Soc 11p15 ICR1 loss of methylation is a common and specific cause of typical
Russell-Silver Syndrome: clinical scoring system and epigenetic-phenotypic
correlations ... Irène Netchine* 1,2,3 , Sylvie Rossignol* 1,2,3 , Marie- ... Cited by 8 - Related articles
- ►endojournals.org G Binder, AK Seidel, K Weber, M Haase, HA … - Journal of Clinical Endocrinology & Metabolism, 2006 - Endocrine Soc Methods: The serum levels of IGF-I, IGF-II, IGF binding protein (IGFBP)-2, and
IGFBP-3 were measured by RIA and compared with age-related reference values and
with serum concentrations measured in age- and gender-matched controls born ... Cited by 17 - Related articles - BL Direct - All 4 versions
J Anderson, D Viskochil, M O'Gorman, C … - American journal of medical genetics, 2002 - interscience.wiley.com Russell-Silver syndrome (RSS) is a genetic syndrome with clinical manifestations
of intrauterine and postnatal growth retardation, normal head circumference,
body asymmetry, and distinctive facial appearance. We followed an infant ... Cited by 9 - Related articles - BL Direct - All 4 versions
MW Moore, LG Dietz, B Tirtorahardjo, PD … - Human mutation, 2003 - interscience.wiley.com Uniparental disomy of chromosome 7 (UPD7) is associated with abnormal phenotypic
effects because of inappropriate expression of imprinted genes on chromosome 7.
Based on the differential methylation of the promoter region of the ... Cited by 10 - Related articles - BL Direct - All 3 versions
S Dörr, M Schlicker, I Hansmann - Human genetics, 2001 - Springer Abstract Human karyopherin α2 (KPNA2), a member of the karyopherin α family,
plays a key role in the nu- clear import of proteins with a classical nuclear
localiza- tion signal (NLS). KPNA2, as part of a karyopherin α-β ... Cited by 3 - Related articles - All 3 versions
SG Kant, AM Van der Weij, W Oostdijk, JM … - Human genetics, 2005 - Springer Abstract Transient neonatal diabetes mellitus (TNDM) is associated with paternal
over-expression of an im- printed locus on chromosome 6q24, which contains one
differentially methylated region (DMR); maternal demethylation at the DMR ... Cited by 3 - Related articles - BL Direct - All 5 versions
