Silver-Russell syndrome (SRS) is a growth retardation syndrome in which loss of methylation on chromosome 11p15 (11p15 LOM) and maternal uniparental disomy for chromosome 7 [UPD(7) mat] explain 20-60% and 10% of the syndrome, respectively. To search for a molecular cause for the remaining SRS cases, and to find a possible common epigenetic change, we studied DNA methylation pattern of more than 450 000 CpG sites in 44 SRS patients. Common to all three SRS subgroups, we found a hypomethylated region at the promoter region of HOXA4 in 55% of the patients. We then tested 39 patients with severe growth restriction of unknown etiology, and found hypomethylation of HOXA4 in 44% of the patients. Finally, we found that methylation at multiple CpG s...
BACKGROUND: Silver-Russell syndrome (SRS; online inheritance in man 180860) is a low-birth-weight sy...
Silver–Russell syndrome (SRS) is characterised by prenatal and postnatal growth retardation, dysmorp...
International audienceContext - Silver-Russell syndrome (SRS) (mainly secondary to 11p15 molecular d...
A combination of genes, their epigenetic regulation, and the environment control the phenotypes of a...
BACKGROUND: Silver-Russell syndrome (SRS) is a clinically and genetically heterogeneous condition ch...
The H19 differentially methylated region (DMR) controls the allele-specific expression of both the i...
Silver?Russell syndrome (SRS) is a congenital developmental disorder characterized by intrauterine a...
Silver-Russell syndrome is an imprinting disorder characterised by pre- and post-natal growth retard...
This study was an investigation of 79 patients referred to the Wessex Regional Genetics Laboratory w...
<div><p>Background</p><p>Recent studies have revealed relative frequency and characteristic phenotyp...
textabstractBackground: Silver-Russell syndrome (SRS; online inheritance in man 180860) is a low-bir...
BACKGROUND: Silver-Russell syndrome (SRS) is a genetically and clinically heterogeneous disease. Alt...
BACKGROUND: Silver-Russell syndrome (SRS; online inheritance in man 180860) is a low-birth-weight sy...
Silver–Russell syndrome (SRS) is characterised by prenatal and postnatal growth retardation, dysmorp...
International audienceContext - Silver-Russell syndrome (SRS) (mainly secondary to 11p15 molecular d...
A combination of genes, their epigenetic regulation, and the environment control the phenotypes of a...
BACKGROUND: Silver-Russell syndrome (SRS) is a clinically and genetically heterogeneous condition ch...
The H19 differentially methylated region (DMR) controls the allele-specific expression of both the i...
Silver?Russell syndrome (SRS) is a congenital developmental disorder characterized by intrauterine a...
Silver-Russell syndrome is an imprinting disorder characterised by pre- and post-natal growth retard...
This study was an investigation of 79 patients referred to the Wessex Regional Genetics Laboratory w...
<div><p>Background</p><p>Recent studies have revealed relative frequency and characteristic phenotyp...
textabstractBackground: Silver-Russell syndrome (SRS; online inheritance in man 180860) is a low-bir...
BACKGROUND: Silver-Russell syndrome (SRS) is a genetically and clinically heterogeneous disease. Alt...
BACKGROUND: Silver-Russell syndrome (SRS; online inheritance in man 180860) is a low-birth-weight sy...
Silver–Russell syndrome (SRS) is characterised by prenatal and postnatal growth retardation, dysmorp...
International audienceContext - Silver-Russell syndrome (SRS) (mainly secondary to 11p15 molecular d...