Results 191 to 200 of about 58,780 (225)
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Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients

Journal of Medical Genetics, 2009
Background Silver–Russell syndrome (SRS, OMIM 180860) features fetal and postnatal growth restriction and variable dysmorphisms. Genetic and epigenetic aberrations on chromosomes 7 and 11 are commonly found in SRS. However, a large fraction of SRS cases remain with unknown genetic aetiology.
Sara, Bruce   +6 more
openaire   +2 more sources

Intellectual functioning in Silver-Russell syndrome: First study in adults

Applied Neuropsychology Adult, 2021
Mélissa Burgevin, Irène Netchine
exaly  

Silver-Russell Syndrome in 2025: Is It Still a Distinct Diagnostic Entity?

Journal of Clinical Endocrinology and Metabolism
É. Giabicani   +2 more
semanticscholar   +1 more source

A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report

HORMONES
Evangelos Bourousis   +4 more
semanticscholar   +1 more source

Silver-Russell syndrome and craniopharyngioma

The Journal of Pediatrics, 1980
M B, Draznin   +2 more
openaire   +2 more sources

[Silver Russell syndrome].

Harefuah, 1984
M, Kleinhaus, J, Arad, Z, Laron
openaire   +1 more source

The search for the gene for Silver-Russell syndrome

Acta Paediatrica, International Journal of Paediatrics, 1999
Philip Stanier
exaly  

Epigenetic and genetic diagnosis of Silver–Russell syndrome

Expert Review of Molecular Diagnostics, 2012
Thomas Eggermann   +2 more
exaly  

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