6 results on '"Spengler, S."'
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2. Isolated hypermethylation of GRB10 (7p12.2) in a Silver–Russell syndrome patient carrying a 20p13 microdeletion
3. Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver–Russell syndrome features
4. Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues
5. Submicroscopic chromosomal imbalances in idiopathic Silver–Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome
6. Severe headache associated with occupational exposure to Stoddard solvent
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