Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations
Author:
Funder
Deutsche Forschungsgemeinschaft
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference19 articles.
1. Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction;Abi Habib;Genet. Med.,2018
2. A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome;Azzi;J. Med. Genet.,2015
3. GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion;Blagitko;Hum. Mol. Genet.,2000
4. Microdeletions of the 7q32.2 imprinted region are associated with Silver-Russell syndrome features;Carrera;Am. J. Med. Genet. A,2016
5. Interactions between imprinting effects in the mouse;Cattanach;Genetics,2004
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2. Effects of Developmental Lead and Phthalate Exposures on DNA Methylation in Adult Mouse Blood, Brain, and Liver: A Focus on Genomic Imprinting by Tissue and Sex;Environmental Health Perspectives;2024-06
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4. Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith–Wiedemann spectrum features;Molecular Case Studies;2021-10-06
5. Segmental maternal uniparental disomy of chromosome 7q in a patient with congenital chloride diarrhea;Journal of Clinical Laboratory Analysis;2021-06-04
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