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- [31] ICR1 epimutations in 11p15 are restricted to patients with Silver-Russell syndrome features JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2008, 21 (01): : 59 - 62
- [32] Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2024,
- [33] LOT1 (ZAC1/PLAGL1) as Member of an Imprinted Gene Network Does Not Harbor Silver-Russell Specific Variants JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2009, 22 (06): : 555 - 559
- [35] A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2024, 23 (03): : 591 - 593
- [36] Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers European Journal of Human Genetics, 2019, 27 : 42 - 48
- [40] Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7 FRONTIERS IN ENDOCRINOLOGY, 2024, 15