Russell-Silver Dwarfism Latest Advances

Find the Latest Research About Russell-Silver Dwarfism

Last Updated: 09/19/2026

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Found 612 publications

Culture-dependent decoupling of H19 allele-specific expression from H19/IGF2:IG-DMR methylation in experimental models.

Culture-dependent decoupling of H19 allele-specific expression from H19/IGF2:IG-DMR methylation in experimental models.

Journal: Epigenetics

Published: July 30, 2026

Anosmia in a patient with Silver-Russell syndrome.

Anosmia in a patient with Silver-Russell syndrome.

Journal: BMJ case reports

Published: June 01, 2026

Mechanisms controlling genomic imprinting and their dysregulation in human imprinting disorders.

Mechanisms controlling genomic imprinting and their dysregulation in human imprinting disorders.

Journal: Annales d'endocrinologie

Published: April 17, 2026

Clinical and genetic analysis of children with Silver-Russell syndrome

Clinical and genetic analysis of children with Silver-Russell syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 01, 2026

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Journal: Fetal diagnosis and therapy

Published: March 20, 2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Journal: Clinical genetics

Published: January 28, 2026

Comparison of bone age between both limbs in patients with congenital hemihyperplasia or hemihypoplasia: A retrospective study.

Comparison of bone age between both limbs in patients with congenital hemihyperplasia or hemihypoplasia: A retrospective study.

Journal: Journal of children's orthopaedics

Published: January 16, 2026

Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes.

Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes.

Journal: Human genomics

Published: December 09, 2025

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Journal: Clinical genetics

Published: October 30, 2025

Assessment of combined growth hormone and gonadotropin-releasing hormone analogue treatment in children with Silver-Russell syndrome.

Assessment of combined growth hormone and gonadotropin-releasing hormone analogue treatment in children with Silver-Russell syndrome.

Journal: Hormone research in paediatrics

Published: October 17, 2025

Temple Syndrome Is a Frequent Differential Diagnosis of Silver-Russell Syndrome, but Infrequently Suspected in Chile.

Temple Syndrome Is a Frequent Differential Diagnosis of Silver-Russell Syndrome, but Infrequently Suspected in Chile.

Journal: American journal of medical genetics. Part A

Published: October 07, 2025

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Journal: Clinical epigenetics

Published: September 23, 2025

Showing 1-12 of 612

Last Updated: 09/19/2026