Last Updated: 09/26/2026
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Found 15 publications
Silver Russell syndrome in a preterm girl with 8q12.1 deletion encompassing PLAG1.
Journal: Clinical dysmorphology
Published: September 04, 2021
Limb Lengthening in Russell-Silver Syndrome: An Update Confirming Safe and Speedy Healing.
Journal: Journal of pediatric orthopedics
Published: May 17, 2021
The Importance of Collaboration in Advancing Understanding of Rare Disorders: US/EU Joint Initiative on Silver-Russell Syndrome.
Journal: Pediatric endocrinology reviews : PER
Published: January 03, 2018
Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 28, 2017
Effect of Cyproheptadine on Weight and Growth Velocity in Children With Silver-Russell Syndrome.
Journal: Journal of pediatric gastroenterology and nutrition
Published: August 15, 2017
Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
Journal: Journal of medical genetics
Published: July 17, 2017
Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 16, 2017
Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
Journal: Nature reviews. Endocrinology
Published: September 03, 2016
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance.
Journal: Annals of the New York Academy of Sciences
Published: August 21, 2015
Last Updated: 09/26/2026