Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver–Russell Syndrome-Reference-Cited by-同舟云学术

Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver–Russell Syndrome

Published:2021-07-01 Issue:4 Volume:41 Page:401-408
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Kim Soo Yeon¹^ORCID,Shin Chang Ho²^ORCID,Lee Young Ah³^ORCID,Shin Choong Ho³^ORCID,Yang Sei Won³^ORCID,Cho Tae-Joon²^ORCID,Ko Jung Min⁴^ORCID

Affiliation:

1. Pediatric Clinical Neuroscience Center, Department of Pediatrics, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea

2. Division of Pediatric Orthopedics, Department of Orthopaedic Surgery, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea

3. Division of Endocrinology, Department Pediatrics, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea

4. Division of Clinical Genetics, Department of Pediatrics, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea

Funder

Ministry of Education

SNUH research fund

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

http://pdf.medrang.co.kr/ALM/2021/041/ALM041-04-08.pdf

Reference33 articles.

1. Silver HK, Kiyasu W, George J, Deamer WC. Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins. Pediatrics 1953;12:368-76.

2. Russell A. A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples). Proc R Soc Med 1954;47:1040-4.

3. Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients

4. Russell-Silver syndrome

5. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome

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1. Chromosome 7 Isodisomy in a Child with Silver-Russell Síndrome;OBM Genetics;2024-06-24

2. Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome;International Journal of Medical Sciences;2024

3. Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome;Journal of Personalized Medicine;2021-11-13

4. The Methylation Status in the Chromosome 11p15.5 Region and Metabolic Disorders in Children with Syndromic and Nonsyndromic Intrauterine Growth Restriction;Molecular Syndromology;2021-10-12