Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum.

The Journal of clinical endocrinology and metabolism - 8 Mar 2021

Fuke Tomoko, Nakamura Akie, Inoue Takanobu, Kawashima Sayaka, Hara Kaori Isono, Matsubara Keiko, Sano Shinichiro, Yamazawa Kazuki, Fukami Maki, Ogata Tsutomu, Kagami Masayo

Abstract excerpt

BACKGROUND: (Epi)genetic disorders associated with small-for-gestational-age with short stature (SGA-SS) include imprinting disorders (IDs). Silver-Russell syndrome (SRS) is a representative ID in SGA-SS and has heterogenous (epi)genetic causes. SUBJECTS AND METHODS: To clarify the contribution of IDs to SGA-SS and the molecular and phenotypic spectrum of SRS, we recruited 269 patients with SGA-SS, consisting of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Comparative Genomic Hybridization
Share to Dwarfism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to Genomic Imprinting

Share to Human Growth Hormone

Share to Infant, Small for Gestational Age

Share to Microcephaly

Share to Silver-Russell Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 33236057
DOI: 10.1210/clinem/dgaa856
PMCID: PMC7947753

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum.PMID 33236057Read ↗

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting DisordersSemantic proximity Read ↗

New clinical and molecular insights into Silver-Russell syndrome.Semantic proximity Read ↗

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.Semantic proximity Read ↗

Frequency and characterization of DNA methylation defects in children born SGA.Semantic proximity Read ↗

Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular EtiologySemantic proximity Read ↗

Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.Semantic proximity Read ↗

Silver-Russell syndrome.Semantic proximity Read ↗

New Developments in Silver–Russell Syndrome and Implications for Clinical PracticeSemantic proximity Read ↗

Approach to the Patient With Suspected Silver-Russell SyndromeSemantic proximity Read ↗

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome.Semantic proximity Read ↗

Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome.Semantic proximity Read ↗

The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short StatureSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.