Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology-Reference-Cited by-同舟云学术

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Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology

Published:2016 Issue:3 Volume:7 Page:110-121
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Õunap Katrin

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Silver-Russell syndrome-like features in a child with recombinant chromosome 11 derived from maternal pericentric inversion;Clinical Dysmorphology;2024-05-29

2. Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report;World Journal of Clinical Cases;2024-03-16

3. Graph Self-Supervised Learning With Application to Brain Networks Analysis;IEEE Journal of Biomedical and Health Informatics;2023-08

4. Epigenetic regulation of gene expression: an overview of classical and recently discovered novel players;Perinatal and Developmental Epigenetics;2023

5. Understanding Prenatal and Postnatal Linear Growth;The Journal of Clinical Endocrinology & Metabolism;2022-10-17

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