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4 articles related to "Imprinting Center"

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Articles

Case Report

Published on 15 Nov 2019

Rare De Novo IGF2 Variant on the Paternal Allele in a Patient With Silver–Russell Syndrome

in Genetics of Common and Rare Diseases

Chun-Ling Xia
Yuan Lyu
Chuang Li
Huan Li
Zhi-Tao Zhang
Shao-Wei Yin
Yan Mao
Wen Li
Ling-Yin Kong
Bo Liang

Frontiers in Genetics

doi 10.3389/fgene.2019.01161

6,074 views
8 citations

Original Research

Published on 11 May 2021

A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics

in Genomic Assay Technology

Samuel P. Strom
Waheeda A. Hossain
Melina Grigorian
Mickey Li
Joseph Fierro
William Scaringe
Hai-Yun Yen
Mirandy Teguh
Joanna Liu
Harry Gao

Frontiers in Genetics

doi 10.3389/fgene.2021.608889

9,163 views
29 citations

Review

Published on 26 Apr 2024

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation

in Pediatric Endocrinology

Simona F. Madeo
Luca Zagaroli
Sara Vandelli
Valeria Calcaterra
Antonino Crinò
Luisa De Sanctis
Maria Felicia Faienza
Danilo Fintini
Laura Guazzarotti
Maria Rosaria Licenziati

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1382583

10,565 views
15 citations

Original Research

Published on 24 Aug 2021

Transmission of a Novel Imprinting Center Deletion Associated With Prader–Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About

in Genetics of Common and Rare Diseases

Kaihui Zhang
Shu Liu
Wenjun Gu
Yuqiang Lv
Haihua Yu
Min Gao
Dong Wang
Jianyuan Zhao
Xiaoying Li
Zhongtao Gai

Frontiers in Genetics

doi 10.3389/fgene.2021.630650

8,078 views
2 citations