Articles

Prenatal diagnosis of a silver-russell syndrome caused by 11p15 duplication and pedigree analysis

in Genetics of Common and Rare Diseases

• Shurong Hong
• Hua Wei
• Xueyi Zhuang
• Weirong Huang
• Yu Zhang

Diagnosis and Management of Beckwith-Wiedemann Syndrome

in Genetics of Common and Rare Diseases

• Kathleen H. Wang
• Jonida Kupa
• Kelly A. Duffy
• Jennifer M. Kalish

Prenatal Diagnosis of a Mosaic Paternal Uniparental Disomy for Chromosome 14: A Case Report of Kagami–Ogata Syndrome

in Genetics of Common and Rare Diseases

• Fenxia Li
• Siping Liu
• Bei Jia
• Ruifeng Wu
• Qingxian Chang

Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome

in Pediatric Endocrinology

• Petra Loid
• Marita Lipsanen-Nyman
• Sirpa Ala-Mello
• Katariina Hannula-Jouppi
• Juha Kere
• Outi Mäkitie
• Mari Muurinen

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features

in Genetics of Common and Rare Diseases

• Valentina Cirello
• Valentina Giorgini
• Chiara Castronovo
• Susan Marelli
• Ester Mainini
• Alessandra Sironi
• Maria Paola Recalcati
• Marco Pessina
• Daniela Giardino
• Lidia Larizza

Case Report: Beckwith–Wiedemann syndrome with reduced H19 expression

in Children and Health

• Meng Wang
• Jiegang Deng
• Shuhua Xing
• Xuening Niu

Case Report: Liraglutide for Weight Management in Beckwith-Wiedemann Syndromic Obesity

in Obesity

• Marina Caputo
• Tommaso Daffara
• Simonetta Bellone
• Valentina Mancioppi
• Paolo Marzullo
• Gianluca Aimaretti
• Flavia Prodam

Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylation

in Neonatology

• Diane Darneau
• Eloïse Giabicani
• Irène Netchine
• Aurélie Pham

A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation

in Genetics of Common and Rare Diseases

• Xiaoxue Wang
• Hui Pang
• Birju A. Shah
• Hongcang Gu
• Lijun Zhang
• Hua Wang

Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

in Systems Endocrinology

• Milena Crippa
• Maria Teresa Bonati
• Luciano Calzari
• Chiara Picinelli
• Cristina Gervasini
• Alessandra Sironi
• Ilaria Bestetti
• Sara Guzzetti
• Simonetta Bellone
• Angelo Selicorni

Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome

in Neuroendocrine Science

• Régis Afonso Costa
• Igor Ribeiro Ferreira
• Hiago Azevedo Cintra
• Leonardo Henrique Ferreira Gomes
• Letícia da Cunha Guida

Alteration of brain nuclei in obese children with and without Prader-Willi syndrome

• Ning Wu
• Huan Yu
• Mingze Xu