Fetal growth patterns in Beckwith-Wiedemann syndrome-Reference-Cited by-同舟云学术

Fetal growth patterns in Beckwith-Wiedemann syndrome

Published:2016-03-15 Issue:1 Volume:90 Page:21-27
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Mussa A.¹^ORCID,Russo S.²,de Crescenzo A.³,Freschi A.³,Calzari L.²,Maitz S.⁴,Macchiaiolo M.⁵,Molinatto C.¹,Baldassarre G.¹,Mariani M.⁴,Tarani L.⁶,Bedeschi M.F.⁷,Milani D.⁸,Melis D.⁹,Bartuli A.⁵,Cubellis M.V.¹⁰,Selicorni A.⁴,Silengo M.C.¹,Larizza L.²,Riccio A.³¹¹,Ferrero G.B.¹

Affiliation:

1. Department of Pediatric and Public Health Sciences; University of Turin; Turin Italy

2. Laboratory of Cytogenetics and Molecular Genetics; Istituto Auxologico Italiano; Milan Italy

3. DiSTABiF; Second University of Naples; Naples Italy

4. Clinical Pediatric Genetics Unit, Pediatrics Clinics; MBBM Foundation, S. Gerardo Hospital; Monza Italia

5. Rare Disease and Medical Genetics Unit; Bambino Gesù Children Hospital; Rome Italy

6. Department of Pediatric and Pediatric Neuropsychiatry; Sapienza University; Rome Italy

7. Medical Genetics Unit, IRCCS Ca' Granda Foundation; Ospedale Maggiore Policlinico; Milan Italy

8. Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation; Università degli Studi di Milano Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Milan Italy

9. Clinical Pediatric Genetics, Department of Pediatrics; University “Federico II”; Naples Italy

10. Department of Biology; University of Naples Federico II; Naples Italy

11. Institute of Genetics and Biophysics “A. Buzzati-Traverso” - CNR; Naples Italy

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Telethon-Italia

EU-FP7-ITN INGENIUM

Progetto Bandiera MIUR-CNR Epigenomica and Associazione Italiana Ricerca sul Cancro

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference45 articles.

1. Prevalence of Beckwith-Wiedemann syndrome in North West of Italy;Mussa;Am J Med Genet A,2013

2. Clinical utility gene card for: Beckwith-Wiedemann Syndrome;Eggermann;Eur J Hum Genet,2014

3. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome;Sparago;Nat Genet,2004

4. Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour;Sparago;Hum Mol Genet,2007

Cited by 35 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. Development of disease‐specific growth charts for Korean children with Beckwith–Wiedemann syndrome;Clinical Genetics;2024-01-24

2. Occurrence of Hepatoblastomas in Patients with Beckwith–Wiedemann Spectrum (BWSp);Cancers;2023-04-29

3. Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians;International Journal of Environmental Research and Public Health;2022-02-20

4. Guided Growth in Leg Length Discrepancy in Beckwith-Wiedemann Syndrome: A Consecutive Case Series;Children;2021-12-07

5. Lateralized and Segmental Overgrowth in Children;Cancers;2021-12-07