Nissen fundoplication in Cornelia de Lange syndrome spectrum: Who are the potential candidates?-Reference-Cited by-同舟云学术

Nissen fundoplication in Cornelia de Lange syndrome spectrum: Who are the potential candidates?

Published:2020-05-21 Issue:7 Volume:182 Page:1697-1703
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Parma Barbara¹,Cianci Paola¹²^ORCID,Mariani Milena¹³,Cereda Anna⁴,Panceri Roberto⁵,Fossati Chiara³⁵,Maestri Luciano⁶,Macchini Francesco⁷,Onesimo Roberta⁸,Zampino Giuseppe⁸^ORCID,Betalli Pietro⁹,Cheli Maurizio⁹,Selicorni Angelo¹^ORCID

Affiliation:

1. Department of Pediatrics ASST‐Lariana, "Sant'Anna" Hospital Como Italy

2. Woman and Child Department “F. Del Ponte” Hospital, University of Insubria Varese Italy

3. Clinical Paediatric Genetics Unit, MBBM Foundation “S. Gerardo” Hospital Monza Italy

4. Department of Pediatrics ASST Papa Giovanni XXIII Bergamo Italy

5. Department of Pediatrics, MBBM Foundation “S.Gerardo” Hospital Monza Italy

6. Pediatric Surgery Department “V. Buzzi” Children's Hospital, ASST Fatebenefratelli‐Sacco Milan Italy

7. Department of Pediatric Surgery Fondazione Ca' Granda Ospedale Maggiore Policlinico, IRCCS Milan Italy

8. Center for Rare Diseases and Birth Defects, Woman and Child Department Fondazione Policlinico Universitario “A. Gemelli”, IRCCS Rome Italy

9. Department of Pediatric Surgery ASST Papa Giovanni XXIII Bergamo Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61625

Reference32 articles.

1. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience

2. Congenital diaphragmatic hernia in the Brachmann-de Lange syndrome

3. Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation

4. RAD21 Mutations Cause a Human Cohesinopathy

5. NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations

Cited by 2 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. Sleep correlates of behavior functioning in Cornelia de Lange syndrome;American Journal of Medical Genetics Part A;2024-06-22

2. The Impact of Blenderized Tube Feeding on Gastrointestinal Symptoms, a Scoping Review;Applied Sciences;2023-02-08