A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases Registration-Reference-Cited by-同舟云学术

A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases Registration

Published:2018-09 Issue:9 Volume:61 Page:513-517
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Kinsner-Ovaskainen Agnieszka^ORCID,Lanzoni Monica,Garne Ester,Loane Maria,Morris Joan,Neville Amanda,Nicholl Ciarán,Rankin Judith,Rissmann Anke^ORCID,Tucker David,Martin Simona

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference15 articles.

1. Paper 1: the EUROCAT network: organization and processes;Boyd;Bir. Def. Res. (Part A),2011

2. Complete list of EUROCAT members. Retrieved 22 February 23, 2018, from EUROCAT: http://www.eurocat-network.eu/pagecontent.aspx?tree=allmembers, (Accessed 23.02.2018).

3. EDMP User Guide. Retrieved 22 February 23, 2018, from EUROCAT: http://www.eurocat-network.eu/content/Section%202.4-%2027_Oct2016.pdf.

4. EUROCAT Guide 1.4. (2016). Retrieved 22 February 23, 2018: www.eurocat-network.eu/aboutus/datacollection/guidelinesforregistration/guide1_4.

5. EUROCAT Membership Criteria, Retrieved 22 February 23, 2018, from EUROCAT: http://www.eurocat-network.eu/content/Membership%20criteria_vs, (Accessed 23.02.2018).

Cited by 48 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. High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant inIRF6;2024-07-10

2. Orofacial Clefts and Maternal Risk Factors: A Population-Based Case–Control Study;Children;2024-07-04

3. Scoping review of the recommendations and guidance for improving the quality of rare disease registries;Orphanet Journal of Rare Diseases;2024-05-06

4. Hypothyroidism in Patients with Down Syndrome: Prevalence and Association with Congenital Heart Defects;Children;2024-04-25

5. Academic achievement at ages 11 and 16 in children born with congenital anomalies in England: A multi‐registry linked cohort study;Paediatric and Perinatal Epidemiology;2024-02-06