Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study-Reference-Cited by-同舟云学术

Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study

Published:2018-09 Issue:9 Volume:61 Page:483-488
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Garne Ester,Rissmann Anke^ORCID,Addor Marie-Claude,Barisic Ingeborg,Bergman Jorieke^ORCID,Braz Paula,Cavero-Carbonell Clara^ORCID,Draper Elizabeth S.,Gatt Miriam,Haeusler Martin,Klungsoyr Kari,Kurinczuk Jennifer J.,Lelong Nathalie,Luyt Karen,Lynch Catherine,O'Mahony Mary T.,Mokoroa Olatz^ORCID,Nelen Vera,Neville Amanda J.,Pierini Anna^ORCID,Randrianaivo Hanitra,Rankin Judith,Rouget Florence,Schaub Bruno^ORCID,Tucker David,Verellen-Dumoulin Christine,Wellesley Diana,Wiesel Awi,Zymak-Zakutnia Nataliia,Lanzoni Monica,Morris Joan K.^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference25 articles.

1. Septo-optic dysplasia: antenatal risk factors and clinical features in a regional study;Atapattu;Horm. Res. Paediatr.,2012

2. The EUROCAT network: organisation and processes;Boyd;Birth Defects Res. A Clin. Mol. Teratol.,2011

3. Maternal age re septo-optic dysplasia;Elster;J. Pediatr.,1979

4. EUROCAT Guide 1.4,2017

5. Septo-optic dysplasia;Fard;Ped. Endocrinol. Rev.,2010

Cited by 32 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. Septo-optic dysplasia plus syndrome in a 2-year-old child: A case report;Radiology Case Reports;2024-09

2. Gastroschisis and septo‐optic‐pituitary dysplasia: Is there an association?;Journal of Paediatrics and Child Health;2024-05-23

3. Co-occurrence of Attention-Deficit/Hyperactivity Disorder and Septo-Optic Dysplasia: A Neurodevelopmental Case Report;Cureus;2024-05-16

4. Segmental Agenesis of the Corpus Callosum With Pituitary Hypoplasia;Cureus;2024-04-22

5. Updated EUROCAT guidelines for classification of cases with congenital anomalies;Birth Defects Research;2024-02