Meckel Gruber syndrome associated with anencephaly—an unusual reported case
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Embryology,Anatomy
Link
http://academic.oup.com/omcr/article-pdf/2018/2/omx092/23855364/omx092.pdf
Reference10 articles.
1. An unusual case of Meckel–Gruber syndrome (MKS) associated with visceroatrial heterotaxy and facial anomalies;Yuksel;J Obstet Gynaecol (Lahore) [Internet],2016
2. Antenatal ultrasonic diagnosis of Meckel Gruber syndrome (a case report with review of literature);Vernekar;Australas Radiol [Internet],1991
3. Meckel–Gruber syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe;Barisic;Eur J Hum Genet [Internet],2015
4. Meckel Gruber syndrome—a case report;Jeevika;IOSR J Dent Med Sci Ver III [Internet],2016
5. The Meckel syndrome: clinicopathological findings in 67 patients;Salonen;Am J Med Genet [Internet],1984
Cited by 4 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. Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome;Frontiers in Genetics;2023-09-06
2. Structure of the human Meckel-Gruber protein Meckelin;Science Advances;2021-11-05
3. Síndrome Meckel-Gruber: diagnóstico prenatal. Reporte de un caso en el sureste de México;Acta Médica Grupo Ángeles;2020
4. Meckel-Gruber Syndrome: A Case Who Lived for 5 Months;Pediatric Neurosurgery;2019
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