Nonsyndromal anencephaly: Possible autosomal recessive variant

Author:

Farag Talaat I.,Teebi Ahmad S.,Al-Awadi Sadika A.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Cited by 18 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. A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family;Human Molecular Genetics;2017-01-13

2. Genetic Disorders in Kuwait;Genetic Disorders Among Arab Populations;2010

3. Epidemiology of neural tube defects;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2005

4. Congenital Developmental Anomalies;Genetic Disorders of the Indian Subcontinent;2004

5. Dichorionic triplet pregnancy with the monoamniotic twin pair concordant for omphalocele and bladder exstrophy;Ultrasound in Obstetrics and Gynecology;2000-12

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