Author:
Berrada Sarah,Tazzite Amal,Bouzroud Wafaa,Gazzaz Bouchaib,Lehlimi Mouna,Dehbi Hind
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health
Reference9 articles.
1. FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome.;Alazami;Am J Hum Genet,2009
2. Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.;Beck;Hum Mol Genet,2013
3. Novel FREM1 mutations in a patient with MOTA syndrome: clinical findings, mutation update and review of FREM1-related disorders literature.;Chacon-Camacho;Eur J Med Genet,2017
4. Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly.;Dawson;Clin Dysmorphol,2021
5. The median cleft face syndrome. Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate.;DeMyer;Neurology,1967
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