Syndromic foramina parietalia permagna
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference20 articles.
1. Congenital Parietal “Foramina” Associated with Faulty Ossification of the Clavicles
2. THE BRANCHIO-SKELETO-GENITAL SYNDROME
3. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss
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2. Craniofacial anomalies, humero-radial synostosis, rhizomelic limb shortness: Previously unrecognized autosomal recessive syndrome;American Journal of Medical Genetics Part A;2007
3. Hereditary cranium bifidum persisting as enlarged parietal foramina (Catlin marks) on cephalometric radiographs;American Journal of Orthodontics and Dentofacial Orthopedics;2006-06
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5. Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype;European Journal of Human Genetics;2005-11-30
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