A new autosomal recessive syndrome of ocular colobomas, ichthyosis, brain malformations and endocrine abnormalities in an inbred Emirati family
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference21 articles.
1. Septo-Optic Dysplasia in Two Siblings
2. Hypopituitarism and septooptic “dysplasia” in first cousins
3. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
4. Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes
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