PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01730.x/fullpdf
Reference15 articles.
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2. Prenatal diagnosis and molecular genetic studies on a new case of agnathia-otocephaly.;Kamnasaran;Fetal Pediatr Pathol,2010
3. An anatomical study of human otocephaly.;Lawrence;Teratology,1984
4. Otocephaly: report of five new cases and a literature review.;Faye-Petersen;Fetal Pediatr Pathol,2006
5. Familial agnathia - holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance.;Krassikoff;Am J Med Genet,1989
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