Author:
Azimi Cyrus,Kennedy Shelley J.,Chitayat David,Chakraborty Pranesh,Clarke Joe T.R.,Forrest Christopher,Teebi Ahmad S.
Subject
Genetics (clinical),Genetics
Reference41 articles.
1. Trigonomicrocephaly, severe micrognathia, large ears, atrioventricular septal defects, symmetrical cutaneous syndactyly of hands and feet, and multiple café-au-lait spots: New acrocraniofacial dysostosis syndrome?;Al-Sannaa;Am J Med Genet,2001
2. Craniosynostosis. A survey of 204 cases;Anderson;J Neurosurg,1965
3. Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome;Christ;Am J Hum Genet,1999
4. X-linked skeletal dysplasia with mental retardation;Christian;Clin Genet,1977
5. FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype;Chu;Am J Med Genet,1994
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