Holoprosencephaly: report of four cases and genotype–phenotype correlations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s12041-013-0215-5.pdf
Reference19 articles.
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3. Dubourg C., Bendavid C., Pasquier L., Henry C., Odent S. and David V. 2007 Holoprosencephaly. Orphanet J. Rare Dis. 2, 8.
4. Frints S. G., Schoenmakers E. F., Smeets E., Petit P. and Fryns J. P. 1998 De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly. Am. J. Med. Genet. 75, 153–158.
5. Hagan D. M., Ross A. J., Strachan T., Lynch S. A., Ruiz-Perez V., Wang Y. M. et al. 2000 Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. Am. J. Hum. Genet. 66, 1504–1515.
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