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Engle Lab Publications
The best way to find out about recent research on strabismus and congenital cranial dysinnervation disorders (CCDD's) is to search medical and biology journals through the National Institute of Health's "PubMed" Web site. This will provide you with access to every abstract that has been published, you simply need to type in a keyword to direct you to the associated articles.

You and your physician can also get up-to-date information on CCDD's by contacting us directly.

The files listed below allow access to some key publications that have been authored by members of our laboratory.

Identification of the HOXA1gene in Duane syndrome type III, with associated hearing and vascular abnormalities-Nat Genet. 2005 Sep 11.
Identification of CFEOM1 gene-Nat Genet. 2003 Dec;35(4):318-21.
KIF21A mutation analysis of CFEOM3 individuals-Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23.
Identification of Duane syndrome with radial ray anomalies gene- Am J Hum Genet. 2002 Nov;71(5):1195-9.
Identification of the CFEOM2 gene-Nature Genetics, 2001 Nov;29(3):315-20.
Mapping of a congenital ptosis gene to a region on Chromosome 1-Am J Hum Genet. 1997 May;60(5):1150-7.
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