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Showing results 32 to 37 of 37 < previous

	Title	Author(s)	Issue Date
	Renal dysplasia - coarctation of aorta. A new association/syndrome: a report of 6 cases Proceeding/Conference:Annual Meeting of the American Society for Human Genetics, ASHG 2008	Chung, BHY Chitayat, D	2008
	Restrictive dermopathy with massive thrombosis: a previously uncreognized finding Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Hinek, A Chung, BHY Shannon, P Teitelbaum, R Chitayat, D	2009
	Situs inversus totalis in a fetus with a deletion at 7q36.2 detected on microarray analysis Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Andelfinger, G Hitz, MP Keating, S Mercier, J Teitelbaum, R Richter, A Chung, BHY Chitayat, D	2009
	A specific DNA methylation signature associated with NSD1+/- mutations in Sotos syndrome reveals a significant genome-wide loss of DNA methylation (DNAm) targeting CGs in regulatory regions of key developmental genes Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Choufani, S Cytrynbaum, C Turinsky, AL Chen, YA Grafodatskaya, D Xiang, J Feigenberg, M Chung, BHY Stavropoulos, DJ Mendoza-Londono, R Chitayat, D Gibson, WT Reardon, M Brudno, M Weksberg, R	2013
	The first reported case of the dragon gene deletion in human. A case with a de-novo interstitial deletion of chromosome 5Q15-21.1 Proceeding/Conference:30th Annual David W. Smith Workshop	Chitayat, D Chung, BHY Shannon, P Brenner, GJ Toi, A Shaffer, L	2009
	Ulnar-Mammary Syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Jessen, J Chung, BHY Fernandez, B Li, C Chitayat, D	2010

Showing results 32 to 37 of 37 < previous