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Browsing by Author Chitayat, D
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Showing results 32 to 37 of 37
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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