HKU Scholars Hub: Browsing DSpace

Browsing by Author Burzynski, G

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 1 to 8 of 8

	Title	Author(s)	Issue Date
	Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liability Journal:American Journal of Human Genetics	Emison, ES GarciaBarcelo, M Grice, EA Lantieri, F Amiel, J Burzynski, G Fernandez, RM Hao, L Kashuk, C West, K Miao, X Tam, PKH Griseri, P Ceccherini, I Pelet, A Jannot, AS De Pontual, L HenrionCaude, A Lyonnet, S Verheij, JBGM Hofstra, RMW Antiñolo, G Borrego, S McCallion, AS Chakravarti, A	2010
	Differential liabilities of coding and non-coding mutations in complex disease Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2005	Burzynski, G Amiel, J Antinolo, G Borrego,, S Ceccherini, I Emison, E Eng, C Fernandez, R Garcia-Barcelo, MM Griseri, P Hofstra, R Kashuk, C Lantieri, F Lyonnet, S Tam, PKH Tullio-Pelet, A West, K Chakravarti, A	2005
	Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung diseases Proceeding/Conference:GRC on Human Genetics & Genomics	Emison, E Burzynski, G Amiel, J Borrego, S Ceccherini,, I Fernandez, R Garcia-Barcelo, MM Griseri, P Hofstra, R Kashuk, CS Lantieri, F Lyonnet, S Tam, PKH Pecina, A Tullio-Pelet,, A West, K Chakravarti, A	2005
	Fine mapping of the 9q31 Hirschsprung's disease locus Journal:Human Genetics	Tang, CS Sribudiani, Y Miao, XP De Vries, AR Burzynski, G So, MT Leon, YY Yip, BH Osinga, J Hui, KJWS Verheij, JBGM Cherny, SS Tam, PKH Sham, PC Hofstra, RMW GarciaBarceló, MM	2010
	Higher prevalence of Hirschsprung disease in China explained by a common RET mutation Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006	Garcia-Barcelo, MM Amiel, J Antinolo, G Borrego, S Burzynski, G Ceccherini, I Emison, E Eng, C Fernandez, R Griseri, P Hofstra, R Kashuk, C Lantien, F Lyonnet, S Miao, X Tam, PKH Tullio-Pelet, A West, K Chakravarti, A	2006
	Hirschsprung disease, associated syndromes and genetics: A review Journal:Journal of Medical Genetics	Amiel, J SproatEmison, E GarciaBarcelo, M Lantieri, F Burzynski, G Borrego, S Pelet, A Arnold, S Miao, X Griseri, P Brooks, AS Antinolo, G De Pontual, L ClementZiza, M Munnich, A Kashuk, C West, K Wong, KKY Lyonnet, S Chakravarti, A Tam, PKH Ceccherini, I Hofstra, RMW Fernandez, R	2008
	The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease Proceeding/Conference:Annual International Congress of the British Association of Paediatric Suregons, BAPS 2006	Tam, PKH Garcia-Barcelo, MM Tullio-Pelet, A Lyonnet, S Lantieri, F Kashuk, C Hofstra, R Griseri, P Fernandez, R Eng, C Emison, E Burzynski, G Ceccherini, I Borrego, S Antinolo, G Amiel, J West, K Chakravarti, A	2006
	Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease Journal:Human Molecular Genetics	Tang, SM Gui, H Kapoor, A Kim, JH Luzon-Toro, B Pelet, A Burzynski, G Lantieri, F So, MT Berrios, C Shin, HD Fernandez, RM Le, TL Verheij, JBGM Matera, I Cherny, SS Nandakumar, P Cheong, HS Antinolo, G Amiel, J Seo, JM Kim, DY Oh, JT Lyonnet, S Borrego, S Ceccherini, I Hofstra, RMW Chakravarti, A Kim, HY Sham, PC Tam, PKH Garcia-Barcelo, MM	2016

Showing results 1 to 8 of 8