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Browsing by Author Tong, TMF
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Showing results 2 to 14 of 14
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Title
Author(s)
Issue Date
Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong
Journal:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Yu, KPT
Luk, HM
Leung, KC
Mak, CCY
Cheng, SSW
Hau, EWL
Chan, DKH
Lam, STS
Tong, TMF
Chung, BHY
Lo, FMI
2019
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
HUGO / HUGO-AP 2006
Lun, KS
Lam, STS
Tong, TMF
Chung, BHY
Li, YH
Chan, HC
Or, SF
Lau, YL
2006
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
Annual Congress of the Asian Society for Pediatric Research, ASPR 2006
Chung, BHY
Lam, STS
Tong, TMF
Li, YH
Lun, KS
Chan, HC
Or, SF
Lau, YL
2006
Identification of 25 novel and 2 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
HKPS-HKPNA 2006 Joint Annual Scientific Meeting
Chung, BHY
Lam, STS
Tong, TMF
Li, YH
Lun, KS
Chan, HC
Or, SF
Lau, YL
2006
Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes
Journal:
American Journal of Medical Genetics, Part A
Chung, BHY
Lam, STS
Tong, TMF
Li, SYH
Lun, KS
Chan, DHC
Fok, SFS
Or, JSF
Smith, DK
Yang, W
Lau, YL
2009
Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T>A and 79G>T in RMRP gene
Journal:
Prenatal Diagnosis
Lam, ACF
Chan, DHC
Tong, TMF
Tang, MHY
Lo, SYF
Lo, IFM
Lam, STS
2006
Molecular defects in haemophilia B: Detection by direct restriction enzyme analysis
Journal:
British Journal of Haematology
Chan, V
Yip, B
Tong, TMF
Chan, TPT
Lau, K
Yam, I
Chan, TK
1991
Multiple Xba I polymorphisms in Haemophilia A (I: Reply)
Journal:
British Journal of Haematology
Chan, V
Tong, TMF
Chan, TK
1990
Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A
Journal:
British Journal of Haematology
Chan, V
Tong, TMF
Chan, TPT
Tang, M
Wan, CW
Chan, FY
Chu, YC
Chan, TK
1989
A novel missense mutation in exon 4 of the factor VIII:C gene resulting in moderately severe hemophilia A
Journal:
Blood
Chan, V
Chan, TK
Tong, TMF
Todd, D
1989
Silver-Russell syndrome in Hong Kong
Journal:
Hong Kong Medical Journal
Luk, HM
YEUNG, KS
Wong, WL
Chung, BHY
Tong, TMF
Lo, IFM
2016
Thanatophoric dysplasia variant, San Diego type in a Chinese fetus, caused by C746G missense mutation in FGFR3 gene
Journal:
Hong Kong Journal of Paediatrics
Lam, ACF
Tong, TMF
Tang, MHY
Lo, S
Lee, CP
Lau, E
Lam, STS
2006
Two cases of spondylothoracic dysostosis (Jarcho Levin syndrome) in Chinese population
Proceeding/Conference:
Asia Pacific Conference on Human Genetics, 2010
Lai, CWS
Lau, EWL
Lo, IFM
Chiu, WK
Law, CW
Tong, TMF
Lam, STS
2011