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Browsing "Department of Paediatrics & Adolescent Medicine" by Author li, yh
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Showing results 1 to 11 of 11
Title
Author(s)
Issue Date
ADAMTS13 mutational analysis in Chinese patients with chronic relapsing thrombotic thrombocytopenic purpura
Journal:
Hong Kong Journal of Paediatrics
Ma, ESK
Li, YH
Kwok, JSY
Ling, SC
Yau, PW
Chan, GCF
2006
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 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC)
Proceeding/Conference:
International Congress of Pediatrics, IPA 2007
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2007
Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC
Proceeding/Conference:
Congress of Asian Society for Pediatric Research, ASPR 2007
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2007
Identification of 7 novel transforming growth factor β receptor 2 mutations in Chinese patients with marfan syndrome
Proceeding/Conference:
Pediatrics
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2008
Long term immune reconstitution after Bone Marrow Transplantation for severe combined immunodeficiency and Wiskott Aldrich Syndrome
Proceeding/Conference:
Guangdong-Hong Kong 2004 Paediatrics Exchange Meeting
Chiang, AKS
Ma, ESK
Jones, BM
Li, YH
Chan, GCF
Ha, SY
Lau, YL
2004
Long term immune reconstitution and cell lineage chimerism after bone marrow transplantation for severe combined immunodeficiency and Wiskott-Aldrich Syndrome
Proceeding/Conference:
Blood
Chiang, AKS
Ma, ESK
Jones, BM
Li, YH
Chan, GCF
Ha, SY
Lau, YL
2002
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease type A (NPD-A)
Proceeding/Conference:
HKPS-HKPNA 2006 Joint Annual Scientific Meeting
Chung, BHY
Fung, CW
Li, YH
Wong, KY
Chan, GCF
Wong, VCN
2006
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease Type A (NPD-A)
Proceeding/Conference:
50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation
Chung, BHY
Fung, CW
Li, YH
Wong, KY
Chan, GCF
Wong, VCN
2005