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Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
September 19, 2001
Proteus syndrome: a case report
S Pangkanon, W Limpongsanurak, V Sangtawesin
The Southeast Asian Journal of Tropical Medicine and Public Health
|
October 22, 2009
Detection of phenylketonuria by the newborn screening program in Thailand
S Pangkanon, W Charoensiriwatana, N Janejai, et al.
American Journal of Medical Genetics
|
November 11, 1996
Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature
J Leana-Cox, S Pangkanon, K R Eanet, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
April 6, 2001
Establishing gas chromatography-mass spectrometry to diagnose organic acidemias in Thailand
V Shotelersuk, S Srivuthana, S Wacharasindhu, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
February 21, 2002
Normal plasma free amino acid levels in Thai children
J Svasti, P Wasant, M Tiensuwan, et al.
Blood Cells, Molecules & Diseases
|
August 11, 2007
Molecular characterization of type 3 (neuronopathic) Gaucher disease in Thai patients
P Suwannarat, S Keeratichamroen, D Wattanasirichaigoon, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome
S Keeratichamroen, J R Ketudat Cairns, D Wattanasirichaigoon, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
September 19, 2001
Proteus syndrome: a case report
S Pangkanon, W Limpongsanurak, V Sangtawesin
The Southeast Asian Journal of Tropical Medicine and Public Health
|
October 22, 2009
Detection of phenylketonuria by the newborn screening program in Thailand
S Pangkanon, W Charoensiriwatana, N Janejai, et al.
American Journal of Medical Genetics
|
November 11, 1996
Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature
J Leana-Cox, S Pangkanon, K R Eanet, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
April 6, 2001
Establishing gas chromatography-mass spectrometry to diagnose organic acidemias in Thailand
V Shotelersuk, S Srivuthana, S Wacharasindhu, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
February 21, 2002
Normal plasma free amino acid levels in Thai children
J Svasti, P Wasant, M Tiensuwan, et al.
Blood Cells, Molecules & Diseases
|
August 11, 2007
Molecular characterization of type 3 (neuronopathic) Gaucher disease in Thai patients
P Suwannarat, S Keeratichamroen, D Wattanasirichaigoon, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome
S Keeratichamroen, J R Ketudat Cairns, D Wattanasirichaigoon, et al.
Page
of 1