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Showing results for
cheng anna w[au]
Your search for
Cheng Ann AG[au]
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Genital anomalies in Klinefelter's syndrome.
Horm Res. 2007;68(3):150-5. doi: 10.1159/000106375. Epub 2007 Jul 19.
Horm Res. 2007.
PMID: 17641549
Review.
Consensus statement on iodine deficiency disorders in Hong Kong.
But B, Chan CW, Chan F, Chan KW, Cheng AW, Cheung P, Choi KL, Chow CB, Chow FC, Eastman C, Fok TF, Fung LM, Gomes C, Huen KF, Ip TP, Kung AW, Lam KS, Lam YY, Lao T, Lee CY, Lee KF, Leung J, Leung NK, Li D, Li J, Lo KW, Lo L, Ng KL, Siu SC, Tam S, Tan KC, Tiu SC, Tse HY, Tse W, Wong G, Wong S, Wong W, Yeung VT, Young R, Yu CM, Yu R; Expert Panel Group On Iodine Deficiency Disorders In Hong Kong.
But B, et al.
Hong Kong Med J. 2003 Dec;9(6):446-53.
Hong Kong Med J. 2003.
PMID: 14660812
Free article.
Review.
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DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Lam CW, Li CK, Lai CK, Tong SF, Chan KY, Ng GS, Yuen YP, Cheng AW, Chan YW.
Lam CW, et al.
Mol Genet Metab. 2002 Jan;75(1):91-5. doi: 10.1006/mgme.2001.3267.
Mol Genet Metab. 2002.
PMID: 11825068
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Novel donor splice site mutation of ABCG5 gene in sitosterolemia.
Lam CW, Cheng AW, Tong SF, Chan YW.
Lam CW, et al.
Mol Genet Metab. 2002 Feb;75(2):178-80. doi: 10.1006/mgme.2001.3285.
Mol Genet Metab. 2002.
PMID: 11855938
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Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia.
Lam CW, Cheng AW, Poon WT, Yuen YP, Huen KF.
Lam CW, et al.
Clin Chim Acta. 2006 Dec;374(1-2):151-2. doi: 10.1016/j.cca.2006.03.021. Epub 2006 May 15.
Clin Chim Acta. 2006.
PMID: 16698006
No abstract available.
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