Wang CH - Search Results

1

Molecular aspects of Dravet syndrome patients in Taiwan.

Lin WD, Chang KP, Wang CH, Chen SJ, Fan PC, Weng WC, Lin WC, Tsai Y, Tsai CH, Chou IC, Tsai FJ. Lin WD, et al. Among authors: wang ch. Clin Chim Acta. 2013 Jun 5;421:34-40. doi: 10.1016/j.cca.2013.02.015. Epub 2013 Feb 26. Clin Chim Acta. 2013. PMID: 23485646

2

A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda.

Shi YR, Lee CC, Hsu YA, Wang CH, Tsai FJ. Shi YR, et al. Among authors: wang ch. Hum Hered. 2002;54(1):54-6. doi: 10.1159/000066694. Hum Hered. 2002. PMID: 12446987

3

Genetic and biochemical study in a patient with glutaric acidemia type I.

Lin WD, Wang CH, Lai CC, Lee CC, Tsai FJ. Lin WD, et al. Among authors: wang ch. J Formos Med Assoc. 2004 Jul;103(7):549-54. J Formos Med Assoc. 2004. PMID: 15318278

4

Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patients.

Wang CH, Wu KH, Tsai FJ, Peng CT, Tsai CH. Wang CH, et al. Hemoglobin. 2006;30(2):257-62. doi: 10.1080/03630260600642609. Hemoglobin. 2006. PMID: 16798651 Clinical Trial.

5

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ. Lin CC, et al. Among authors: wang ch. Prenat Diagn. 2006 Oct;26(10):898-902. doi: 10.1002/pd.1520. Prenat Diagn. 2006. PMID: 16915592

6

Greig cephalopolysyndactyly syndrome in a family.

Wang CH, Tsai FJ, Shi YR. Wang CH, et al. Acta Paediatr Taiwan. 2006 Mar-Apr;47(2):95-9. Acta Paediatr Taiwan. 2006. PMID: 16927636

7

Genetic mutation profile of isovaleric acidemia patients in Taiwan.

Lin WD, Wang CH, Lee CC, Lai CC, Tsai Y, Tsai FJ. Lin WD, et al. Among authors: wang ch. Mol Genet Metab. 2007 Feb;90(2):134-9. doi: 10.1016/j.ymgme.2006.08.011. Epub 2006 Oct 4. Mol Genet Metab. 2007. PMID: 17027310

8

Penile length of normal boys in Taiwan.

Wang CH, Lin WD, Bau DT, Tsai CH, Liu DC, Tsai FJ. Wang CH, et al. Acta Paediatr Taiwan. 2006 Nov-Dec;47(6):293-6. Acta Paediatr Taiwan. 2006. PMID: 17407980

9

Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients.

Lin WD, Lin SP, Wang CH, Hwu WL, Chuang CK, Lin SJ, Tsai Y, Chen CP, Tsai FJ. Lin WD, et al. Among authors: wang ch. Clin Chim Acta. 2008 Aug;394(1-2):89-93. doi: 10.1016/j.cca.2008.04.014. Epub 2008 Apr 27. Clin Chim Acta. 2008. PMID: 18486607

10

Molecular analysis of Taiwanese patients with 3-hydroxy-3-methylglutaryl CoA lyase deficiency.

Lin WD, Wang CH, Lai CC, Tsai Y, Wu JY, Chen CP, Tsai FJ. Lin WD, et al. Among authors: wang ch. Clin Chim Acta. 2009 Mar;401(1-2):33-6. doi: 10.1016/j.cca.2008.11.004. Epub 2008 Nov 12. Clin Chim Acta. 2009. PMID: 19036343

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

4,826 results

Search Page