Limwongse C - Search Results

1

Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis.

Schrijver I, Karnsakul W, Limwongse C, Ramalingam S, Sankaran R, Gardner P, Moss R. Schrijver I, et al. Among authors: limwongse c. Am J Med Genet A. 2005 Feb 15;133A(1):103-5. doi: 10.1002/ajmg.a.30472. Am J Med Genet A. 2005. PMID: 15744829 No abstract available.

2

Six novel ATP7B mutations in Thai patients with Wilson disease.

Panichareon B, Taweechue K, Thongnoppakhun W, Aksornworanart M, Pithukpakorn M, Yenchitsomanus PT, Limwongse C, Limjindaporn T. Panichareon B, et al. Among authors: limwongse c. Eur J Med Genet. 2011 Mar-Apr;54(2):103-7. doi: 10.1016/j.ejmg.2010.10.008. Epub 2010 Oct 27. Eur J Med Genet. 2011. PMID: 21034864

3

An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of the RMRP gene associated with chondrodysplasia and severe immunodeficiency.

Vatanavicharn N, Visitsunthorn N, Pho-iam T, Jirapongsananuruk O, Pacharn P, Chokephaibulkit K, Limwongse C, Wasant P. Vatanavicharn N, et al. Among authors: limwongse c. J Appl Genet. 2010;51(4):523-8. doi: 10.1007/BF03208884. J Appl Genet. 2010. PMID: 21063072

4

Mutations of the FLT3 gene in adult acute myeloid leukemia: determination of incidence and identification of a novel mutation in a Thai population.

Auewarakul CU, Sritana N, Limwongse C, Thongnoppakhun W, Yenchitsomanus PT. Auewarakul CU, et al. Among authors: limwongse c. Cancer Genet Cytogenet. 2005 Oct 15;162(2):127-34. doi: 10.1016/j.cancergencyto.2005.03.011. Cancer Genet Cytogenet. 2005. PMID: 16213360

5

Novel and de-novo truncating PAX6 mutations and ocular phenotypes in Thai aniridia patients.

Atchaneeyasakul LO, Trinavarat A, Dulayajinda D, Kumpornsin K, Thongnoppakhun W, Yenchitsomanus PT, Limwongse C. Atchaneeyasakul LO, et al. Among authors: limwongse c. Ophthalmic Genet. 2006 Mar;27(1):21-7. doi: 10.1080/13816810500481667. Ophthalmic Genet. 2006. PMID: 16543198

6

Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP).

Thongnoppakhun W, Limwongse C, Vareesangthip K, Sirinavin C, Bunditworapoom D, Rungroj N, Yenchitsomanus PT. Thongnoppakhun W, et al. Among authors: limwongse c. BMC Med Genet. 2004 Feb 3;5:2. doi: 10.1186/1471-2350-5-2. BMC Med Genet. 2004. PMID: 15018634 Free PMC article.

7

High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.

Wattanasirichaigoon D, Limwongse C, Jariengprasert C, Yenchitsomanus PT, Tocharoenthanaphol C, Thongnoppakhun W, Thawil C, Charoenpipop D, Pho-iam T, Thongpradit S, Duggal P. Wattanasirichaigoon D, et al. Among authors: limwongse c. Clin Genet. 2004 Nov;66(5):452-60. doi: 10.1111/j.1399-0004.2004.00325.x. Clin Genet. 2004. PMID: 15479191

8

A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 gene.

Pho-Iam T, Thongnoppakhun W, Yenchitsomanus PT, Limwongse C. Pho-Iam T, et al. Among authors: limwongse c. World J Gastroenterol. 2005 Mar 21;11(11):1634-8. doi: 10.3748/wjg.v11.i11.1634. World J Gastroenterol. 2005. PMID: 15786540 Free PMC article.

9

Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian population.

Auewarakul CU, Leecharendkeat A, Thongnoppakhun W, Limwongse C, Tocharoentanaphol C. Auewarakul CU, et al. Among authors: limwongse c. Haematologica. 2006 May;91(5):675-8. Epub 2006 Apr 19. Haematologica. 2006. PMID: 16627249

10

Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.

Atchaneeyasakul LO, Jinda W, Sakolsatayadorn N, Trinavarat A, Ruangvoravate N, Thanasombatskul N, Thongnoppakhun W, Limwongse C. Atchaneeyasakul LO, et al. Among authors: limwongse c. Ophthalmic Genet. 2008 Sep;29(3):139-44. doi: 10.1080/13816810802087394. Ophthalmic Genet. 2008. PMID: 18766995

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