Ko TM - Search Results

1

Thirteen X-chromosomal short tandem repeat loci multiplex data from Taiwanese.

Hwa HL, Chang YY, Lee JC, Yin HY, Chen YH, Tseng LH, Su YN, Ko TM. Hwa HL, et al. Among authors: ko tm. Int J Legal Med. 2009 May;123(3):263-9. doi: 10.1007/s00414-008-0310-y. Epub 2009 Jan 9. Int J Legal Med. 2009. PMID: 19132382

2

Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness.

Hwa HL, Ko TM, Hsu CJ, Huang CH, Chiang YL, Oong JL, Chen CC, Hsu CK. Hwa HL, et al. Among authors: ko tm. Genet Med. 2003 May-Jun;5(3):161-5. doi: 10.1097/01.GIM.0000066796.11916.94. Genet Med. 2003. PMID: 12792423

3

Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.

Hwa HL, Ko TM, Chang YY, Huang CH, Su YN, Tseng LH, Hsieh FJ. Hwa HL, et al. Among authors: ko tm. Prenat Diagn. 2004 Feb;24(2):121-4. doi: 10.1002/pd.817. Prenat Diagn. 2004. PMID: 14974120

4

Fetal gender determination using real-time quantitative polymerase chain reaction analysis of maternal plasma.

Hwa HL, Ko TM, Yen ML, Chiang YL. Hwa HL, et al. Among authors: ko tm. J Formos Med Assoc. 2004 May;103(5):364-8. J Formos Med Assoc. 2004. PMID: 15216403

5

Evaluation of second trimester maternal serum screening for Down's Syndrome using the Spiegelhalter-Knill-Jones (S-KJ) approach.

Hwa HL, Yen MF, Hsieh FJ, Ko TM, Chen TH. Hwa HL, et al. Among authors: ko tm. J Perinat Med. 2004;32(5):407-12. doi: 10.1515/JPM.2004.137. J Perinat Med. 2004. PMID: 15493716

6

A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease.

Chen M, Kuo SJ, Liu CS, Chen WL, Ko TM, Chen TH, Chang SP, Huang CH, Chang YY, Wang BT. Chen M, et al. Among authors: ko tm. Prenat Diagn. 2006 Mar;26(3):226-30. doi: 10.1002/pd.1385. Prenat Diagn. 2006. PMID: 16475235

7

Prenatal diagnosis and genetic analysis of a fetus with 47,XX,+21/46,XX mosaicism and XX/XY chimerism.

Hwa HL, Ko TM, Huang CH, Chang LS. Hwa HL, et al. Among authors: ko tm. J Formos Med Assoc. 2006 Aug;105(8):659-63. doi: 10.1016/S0929-6646(09)60165-0. J Formos Med Assoc. 2006. PMID: 16935767 Free article.

8

Risk prediction for Down's syndrome in young pregnant women using maternal serum biomarkers: determination of cut-off risk from receiver operating characteristic curve analysis.

Hwa HL, Ko TM, Hsieh FJ, Yen MF, Chou KP, Chen TH. Hwa HL, et al. Among authors: ko tm. J Eval Clin Pract. 2007 Apr;13(2):254-8. doi: 10.1111/j.1365-2753.2006.00687.x. J Eval Clin Pract. 2007. PMID: 17378872

9

Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification.

Huang CH, Chang YY, Chen CH, Kuo YS, Hwu WL, Gerdes T, Ko TM. Huang CH, et al. Among authors: ko tm. Genet Med. 2007 Apr;9(4):241-8. doi: 10.1097/gim.0b013e31803d35bc. Genet Med. 2007. PMID: 17438389 Free article.

10

Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.

Hwa HL, Chang YY, Chen CH, Kao YS, Jong YJ, Chao MC, Ko TM. Hwa HL, et al. Among authors: ko tm. J Formos Med Assoc. 2007 May;106(5):339-46. doi: 10.1016/S0929-6646(09)60318-1. J Formos Med Assoc. 2007. PMID: 17561468 Free article.

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