Chen M - Search Results

1

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.

Chen CP, Chen M, Su YN, Tsai FJ, Chern SR, Hsu CY, Wu PC, Town DD, Lee DJ, Ma GC, Wang W. Chen CP, et al. Among authors: chen m. Taiwan J Obstet Gynecol. 2010 Sep;49(3):320-6. doi: 10.1016/S1028-4559(10)60068-X. Taiwan J Obstet Gynecol. 2010. PMID: 21056318 Free article.

2

Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.

Chen M, Yeh GP, Shih JC, Wang BT. Chen M, et al. Prenat Diagn. 2004 Feb;24(2):137-43. doi: 10.1002/pd.814. Prenat Diagn. 2004. PMID: 14974123 Review.

3

Antenatal treatment of chylothorax and cystic hygroma with OK-432 in nonimmune hydrops fetalis.

Chen M, Chen CP, Shih JC, Chou HC, Yu CL, Wang BT, Hsieh CY. Chen M, et al. Among authors: chen cp. Fetal Diagn Ther. 2005 Jul-Aug;20(4):309-15. doi: 10.1159/000085092. Fetal Diagn Ther. 2005. PMID: 15980647

4

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.

Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W. Chen CP, et al. Among authors: chen yj, chen m. Prenat Diagn. 2006 Aug;26(8):725-9. doi: 10.1002/pd.1496. Prenat Diagn. 2006. PMID: 16927391

5

Prenatal sonographic features of hypospadia: two- and three-dimensional findings.

Fang KH, Wu JL, Chen M, Yeh GP, Chou PH, Hsu JC, Hsieh CT. Fang KH, et al. Among authors: chen m. Taiwan J Obstet Gynecol. 2006 Mar;45(1):53-5. doi: 10.1016/S1028-4559(09)60191-1. Taiwan J Obstet Gynecol. 2006. PMID: 17272209 Free article.

6

Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax.

Chen M, Hsieh CY, Shih JC, Chou CH, Ma GC, Chen TH, Lee TH, Tsai HD, Cameron AD, Chen CP. Chen M, et al. Among authors: chen th, chen cp. Prenat Diagn. 2007 May;27(5):435-41. doi: 10.1002/pd.1704. Prenat Diagn. 2007. PMID: 17295350

7

Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients.

Kuo SJ, Wang BB, Chang CS, Chen TH, Yeh KT, Lee DJ, Yin PL, Chen M. Kuo SJ, et al. Among authors: chen m, chen th. Taiwan J Obstet Gynecol. 2007 Jun;46(2):146-51. doi: 10.1016/S1028-4559(07)60008-4. Taiwan J Obstet Gynecol. 2007. PMID: 17638622 Free article.

8

Interstitial deletion 13q31 associated with normal phenotype: cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion.

Ke YY, Lee DJ, Ma GC, Lee MH, Wang BT, Chen M. Ke YY, et al. Among authors: chen m. J Formos Med Assoc. 2007 Jul;106(7):582-8. doi: 10.1016/S0929-6646(07)60010-2. J Formos Med Assoc. 2007. PMID: 17660149 Free article.

9

Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography.

Ma GC, Chang SD, Chang Y, Chang SP, Yang CW, Lee MJ, Lee TH, Chen M. Ma GC, et al. Among authors: chen m. Fertil Steril. 2008 Oct;90(4):1279-82. doi: 10.1016/j.fertnstert.2007.10.075. Epub 2008 Feb 4. Fertil Steril. 2008. PMID: 18249379 Free article.

10

A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy.

Ma GC, Liu CS, Chang SP, Yeh KT, Ke YY, Chen TH, Wang BB, Kuo SJ, Shih JC, Chen M. Ma GC, et al. Among authors: chen m, chen th. Prenat Diagn. 2008 Nov;28(11):1057-63. doi: 10.1002/pd.2130. Prenat Diagn. 2008. PMID: 18973153

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