Chen M - Search Results

1

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.

2

Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities.

Chen M, Shih JC, Wang BT. Chen M, et al. Prenat Diagn. 2003 Dec 30;23(13):1102-3. doi: 10.1002/pd.765. Prenat Diagn. 2003. PMID: 14692004 No abstract available.

3

Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.

Hsieh LJ, Hsieh TC, Yeh GP, Lin MI, Chen M, Wang BB. Hsieh LJ, et al. Among authors: chen m. Fetal Diagn Ther. 2004 Jul-Aug;19(4):356-60. doi: 10.1159/000077965. Fetal Diagn Ther. 2004. PMID: 15192296

4

Meconium peritonitis presenting as isolated massive fetal ascites.

Chen FY, Chen M, Shih JC, Tsao PN, Lee CN, Hsieh FJ. Chen FY, et al. Among authors: chen m. Prenat Diagn. 2004 Nov;24(11):930-1. doi: 10.1002/pd.999. Prenat Diagn. 2004. PMID: 15565655 No abstract available.

5

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

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: chen th, chen wl. Prenat Diagn. 2006 Mar;26(3):226-30. doi: 10.1002/pd.1385. Prenat Diagn. 2006. PMID: 16475235

7

Persistent fifth aortic arch associated with 22q11.2 deletion syndrome.

Lee ML, Chen HN, Chen M, Tsao LY, Wang BT, Lee MH, Chiu IS. Lee ML, et al. Among authors: chen m, chen hn. J Formos Med Assoc. 2006 Apr;105(4):284-9. doi: 10.1016/S0929-6646(09)60119-4. J Formos Med Assoc. 2006. PMID: 16618608 Free article.

8

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

9

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.

10

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

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