Chen M - Search Results

1

Polyhydramnios as a sole ultrasonographic finding for detecting fetal hemolytic anemia caused by anti-c alloimmunization.

Wang SC, Wu YC, Wu WJ, Lee MH, Lin WH, Ma GC, Chen M. Wang SC, et al. Among authors: chen m. Taiwan J Obstet Gynecol. 2022 Jul;61(4):722-725. doi: 10.1016/j.tjog.2022.04.006. Taiwan J Obstet Gynecol. 2022. PMID: 35779930 Free article.

2

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.

3

Balloon pulmonary valvuloplasty for valvular pulmonary stenosis in double outlet right ventricle incriminating 46,X,der(X)t(X;3)(q28;q13.2)mat in an infant.

Lee ML, Chen M, Lee MH. Lee ML, et al. Among authors: chen m. Int J Cardiol. 2007 Jan 2;114(1):e27-30. doi: 10.1016/j.ijcard.2006.07.210. Epub 2006 Oct 30. Int J Cardiol. 2007. PMID: 17074406 No abstract available.

4

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.

5

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

6

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.

7

First prenatal exclusion of cystic fibrosis in East Asia.

Wong LJ, Lee MH, Chen M, Alper OM, Tsao LY, Wang BT. Wong LJ, et al. Among authors: chen m. Pediatr Int. 2007 Oct;49(5):686-7. doi: 10.1111/j.1442-200X.2007.02437.x. Pediatr Int. 2007. PMID: 17875103 No abstract available.

8

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.

9

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

10

A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPSTE24 gene.

Chen M, Kuo HH, Huang YC, Ke YY, Chang SP, Chen CP, Lee DJ, Lee ML, Lee MH, Chen TH, Chen CH, Lin HM, Liu CS, Ma GC. Chen M, et al. Among authors: chen th, chen ch, chen cp. Am J Med Genet A. 2009 Jul;149A(7):1550-4. doi: 10.1002/ajmg.a.32768. Am J Med Genet A. 2009. PMID: 19504603 No abstract available.

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