Chen M - Search Results

1

Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding.

Lee NC, Chang SP, Chang CS, Chen CH, Lee DJ, Lin CC, Hwu WL, Chen M. Lee NC, et al. Among authors: chen m, chen ch. Prenat Diagn. 2009 Nov;29(11):1058-60. doi: 10.1002/pd.2332. Prenat Diagn. 2009. PMID: 19629965 No abstract available.

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

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

Huge duplication cyst of small intestine: ultrasonographic features and prenatal aspiration.

Chen M, Ho WK, Hsieh TC, Lee CS, Hsiao CC, Chang SP, Lee DJ, Yang AD. Chen M, et al. Prenat Diagn. 2006 Jan;26(1):86-8. doi: 10.1002/pd.1324. Prenat Diagn. 2006. PMID: 16374896 No abstract available.

5

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

6

Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies.

Chen M, Chang SP, Yin PL, Sapeta M, Barringer S, Kuo SJ, Yu HT, Wang BB. Chen M, et al. Prenat Diagn. 2006 Apr;26(4):383-7. doi: 10.1002/pd.1414. Prenat Diagn. 2006. PMID: 16566043 No abstract available.

7

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

8

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.

9

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.

10

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.

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