Lee MH - 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: lee mh. 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

Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction.

Kuo SJ, Ma GC, Chang SP, Wu HH, Chen CP, Chang TM, Lin WH, Wu SH, Lee MH, Hwu WL, Chen M. Kuo SJ, et al. Among authors: lee mh. Taiwan J Obstet Gynecol. 2011 Dec;50(4):468-73. doi: 10.1016/j.tjog.2011.10.012. Taiwan J Obstet Gynecol. 2011. PMID: 22212319 Free article.

3

A Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucleated Red Blood Cells.

Ma GC, Lin WH, Huang CE, Chang TY, Liu JY, Yang YJ, Lee MH, Wu WJ, Chang YS, Chen M. Ma GC, et al. Among authors: lee mh. Micromachines (Basel). 2019 Feb 17;10(2):132. doi: 10.3390/mi10020132. Micromachines (Basel). 2019. PMID: 30781548 Free PMC article.

4

Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to Trio Analyses.

Chen M, Wu WJ, Lee MH, Ku TH, Ma GC. Chen M, et al. Among authors: lee mh. Genes (Basel). 2020 Aug 22;11(9):979. doi: 10.3390/genes11090979. Genes (Basel). 2020. PMID: 32842633 Free PMC article.

5

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray.

Yao TY, Wu WJ, Law KS, Lee MH, Chang SP, Lee DJ, Lin WH, Chen M, Ma GC. Yao TY, et al. Among authors: lee dj, lee mh. Diagnostics (Basel). 2021 Aug 12;11(8):1457. doi: 10.3390/diagnostics11081457. Diagnostics (Basel). 2021. PMID: 34441391 Free PMC article.

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: lee dj, lee mh. 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

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: lee mh. 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

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: lee dj, lee mh, lee ml. 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.

9

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: lee mh. 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.

10

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: lee mh. 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.

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