Chang SP - Search Results

1

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: chang sd, chang y, chang sp. 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.

2

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: chang yy, chang sp. Prenat Diagn. 2006 Mar;26(3):226-30. doi: 10.1002/pd.1385. Prenat Diagn. 2006. PMID: 16475235

3

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: chang sp. Prenat Diagn. 2008 Nov;28(11):1057-63. doi: 10.1002/pd.2130. Prenat Diagn. 2008. PMID: 18973153

4

Phenotype and genotype of two Taiwanese cystic fibrosis siblings and a survey of delta F508 in East Asians.

Lin CJ, Chang SP, Ke YY, Chiu HY, Tsao LY, Chen M. Lin CJ, et al. Among authors: chang sp. Pediatr Neonatol. 2008 Dec;49(6):240-4. doi: 10.1016/S1875-9572(09)60018-8. Pediatr Neonatol. 2008. PMID: 19166122 Free article.

5

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: chang sp. 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.

6

Differential expression of NUDT9 at different phases of the menstrual cycle and in different components of normal and neoplastic human endometrium.

Chen LY, Chen TH, Wen PY, Chou CH, Ying TH, Chang SP, Ma GC, Chen M. Chen LY, et al. Among authors: chang sp. Taiwan J Obstet Gynecol. 2009 Jun;48(2):96-107. doi: 10.1016/S1028-4559(09)60266-7. Taiwan J Obstet Gynecol. 2009. PMID: 19574167 Free article.

7

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: chang cs, chang sp. Prenat Diagn. 2009 Nov;29(11):1058-60. doi: 10.1002/pd.2332. Prenat Diagn. 2009. PMID: 19629965 No abstract available.

8

Number of somatic mutations in the mitochondrial D-loop region indicates poor prognosis in breast cancer, independent of TP53 mutation.

Kuo SJ, Chen M, Ma GC, Chen ST, Chang SP, Lin WY, Chen YC, Lee TH, Lin TT, Liu CS. Kuo SJ, et al. Among authors: chang sp. Cancer Genet Cytogenet. 2010 Sep;201(2):94-101. doi: 10.1016/j.cancergencyto.2010.05.013. Cancer Genet Cytogenet. 2010. PMID: 20682393

9

A compound heterozygous GNPTAB mutation causes mucolipidosis II with marked hair color change in a Han Chinese baby.

Ma GC, Ke YY, Chang SP, Lee DJ, Chen M. Ma GC, et al. Among authors: chang sp. Am J Med Genet A. 2011 Apr;155A(4):931-4. doi: 10.1002/ajmg.a.33834. Epub 2011 Mar 17. Am J Med Genet A. 2011. PMID: 21416587 No abstract available.

10

Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.

Chen CP, Chen M, Ma GC, Chang SP, Chen YY, Wu PC, Chen LF, Wang W. Chen CP, et al. Among authors: chang sp. Taiwan J Obstet Gynecol. 2011 Jun;50(2):253-7. doi: 10.1016/j.tjog.2011.04.007. Taiwan J Obstet Gynecol. 2011. PMID: 21791323 Free article. No abstract available.

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