Lin SP - Search Results

1

Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR.

Hung CC, Lin SY, Lin SP, Niu DM, Lee NC, Cheng WF, Chen CP, Lin WL, Lee CN, Su YN. Hung CC, et al. Among authors: lin sy, lin wl, lin sp. Electrophoresis. 2009 Jan;30(2):410-6. doi: 10.1002/elps.200800225. Electrophoresis. 2009. PMID: 19137525

2

Bilateral calcified ovarian fibromas in a patient with Sotos syndrome.

Chen CP, Yang YC, Lin SP, Wang W, Chang CL, Chang KM. Chen CP, et al. Among authors: lin sp. Fertil Steril. 2002 Jun;77(6):1285-7. doi: 10.1016/s0015-0282(02)03118-7. Fertil Steril. 2002. PMID: 12057743 Free article.

3

Microcephaly with dysgenesis of corpus callosum and colpocephaly in the survivor after the first-trimester death of a monochorionic co-twin.

Chen CP, Lin SP, Chiu NC. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2002 Jul;22(7):634-6. doi: 10.1002/pd.357. Prenat Diagn. 2002. PMID: 12124705 No abstract available.

4

Perinatal imaging findings of inherited Sotos syndrome.

Chen CP, Lin SP, Chang TY, Chiu NC, Shih SL, Lin CJ, Wang W, Hsu HC. Chen CP, et al. Among authors: lin cj, lin sp. Prenat Diagn. 2002 Oct;22(10):887-92. doi: 10.1002/pd.433. Prenat Diagn. 2002. PMID: 12378571

5

Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.

Chen CP, Chang TY, Shih JC, Lin SP, Lin CJ, Wang W, Lee CC, Town DD, Pan CW, Tzen CY. Chen CP, et al. Among authors: lin cj, lin sp. Prenat Diagn. 2002 Dec;22(12):1063-6. doi: 10.1002/pd.459. Prenat Diagn. 2002. PMID: 12454959

6

Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.

Chen CP, Lin SP, Chern SR, Shih SL, Lee CC, Wang W, Liao YW. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2003 Jun;23(6):504-8. doi: 10.1002/pd.629. Prenat Diagn. 2003. PMID: 12813767

7

Detection of chromosome aberrations during prenatal genetic testing for single gene disorders.

Chen CP, Lin SP. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2004 Nov;24(11):924-5. doi: 10.1002/pd.953. Prenat Diagn. 2004. PMID: 15565556 No abstract available.

8

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W. Chen CP, et al. Among authors: lin sp, lin cc. Prenat Diagn. 2005 Feb;25(2):112-8. doi: 10.1002/pd.1083. Prenat Diagn. 2005. PMID: 15712324 Review.

9

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.

Chen CP, Chern SR, Sheu JC, Lin SP, Hsu CY, Chang TY, Lee CC, Wang W, Chen HE. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2005 Jun;25(6):502-6. doi: 10.1002/pd.1181. Prenat Diagn. 2005. PMID: 15966046

10

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.

Chen CP, Chern SR, Lin SP, Lin CC, Li YC, Wang TH, Lee CC, Pan CW, Hsieh LJ, Wang W. Chen CP, et al. Among authors: lin sp, lin cc. Am J Med Genet A. 2005 Dec 1;139A(2):146-50. doi: 10.1002/ajmg.a.30997. Am J Med Genet A. 2005. PMID: 16278896

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