Lin SP - Search Results

1

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.

Chen CP, Lin SP, Lin CC, Chen YJ, Chern SR, Li YC, Hsieh LJ, Lee CC, Pan CW, Wang W. Chen CP, et al. Among authors: lin sp, lin cc. Am J Med Genet A. 2006 Jul 15;140(14):1594-600. doi: 10.1002/ajmg.a.31329. Am J Med Genet A. 2006. PMID: 16770806 Review.

2

Fetal cervico-mediastinal cystic hygroma associated with maternal serum screening positive for Down syndrome.

Chen CP, Sheu JC, Wang W, Lin SP, Chang TY, Tzen CY. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2002 Feb;22(2):166. doi: 10.1002/pd.276. Prenat Diagn. 2002. PMID: 11857633 No abstract available.

3

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.

4

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.

5

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

6

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

7

Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis.

Chen CP, Chern SR, Lin SP, Wang W, Tsai FJ. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2003 Feb;23(2):175-6. doi: 10.1002/pd.523. Prenat Diagn. 2003. PMID: 12575031 No abstract available.

8

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

9

Association of partial trisomy 9 (9pter-->q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly.

Chen CP, Hsu CH, Lin SP, Ho CS, Lee CC, Wang W. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2003 Jun;23(6):519-20. doi: 10.1002/pd.622. Prenat Diagn. 2003. PMID: 12813773 No abstract available.

10

Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II.

Chen CP, Lin SP, Tzen CY, Tsai FJ, Hwu WL, Wang W. Chen CP, et al. Among authors: lin sp. Prenat Diagn. 2004 Mar;24(3):231-2. doi: 10.1002/pd.807. Prenat Diagn. 2004. PMID: 15057961 No abstract available.

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