Lee CC - 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: lee 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

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: lee cc. Prenat Diagn. 2002 Dec;22(12):1063-6. doi: 10.1002/pd.459. Prenat Diagn. 2002. PMID: 12454959

3

Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly.

Chen CP, Tzen CY, Chang TY, Lin CJ, Wang W, Lee CC, Town DD, Chen LF, Lee MS. Chen CP, et al. Among authors: lee ms, lee cc. Prenat Diagn. 2002 Dec;22(12):1112-3. doi: 10.1002/pd.471. Prenat Diagn. 2002. PMID: 12454968 No abstract available.

4

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.

Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS. Chen CP, et al. Among authors: lee cc. Prenat Diagn. 2003 Jan;23(1):40-3. doi: 10.1002/pd.517. Prenat Diagn. 2003. PMID: 12533811

5

Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.

Chen CP, Hwu YM, Yeh LF, Chern SR, Lee CC, Wang W. Chen CP, et al. Among authors: lee cc. Fertil Steril. 2003 May;79(5):1231-3. doi: 10.1016/s0015-0282(03)00161-4. Fertil Steril. 2003. PMID: 12738525 Free article.

6

Prenatal diagnosis of de novo terminal deletion of chromosome 7q.

Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Lee MS, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Prenat Diagn. 2003 May;23(5):375-9. doi: 10.1002/pd.602. Prenat Diagn. 2003. PMID: 12749033

7

Second-trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1-->qter.

Chen CP, Chang TY, Tzen CY, Wang W, Lee CC, Chen LF, Lee MS, Lin SP. Chen CP, et al. Among authors: lee ms, lee cc. Ultrasound Obstet Gynecol. 2003 May;21(5):516-8. doi: 10.1002/uog.79. Ultrasound Obstet Gynecol. 2003. PMID: 12768570 Free article. 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: lee cc. 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: lee cc. Prenat Diagn. 2003 Jun;23(6):519-20. doi: 10.1002/pd.622. Prenat Diagn. 2003. PMID: 12813773 No abstract available.

10

Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.

Chen CP, Chern SR, Lee CC, Chen LF, Chin DT, Tzen CY, Wang W. Chen CP, et al. Among authors: lee cc. Prenat Diagn. 2003 Sep;23(9):758-61. doi: 10.1002/pd.684. Prenat Diagn. 2003. PMID: 12975789

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