Lee MS - Search Results

1

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.

2

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.

3

Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.

Chen CP, Chang TY, Chern SR, Town DD, Pan CW, Lee MS, Wang W. Chen CP, et al. Among authors: lee ms. Prenat Diagn. 2003 Apr;23(4):352-3. doi: 10.1002/pd.573. Prenat Diagn. 2003. PMID: 12673645 No abstract available.

4

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

5

Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.

Chen CP, Chern SR, Hsu CY, Lee CC, Lee MS, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Prenat Diagn. 2005 Apr;25(4):334-6. doi: 10.1002/pd.1126. Prenat Diagn. 2005. PMID: 15849788 No abstract available.

6

Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.

Chen CP, Chang TY, Chern SR, Lee CC, Town DD, Lee MS, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Prenat Diagn. 2007 Apr;27(4):383-5. doi: 10.1002/pd.1678. Prenat Diagn. 2007. PMID: 17393556 No abstract available.

7

Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).

Chen CP, Chen YJ, Chern SR, Tsai FJ, Chang TY, Lee CC, Town DD, Lee MS, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Prenat Diagn. 2008 May;28(5):450-3. doi: 10.1002/pd.1993. Prenat Diagn. 2008. PMID: 18395879 No abstract available.

8

A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.

Chen CP, Tzen CY, Chern SR, Tsai FJ, Hsu CY, Lee CC, Lee MS, Pan CW, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Eur J Med Genet. 2009 Jan-Feb;52(1):59-61. doi: 10.1016/j.ejmg.2008.11.003. Epub 2008 Nov 19. Eur J Med Genet. 2009. PMID: 19049908

9

Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.

Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W. Chen CP, et al. Among authors: lee ms, lee cc. Taiwan J Obstet Gynecol. 2009 Dec;48(4):389-99. doi: 10.1016/S1028-4559(09)60329-6. Taiwan J Obstet Gynecol. 2009. PMID: 20045761 Free article.

10

Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes.

Chen CP, Su YN, Tsai FJ, Lin HH, Chern SR, Lee MS, Hwang JK, Chen TH, Wang W. Chen CP, et al. Among authors: lee ms. Taiwan J Obstet Gynecol. 2009 Dec;48(4):441-5. doi: 10.1016/S1028-4559(09)60343-0. Taiwan J Obstet Gynecol. 2009. PMID: 20045775 Free article. No abstract available.

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