Chern SR - Search Results

1

Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).

Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W. Chen CP, et al. Among authors: chern sr. Prenat Diagn. 2005 Dec;25(12):1170-2. doi: 10.1002/pd.1300. Prenat Diagn. 2005. PMID: 16315335 No abstract available.

2

Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis.

Chen CP, Chern SR, Du SH, Wang W. Chen CP, et al. Among authors: chern sr. Prenat Diagn. 2002 Jan;22(1):5-7. doi: 10.1002/pd.202. Prenat Diagn. 2002. PMID: 11810641

3

Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.

Chen CP, Chern SR, Chang TY, Lin CJ, Wang W, Tzen CY. Chen CP, et al. Among authors: chern sr. Prenat Diagn. 2002 Aug;22(8):736-7. doi: 10.1002/pd.377. Prenat Diagn. 2002. PMID: 12210587 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: chern sr. Prenat Diagn. 2003 Jan;23(1):40-3. doi: 10.1002/pd.517. Prenat Diagn. 2003. PMID: 12533811

5

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: chern sr. Prenat Diagn. 2003 Feb;23(2):175-6. doi: 10.1002/pd.523. Prenat Diagn. 2003. PMID: 12575031 No abstract available.

6

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: chern sr. Prenat Diagn. 2003 Apr;23(4):352-3. doi: 10.1002/pd.573. Prenat Diagn. 2003. PMID: 12673645 No abstract available.

7

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: chern sr. Fertil Steril. 2003 May;79(5):1231-3. doi: 10.1016/s0015-0282(03)00161-4. Fertil Steril. 2003. PMID: 12738525 Free article.

8

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: chern sr. Prenat Diagn. 2003 May;23(5):375-9. doi: 10.1002/pd.602. Prenat Diagn. 2003. PMID: 12749033

9

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: chern sr. Prenat Diagn. 2003 Jun;23(6):504-8. doi: 10.1002/pd.629. Prenat Diagn. 2003. PMID: 12813767

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: chern sr. Prenat Diagn. 2003 Sep;23(9):758-61. doi: 10.1002/pd.684. Prenat Diagn. 2003. PMID: 12975789

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