Chen CP - Search Results

1

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.

Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W. Chen CP, et al. Among authors: chen yj, chen m. Prenat Diagn. 2006 Aug;26(8):725-9. doi: 10.1002/pd.1496. Prenat Diagn. 2006. PMID: 16927391

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. Prenat Diagn. 2002 Jan;22(1):5-7. doi: 10.1002/pd.202. Prenat Diagn. 2002. PMID: 11810641

3

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. Prenat Diagn. 2002 Feb;22(2):166. doi: 10.1002/pd.276. Prenat Diagn. 2002. PMID: 11857633 No abstract available.

4

Sonographic appearance of the uterus after simple square suturing for rapid control of postpartum hemorrhage and preservation of fertility.

Chen CP, Chang TY, Yeh LF, Lin CJ, Wang W. Chen CP, et al. J Clin Ultrasound. 2002 Mar-Apr;30(3):189-91. doi: 10.1002/jcu.10046. J Clin Ultrasound. 2002. PMID: 11948577

5

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. Fertil Steril. 2002 Jun;77(6):1285-7. doi: 10.1016/s0015-0282(02)03118-7. Fertil Steril. 2002. PMID: 12057743 Free article.

6

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. Prenat Diagn. 2002 Jul;22(7):634-6. doi: 10.1002/pd.357. Prenat Diagn. 2002. PMID: 12124705 No abstract available.

7

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. Prenat Diagn. 2002 Aug;22(8):736-7. doi: 10.1002/pd.377. Prenat Diagn. 2002. PMID: 12210587 No abstract available.

8

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. Prenat Diagn. 2002 Oct;22(10):887-92. doi: 10.1002/pd.433. Prenat Diagn. 2002. PMID: 12378571

9

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

10

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: chen lf. Prenat Diagn. 2002 Dec;22(12):1112-3. doi: 10.1002/pd.471. Prenat Diagn. 2002. PMID: 12454968 No abstract available.

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