Wang W - Search Results

1

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.

Chen CP, Chen M, Wu CH, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen LF, Wang W. Chen CP, et al. Among authors: wang w. Taiwan J Obstet Gynecol. 2017 Aug;56(4):554-557. doi: 10.1016/j.tjog.2017.06.004. Taiwan J Obstet Gynecol. 2017. PMID: 28805618 Free article. Review.

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

3

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. Among authors: wang w. J Clin Ultrasound. 2002 Mar-Apr;30(3):189-91. doi: 10.1002/jcu.10046. J Clin Ultrasound. 2002. PMID: 11948577

4

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

5

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

6

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

7

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

8

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

9

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: wang w. Prenat Diagn. 2003 Jan;23(1):40-3. doi: 10.1002/pd.517. Prenat Diagn. 2003. PMID: 12533811

10

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

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