Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

481 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Prenatal diagnosis of Jacobsen syndrome associated with a distal 11q deletion and a distal 8q duplication by chromosome microarray analysis in a fetus with a de novo unbalanced translocation of 46,XX,der(11)t(8;11)(q24.13;q23.3) and multiple congenital anomalies on fetal ultrasound.
Chen CP, Huang JP, Wu FT, Wu PS, Pan YT, Lee CC, Chen WL, Wang W. Chen CP, et al. Among authors: wu ps. Taiwan J Obstet Gynecol. 2024 Nov;63(6):922-926. doi: 10.1016/j.tjog.2024.09.012. Taiwan J Obstet Gynecol. 2024. PMID: 39482005 Free article.
Detection of chromosome 5q interstitial deletion of 5q14.3-q31.1 by chromosome microarray analysis in a second-trimester fetus with multiple congenital anomalies and a literature review of chromosome 5q interstitial deletion syndrome.
Chen CP, Huang JP, Wu FT, Wu PS, Pan YT, Wang W. Chen CP, et al. Among authors: wu ps. Taiwan J Obstet Gynecol. 2024 Nov;63(6):918-921. doi: 10.1016/j.tjog.2024.09.011. Taiwan J Obstet Gynecol. 2024. PMID: 39482004 Free article. Review.
Prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11)(p11.2p13)ins(11)(q21p11.2p13) and maternal intrachromosomal insertion of ins(11)(q21p11.2p13).
Chen CP, Chen CY, Wu FT, Wu PS, Pan YT, Lee CC, Chen WL, Wang W. Chen CP, et al. Among authors: wu ps. Taiwan J Obstet Gynecol. 2024 Nov;63(6):913-917. doi: 10.1016/j.tjog.2024.09.010. Taiwan J Obstet Gynecol. 2024. PMID: 39482003 Free article.
First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.2;q37.3)dmat.
Chen CP, Weng SL, Wu FT, Wu PS, Pan YT, Chen WL, Yang CW, Wang W. Chen CP, et al. Among authors: wu ps. Taiwan J Obstet Gynecol. 2024 Nov;63(6):909-912. doi: 10.1016/j.tjog.2024.09.009. Taiwan J Obstet Gynecol. 2024. PMID: 39482002 Free article.
Blood pressure targets, medication consideration and unique concerns in elderly hypertension IV: Focus on frailty, orthostatic hypotension, and resistant hypertension.
Wu PS, Chao CT, Hsiao CH, Yang CF, Lee YH, Lin HJ, Yeh CF, Lee LT, Huang KC, Lee MC, Huang CK, Lin YH, Chen MY, Chan DC. Wu PS, et al. J Formos Med Assoc. 2024 Oct 5:S0929-6646(24)00442-X. doi: 10.1016/j.jfma.2024.09.022. Online ahead of print. J Formos Med Assoc. 2024. PMID: 39370367 Free article. Review.
481 results