Kuo YL - Search Results

1

A de novo int22h-1/int22h-2-flanked Xq28 deletion-associated preferential X-inactivation in a female with severe hemophilia B.

Chen WC, Kao HJ, Kwok PY, Chiou SS, Kuo YL, Hsu WY, Lu PT, Wu CR, Lin PC. Chen WC, et al. Among authors: kuo yl. Pediatr Blood Cancer. 2024 Dec;71(12):e31332. doi: 10.1002/pbc.31332. Epub 2024 Sep 17. Pediatr Blood Cancer. 2024. PMID: 39289866

2

Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.

Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY. Kuo YL, et al. Taiwan J Obstet Gynecol. 2014 Jun;53(2):248-51. doi: 10.1016/j.tjog.2014.04.021. Taiwan J Obstet Gynecol. 2014. PMID: 25017279 Free article.

3

Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation.

Chen CP, Lin SP, Chern SR, Kuo YL, Wu PS, Chen YT, Lee MS, Wang W. Chen CP, et al. Among authors: kuo yl. Gene. 2014 Feb 1;535(1):88-92. doi: 10.1016/j.gene.2013.11.026. Epub 2013 Nov 23. Gene. 2014. PMID: 24279999

4

Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature.

Chen CP, Huang MC, Chern SR, Kuo YL, Chen YN, Wu PS, Chen LF, Pan CW, Wang W. Chen CP, et al. Among authors: kuo yl. Taiwan J Obstet Gynecol. 2015 Jun;54(3):297-302. doi: 10.1016/j.tjog.2015.04.001. Taiwan J Obstet Gynecol. 2015. PMID: 26166345 Free article. Review.

5

Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Kuo YL, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. Chen CP, et al. Among authors: kuo yl. Taiwan J Obstet Gynecol. 2020 Mar;59(2):327-330. doi: 10.1016/j.tjog.2020.01.026. Taiwan J Obstet Gynecol. 2020. PMID: 32127159 Free article.

6

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.

Chen CP, Lin CJ, Chern SR, Liu YP, Kuo YL, Chen YN, Wu PS, Town DD, Chen LF, Yang CW, Wang W. Chen CP, et al. Among authors: kuo yl. Taiwan J Obstet Gynecol. 2014 Dec;53(4):583-7. doi: 10.1016/j.tjog.2014.10.002. Taiwan J Obstet Gynecol. 2014. PMID: 25510705 Free article.

7

Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia.

Chen CP, Su YN, Lin MH, Wang TY, Chern SR, Kuo YL, Chen YT, Wang W. Chen CP, et al. Among authors: kuo yl. Taiwan J Obstet Gynecol. 2014 Mar;53(1):68-73. doi: 10.1016/j.tjog.2013.10.036. Taiwan J Obstet Gynecol. 2014. PMID: 24767650 Free article.

8

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.

Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W. Chen CP, et al. Among authors: kuo yl. Taiwan J Obstet Gynecol. 2014 Mar;53(1):90-4. doi: 10.1016/j.tjog.2013.12.003. Taiwan J Obstet Gynecol. 2014. PMID: 24767654 Free article.

9

A Hypoechoic Lesion in the Lung of a Fetus at 22 Weeks of Gestation.

Chang WH, Kuo YL, Chan TF, Li HR, Wu CC, Jaw TS, Ker CR, Hsiao TW. Chang WH, et al. Among authors: kuo yl. J Med Ultrasound. 2017 Jul-Sep;25(3):187. doi: 10.1016/j.jmu.2017.03.007. Epub 2017 Mar 31. J Med Ultrasound. 2017. PMID: 30065488 Free PMC article. No abstract available.

10

A Hypoechoic Lesion in the Lung of a Fetus at 22 Weeks of Gestation.

Chang WH, Kuo YL, Chan TF, Li HR, Wu CC, Jaw TS, Ker CR, Hsiao TW. Chang WH, et al. Among authors: kuo yl. J Med Ultrasound. 2017 Oct-Dec;25(4):251-254. doi: 10.1016/j.jmu.2017.03.008. Epub 2017 Mar 31. J Med Ultrasound. 2017. PMID: 30065503 Free PMC article. No abstract available.

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