Lin YH - Search Results

1

Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chen CP, Kuo YT, Lin SP, Su YN, Chen YJ, Hsueh RY, Lin YH, Wu PC, Lee CC, Chen YT, Wang W. Chen CP, et al. Among authors: lin sp, lin yh. Taiwan J Obstet Gynecol. 2010 Sep;49(3):327-32. doi: 10.1016/S1028-4559(10)60069-1. Taiwan J Obstet Gynecol. 2010. PMID: 21056319 Free article.

2

Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).

Chen CP, Lin YH, Au HK, Su YN, Hsu CY, Liu YP, Wu PC, Chern SR, Chen YT, Chen LF, Hsieh AH, Wang W. Chen CP, et al. Among authors: lin yh. Taiwan J Obstet Gynecol. 2011 Sep;50(3):359-65. doi: 10.1016/j.tjog.2011.07.004. Taiwan J Obstet Gynecol. 2011. PMID: 22030053 Free article.

3

Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.

Chen CP, Lin YH, Chou SY, Su YN, Chern SR, Chen YT, Town DD, Chen WL, Wang W. Chen CP, et al. Among authors: lin yh. Taiwan J Obstet Gynecol. 2012 Mar;51(1):71-6. doi: 10.1016/j.tjog.2012.01.014. Taiwan J Obstet Gynecol. 2012. PMID: 22482972 Free article.

4

Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosomes.

Chen CP, Chen M, Ma GC, Su YN, Ko TM, Lin YH, Wang W. Chen CP, et al. Among authors: lin yh. J Chin Med Assoc. 2013 Jan;76(1):53-6. doi: 10.1016/j.jcma.2011.10.016. Epub 2012 Dec 23. J Chin Med Assoc. 2013. PMID: 23331783 Free article.

5

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.

Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. Chen CP, et al. Among authors: lin sp, lin yh. Taiwan J Obstet Gynecol. 2016 Dec;55(6):852-855. doi: 10.1016/j.tjog.2016.08.002. Taiwan J Obstet Gynecol. 2016. PMID: 28040132 Free article.

6

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality.

Chen CP, Fu CH, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Chen CP, et al. Among authors: lin yh. Taiwan J Obstet Gynecol. 2016 Dec;55(6):871-873. doi: 10.1016/j.tjog.2016.08.004. Taiwan J Obstet Gynecol. 2016. PMID: 28040137 Free article.

7

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis.

Chen CP, Lin YH, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W. Chen CP, et al. Among authors: lin yh. Taiwan J Obstet Gynecol. 2020 Jan;59(1):146-149. doi: 10.1016/j.tjog.2019.11.024. Taiwan J Obstet Gynecol. 2020. PMID: 32039784 Free article.

8

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Lin YH, Wu PS, Chern SR, Chen SW, Wu FT, Lee CC, Pan CW, Chen YY, Wang W. Chen CP, et al. Among authors: lin yh. Taiwan J Obstet Gynecol. 2022 Jan;61(1):138-140. doi: 10.1016/j.tjog.2021.11.023. Taiwan J Obstet Gynecol. 2022. PMID: 35181025 Free article.

9

Prenatal sonographic diagnosis of acrania associated with amniotic bands.

Chen CP, Chang TY, Lin YH, Wang W. Chen CP, et al. Among authors: lin yh. J Clin Ultrasound. 2004 Jun;32(5):256-60. doi: 10.1002/jcu.20021. J Clin Ultrasound. 2004. PMID: 15124194

10

A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.

Chen CP, Chern SR, Tsai FJ, Lin CY, Lin YH, Wang W. Chen CP, et al. Among authors: lin cy, lin yh. Prenat Diagn. 2005 Apr;25(4):327-30. doi: 10.1002/pd.1123. Prenat Diagn. 2005. PMID: 15849793

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