Lin MH - Search Results

1

Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II.

Chen CP, Chang TY, Lin MH, Chern SR, Su JW, Wang W. Chen CP, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2013 Sep;52(3):420-5. doi: 10.1016/j.tjog.2013.05.003. Taiwan J Obstet Gynecol. 2013. PMID: 24075385 Free article.

2

Distinction between paternal and maternal contributions to the tripronucleus in human zygotes obtained after in vitro fertilization.

Yu SL, Lee RK, Su JT, Chih YF, Tsai YC, Lin MH, Hwu YM. Yu SL, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2006 Dec;45(4):313-6. doi: 10.1016/S1028-4559(09)60249-7. Taiwan J Obstet Gynecol. 2006. PMID: 17175488 Free article.

3

Uterine position change between mock and real embryo transfers.

Yang WJ, Lee RK, Su JT, Lin MH, Hwu YM. Yang WJ, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2007 Jun;46(2):162-5. doi: 10.1016/S1028-4559(07)60011-4. Taiwan J Obstet Gynecol. 2007. PMID: 17638625 Free article.

4

Outcomes of high initial daily doses of gonadotropin in patients with poor ovarian reserve.

Chou LL, Hwu YM, Lin MH, Lin SY, Lee RK. Chou LL, et al. Among authors: lin sy, lin mh. Taiwan J Obstet Gynecol. 2010 Dec;49(4):442-8. doi: 10.1016/S1028-4559(10)60096-4. Taiwan J Obstet Gynecol. 2010. PMID: 21199746 Free article.

5

Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.

Chen CP, Su YN, Tsai FJ, Lin MH, Wu PC, Chern SR, Lee CC, Pan CW, Wang W. Chen CP, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2011 Jun;50(2):205-11. doi: 10.1016/j.tjog.2010.04.001. Taiwan J Obstet Gynecol. 2011. PMID: 21791309 Free article.

6

Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome.

Chen CP, Lin SP, Su YN, Chern SR, Lin MH, Su JW, Wang W. Chen CP, et al. Among authors: lin sp, lin mh. Taiwan J Obstet Gynecol. 2012 Jun;51(2):271-5. doi: 10.1016/j.tjog.2012.04.019. Taiwan J Obstet Gynecol. 2012. PMID: 22795107 Free article.

7

Treatment of infertile women with unilateral tubal occlusion by intrauterine insemination and ovarian stimulation.

Lin MH, Hwu YM, Lin SY, Lee RK. Lin MH, et al. Among authors: lin sy. Taiwan J Obstet Gynecol. 2013 Sep;52(3):360-4. doi: 10.1016/j.tjog.2012.01.037. Taiwan J Obstet Gynecol. 2013. PMID: 24075374 Free article. Clinical Trial.

8

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: lin mh. 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.

9

Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization.

Chen CP, Lin MH, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. Chen CP, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2014 Mar;53(1):123-5. doi: 10.1016/j.tjog.2013.11.002. Taiwan J Obstet Gynecol. 2014. PMID: 24767665 Free article. No abstract available.

10

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.

Chen CP, Lin MH, Chen YY, Chern SR, Chen YN, Wu PS, Pan CW, Lee MS, Wang W. Chen CP, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2015 Oct;54(5):592-6. doi: 10.1016/j.tjog.2015.08.013. Taiwan J Obstet Gynecol. 2015. PMID: 26522117 Free article.

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