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Novel prenatally diagnosed compound heterozygous POMT2 variants in fetal congenital primary aqueduct stenosis.
Taiwan J Obstet Gynecol. 2022 May;61(3):517-520. doi: 10.1016/j.tjog.2022.03.021.
Taiwan J Obstet Gynecol. 2022.
PMID: 35595449
Free article.
Novel prenatally diagnosed compound heterozygous PXDN variants in fetal congenital primary aphakia and blepharophimosis.
Chou WS, Shiao YM, Chen JS, Tsauer JC, Chang YF, Chiu YH, Hsiao CH.
Chou WS, et al. Among authors: tsauer jc.
Taiwan J Obstet Gynecol. 2022 May;61(3):510-513. doi: 10.1016/j.tjog.2022.03.019.
Taiwan J Obstet Gynecol. 2022.
PMID: 35595447
Free article.
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Prenatally diagnosed microdeletion in the TCOF1 gene in fetal congenital primary Treacher Collins Syndrome.
Chou WS, Chen JS, Shiao YM, Tsauer JC, Chang YF, Hsiao CH.
Chou WS, et al. Among authors: tsauer jc.
Taiwan J Obstet Gynecol. 2022 May;61(3):514-516. doi: 10.1016/j.tjog.2022.03.020.
Taiwan J Obstet Gynecol. 2022.
PMID: 35595448
Free article.
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Retrospective analysis of stillbirth and induced termination of pregnancies: Factors affecting determination.
Hsiao CH, Chen CH, Chang YF, Tsauer JC, Chou WS.
Hsiao CH, et al. Among authors: tsauer jc.
Taiwan J Obstet Gynecol. 2022 Jul;61(4):626-629. doi: 10.1016/j.tjog.2022.05.002.
Taiwan J Obstet Gynecol. 2022.
PMID: 35779911
Free article.
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