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fetal polydactyly相关文献:
Polydactyly of the fetal foot: A case report and review of the literature.
Benjamin I, Johns R, Oseji O, Anderson T, Mercardo F, Arruana V, Yancey J, Bogojevic A, Bainbridge R, Toner L, Gaither K.
J Natl Med Assoc. 2022 Aug;114(4):406-411. doi: 10.1016/j.jnma.2022.03.001. Epub 2022 Apr 11.
PMID:35418316
Polydactyly.
Society for Maternal-Fetal Medicine; Rac MWF, McKinney J, Gandhi M.
Am J Obstet Gynecol. 2019 Dec;221(6):B13-B15. doi: 10.1016/j.ajog.2019.09.023.
PMID:31787158
Prenatal diagnosis.
Chueh J.
Curr Opin Obstet Gynecol. 2017 Apr;29(2):71-72. doi: 10.1097/GCO.0000000000000352.
PMID:28253207
Fetal Cyclopia, Proboscis, Holoprosencephaly, and Polydactyly: A Case Report With Review of Literature.
Kollu R, Kotamraju S, Uligada S, Varunya M.
Cureus. 2023 Feb 2;15(2):e34576. doi: 10.7759/cureus.34576. eCollection 2023 Feb.
PMID:36883090
Fetal hydrometrocolpos with pre-axial mirror polydactyly as a new variant of McKusick-Kaufman syndrome.
Traisrisilp K, Nunthapiwat S, Luewan S, Tongsong T.
J Clin Ultrasound. 2021 Jan;49(1):62-65. doi: 10.1002/jcu.22882. Epub 2020 Jun 14.
PMID:32537787
Fetal micromelia, thoracic dysplasia and polydactyly revisited: A case-based antenatal sonographic approach.
Agarwal A, Agarwal S.
Ultrasound. 2019 Aug;27(3):196-201. doi: 10.1177/1742271X19847223. Epub 2019 May 15.
PMID:32549900
Polydactyly, postaxial, type B.
Holmes LB, Nasri H, Hunt AT, Toufaily MH, Westgate MN.
Birth Defects Res. 2018 Jan;110(2):134-141. doi: 10.1002/bdr2.1184.
PMID:29377639
Fetal polydactyly diagnosis during early pregnancy: clinical applications.
Zimmer EZ, Bronshtein M.
Am J Obstet Gynecol. 2000 Sep;183(3):755-8. doi: 10.1067/mob.2000.106974.
PMID:10992205
Phenotypic and genotypic analysis of 11 fetal cases with Bardet-Biedl syndrome.
Yu QX, Liu N, Zhen L, Lin XM, Wen YJ, Li DZ.
Prenat Diagn. 2024 Aug;44(9):1105-1110. doi: 10.1002/pd.6619. Epub 2024 Jun 5.
PMID:38840299
Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure.
Chen CP, Wang LK, Chern SR, Chen SW, Wu FT, Huang SY, Wang W.
Taiwan J Obstet Gynecol. 2022 Jan;61(1):135-137. doi: 10.1016/j.tjog.2021.11.022.
PMID:35181024
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