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fetal talipes equinovarus相关文献:
Fetal congenital talipes equinovarus: genomic abnormalities and obstetric follow-up results.
Cai M, Lin J, Que Y, Xu L, Lin N, Huang H.
J Matern Fetal Neonatal Med. 2024 Dec;37(1):2299113. doi: 10.1080/14767058.2023.2299113. Epub 2023 Dec 27.
PMID:38151241
Congenital talipes equinovarus (clubfoot).
Society for Maternal-Fetal Medicine; McKinney J, Rac MWF, Gandhi M.
Am J Obstet Gynecol. 2019 Dec;221(6):B10-B12. doi: 10.1016/j.ajog.2019.09.022.
PMID:31787157
Barth Syndrome.
Ferreira C, Pierre G, Thompson R, Vernon H.
2014 Oct 9 [updated 2020 Jul 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:25299040
Value of the fetal plantar shape in prenatal diagnosis of talipes equinovarus.
Liao H, Cai A, Wang B, Wang X, Yan Z, Li J.
J Ultrasound Med. 2012 Jul;31(7):997-1002. doi: 10.7863/jum.2012.31.7.997.
PMID:22733848
Amniocentesis.
Jindal A, Sharma M, Karena ZV, Chaudhary C.
2023 Aug 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:32644673
Neu Laxova syndrome.
Dwivedi T, Gosavi M.
Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):149-152. doi: 10.4103/IJPM.IJPM_351_17.
PMID:30706883
Outcome of isolated fetal talipes: A systematic review and meta-analysis.
Di Mascio D, Buca D, Khalil A, Rizzo G, Makatsariya A, Sileo F, Liberati M, Benedetti Panici P, Acharya G, D'Antonio F.
Acta Obstet Gynecol Scand. 2019 Nov;98(11):1367-1377. doi: 10.1111/aogs.13637. Epub 2019 Jun 6.
PMID:31034582
SYNE1 Deficiency.
Beaudin M, Gamache PL, Gros-Louis F, Dupré N.
2007 Feb 23 [updated 2018 Dec 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301553
Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study.
Huang R, Yang X, Zhou H, Fu F, Cheng K, Wang Y, Ma C, Li R, Jing X, Han J, Zhen L, Pan M, Li D, Liao C.
Genes (Basel). 2022 Sep 1;13(9):1573. doi: 10.3390/genes13091573.
PMID:36140741
Phenotype of COL3A1/COL5A2 deletion patients.
Kempers MJ, Wessels M, Van Berendoncks A, van de Laar IM, de Leeuw N, Loeys B.
Eur J Med Genet. 2022 Oct;65(10):104593. doi: 10.1016/j.ejmg.2022.104593. Epub 2022 Aug 11.
PMID:35964930
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