"Prenatal Diagnosis"[MeSH] - Search Results

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Year	Number of Results
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2024	488

82,410 results

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Page 1

Health professionals' perspectives on the role of obstetric ultrasonography in maternity care in rural eastern Ethiopia: a qualitative descriptive study.

Tefera M, Mezmur H, Jemal M, Assefa N. Tefera M, et al. BMJ Open. 2024 Apr 23;14(4):e075263. doi: 10.1136/bmjopen-2023-075263. BMJ Open. 2024. PMID: 38658007

A sustained decrease in the systolic/diastolic ratio may be a sign of severe adverse events in the umbilical cord: a report of eight cases.

Zeng YJ, Zhang J, Li YF, Chen YY. Zeng YJ, et al. J Int Med Res. 2024 Apr;52(4):3000605241244763. doi: 10.1177/03000605241244763. J Int Med Res. 2024. PMID: 38656272

[Efficiency of CNV-seq in detecting fetal DMD gene deletion or duplication in prenatal diagnosis].

Qiu X, Guo JJ, Jin CC, He J, Wang L, Yang BC, Zhang YH, Zhu BS, Tang XH. Qiu X, et al. Zhonghua Fu Chan Ke Za Zhi. 2024 Apr 25;59(4):279-287. doi: 10.3760/cma.j.cn112141-20230919-00107. Zhonghua Fu Chan Ke Za Zhi. 2024. PMID: 38644274 Chinese.

Deep learning prediction of renal anomalies for prenatal ultrasound diagnosis.

Miguel OX, Kaczmarek E, Lee I, Ducharme R, Dingwall-Harvey ALJ, Rennicks White R, Bonin B, Aviv RI, Hawken S, Armour CM, Dick K, Walker MC. Miguel OX, et al. Sci Rep. 2024 Apr 19;14(1):9013. doi: 10.1038/s41598-024-59248-4. Sci Rep. 2024. PMID: 38641713 Free PMC article.

Prenatal ultrasound findings and clinical outcomes of uniparental disomy: a retrospective study.

Wu CY, Zhou Y, Yin X, Peng R, Xie HN. Wu CY, et al. BMC Pregnancy Childbirth. 2024 Apr 18;24(1):288. doi: 10.1186/s12884-024-06493-0. BMC Pregnancy Childbirth. 2024. PMID: 38637738 Free PMC article.

Malformations of cortical development: Fetal imaging and genetics.

Wang LL, Pan PS, Ma H, He C, Qin ZL, He W, Huang J, Tan SY, Meng DH, Wei HW, Yin AH. Wang LL, et al. Mol Genet Genomic Med. 2024 Apr;12(4):e2440. doi: 10.1002/mgg3.2440. Mol Genet Genomic Med. 2024. PMID: 38634212 Free PMC article.

Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage.

Liu D, Nong X, Lai F, Nong C, Wang T, Tang Y. Liu D, et al. Hemoglobin. 2024 Mar;48(2):71-78. doi: 10.1080/03630269.2024.2327830. Epub 2024 Apr 18. Hemoglobin. 2024. PMID: 38632980

Post-mortem rapid aneuploidy testing for holoprosencephaly.

Gergely L, Repiská V, Böhmer D, Korbeľ M, Václavová Z, McCullough L, Melišová K, Priščáková P. Gergely L, et al. Birth Defects Res. 2024 Apr;116(4):e2342. doi: 10.1002/bdr2.2342. Birth Defects Res. 2024. PMID: 38632851

Comparing three cardiothoracic ratio measurement techniques and creating multivariable scoring system to predict Bart's hydrops fetalis at 17-22 weeks' gestation.

Anuwutnavin S, Rangseechamrat P, Sompagdee N, Ruangvutilert P, Viboonchard S. Anuwutnavin S, et al. Sci Rep. 2024 Apr 17;14(1):8894. doi: 10.1038/s41598-024-59719-8. Sci Rep. 2024. PMID: 38632453 Free PMC article.

Non-syndromic Hirschsprung's disease as a result of a RET gene variant.

Gietz R, Armando R, Lobos P, Liberto D. Gietz R, et al. Cir Pediatr. 2024 Apr 1;37(2):89-92. doi: 10.54847/cp.2024.02.19. Cir Pediatr. 2024. PMID: 38623803 Free article. English, Spanish.

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