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Journal Abstract Search

724 related items for PubMed ID: 25608988

  • 21. The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities.
    Ye F, Xu X, Wang Y, Chen L, Shan Q, Wang Q, Jin F.
    BMC Pregnancy Childbirth; 2024 Apr 05; 24(1):244. PubMed ID: 38580914
    [Abstract] [Full Text] [Related]

  • 22. Congenital heart defects and copy number variants associated with neurodevelopmental impairment.
    Findley TO, Crain AK, Mahajan S, Deniwar A, Davis J, Solis Zavala AS, Corno AF, Rodriguez-Buritica D.
    Am J Med Genet A; 2022 Jan 05; 188(1):13-23. PubMed ID: 34472185
    [Abstract] [Full Text] [Related]

  • 23. Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
    Sukenik-Halevy R, Sukenik S, Koifman A, Alpert Y, Hershkovitz R, Levi A, Biron-Shental T.
    Prenat Diagn; 2016 Dec 05; 36(13):1185-1191. PubMed ID: 27794172
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  • 24. The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
    Wu Y, Wang Y, Tao J, Han X, Zhao X, Liu C, Gao L, Cheng W.
    Eur J Obstet Gynecol Reprod Biol; 2017 May 05; 212():44-50. PubMed ID: 28340467
    [Abstract] [Full Text] [Related]

  • 25. Chromosomal microarray analysis for the detection of chromosome abnormalities in fetuses with echogenic intracardiac focus in women without high-risk factors.
    He M, Zhang Z, Hu T, Liu S.
    Medicine (Baltimore); 2020 Jan 05; 99(5):e19014. PubMed ID: 32000445
    [Abstract] [Full Text] [Related]

  • 26. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
    Deng Q, Fu F, Li R, Jing X, Lei T, Yang X, Pan M, Zhen L, Han J, Liao C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct 10; 34(5):699-704. PubMed ID: 28981937
    [Abstract] [Full Text] [Related]

  • 27. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
    Fu F, Deng Q, Lei TY, Li R, Jing XY, Yang X, Liao C.
    Arch Gynecol Obstet; 2017 Nov 10; 296(5):929-940. PubMed ID: 28905115
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  • 28. Selection of prenatal screening with nuchal translucency > 95th centile and below 99th centile: a 4-year observational study with real-world data.
    Zhang B, Zhang LX, Yi J, Wang CH, Zhao Y.
    Arch Gynecol Obstet; 2024 Sep 10; 310(3):1779-1785. PubMed ID: 38625542
    [Abstract] [Full Text] [Related]

  • 29. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
    Guo YL, Wang L, Xue SW, Qu SZ, Yang J, Xu H, Bai ZX, Liu N, Kong XD.
    Zhonghua Fu Chan Ke Za Zhi; 2018 Jul 25; 53(7):464-470. PubMed ID: 30078256
    [Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing.
    Xing Y, Zhang Y, Chen J, Wu F, Yuan M, Zou G, Yang Y, Zhou F, Zhou J, Sun L.
    Prenat Diagn; 2022 Jun 25; 42(7):873-880. PubMed ID: 35584285
    [Abstract] [Full Text] [Related]

  • 31. [Clinical value of genome-wide chromosome microarray technique in diagnosis of fetal cerebral ventriculomegaly].
    Peng YX, Qiu YW, Chang QX, Yu YH, Zhong M, Li KR.
    Nan Fang Yi Ke Da Xue Xue Bao; 2018 Mar 20; 38(3):353-357. PubMed ID: 29643044
    [Abstract] [Full Text] [Related]

  • 32. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
    Chang Q, Yang Y, Peng Y, Liu S, Li L, Deng X, Yang M, Lan Y.
    Eur J Paediatr Neurol; 2020 Mar 20; 25():106-112. PubMed ID: 32014392
    [Abstract] [Full Text] [Related]

  • 33. How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?
    Hillman SC, McMullan DJ, Silcock L, Maher ER, Kilby MD.
    J Matern Fetal Neonatal Med; 2014 May 20; 27(7):649-57. PubMed ID: 23869996
    [Abstract] [Full Text] [Related]

  • 34. Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
    Xia Y, Yang Y, Huang S, Wu Y, Li P, Zhuang J.
    Prenat Diagn; 2018 May 20; 38(6):406-413. PubMed ID: 29573438
    [Abstract] [Full Text] [Related]

  • 35. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J, Qin Z, Fu H, Luo J, Huang Y, Huang P, Zhang S, Liu T, Lu W, Li W, Jiang T, Wei S, Yang S, Shen Y.
    Ultrasound Obstet Gynecol; 2022 Feb 20; 59(2):226-233. PubMed ID: 34090309
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  • 36. Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.
    Xie X, Huang B, Su L, Cai M, Chen Y, Wu X, Xu L.
    BMC Med Genomics; 2023 Nov 20; 16(1):298. PubMed ID: 37986075
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  • 37. Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
    Wu X, Li Y, Su L, Xie X, Cai M, Lin N, Huang H, Lin Y, Xu L.
    Mol Diagn Ther; 2020 Oct 20; 24(5):611-619. PubMed ID: 32651932
    [Abstract] [Full Text] [Related]

  • 38. Contribution of chromosomal microarray analysis and next-generation sequencing to genetic diagnosis in fetuses with normal karyotype.
    Akalın M, Demirci O, Dizdaroğulları GE, Çiftçi E, Karaman A.
    J Obstet Gynaecol Res; 2023 Feb 20; 49(2):519-529. PubMed ID: 36316250
    [Abstract] [Full Text] [Related]

  • 39. [Application of whole-genome and high-resolution chromosome microarray analysis for the investigation of fetuses with ultrasound abnormalities].
    Zhang Y, Fu F, Li R, Xie G, Han J, Pan M, Zhen L, Yang X, Li D, Liao C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 20; 32(2):169-74. PubMed ID: 25863078
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  • 40. Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray.
    Zhang Z, Hu T, Wang J, Hu R, Li Q, Xiao L, Liao N, Liu Z, Wang H, Liu S.
    Prenat Diagn; 2022 Jan 20; 42(1):79-86. PubMed ID: 34918366
    [Abstract] [Full Text] [Related]

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