These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

295 related items for PubMed ID: 36907182

  • 1. Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
    Zhou Y, Lu X, Zhang Y, Ge Y, Xu Y, Wu L, Jiang Y.
    Cytogenet Genome Res; 2022; 162(7):354-364. PubMed ID: 36907182
    [Abstract] [Full Text] [Related]

  • 2. Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing.
    Shi X, Tang H, Lu J, Yang X, Ding H, Wu J.
    Ann Med; 2021 Dec; 53(1):1285-1291. PubMed ID: 34374610
    [Abstract] [Full Text] [Related]

  • 3. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J, Chen L, Zhou C, Wang L, Xie H, Xiao Y, Zhu H, Hu T, Zhang Z, Zhu Q, Liu Z, Liu S, Wang H, Xu M, Ren Z, Yu F, Cram DS, Liu H.
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
    Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F.
    Hum Genet; 2022 Jan; 141(1):101-126. PubMed ID: 34853893
    [Abstract] [Full Text] [Related]

  • 9. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality].
    She Q, Zhen L, Fu F, Lei TY, Li LS, Li R, Wang D, Zhang YL, Jing XY, Yi CX, Zhong HZ, Tan WH, Li FG, Liao C.
    Zhonghua Fu Chan Ke Za Zhi; 2022 Sep 25; 57(9):671-677. PubMed ID: 36177578
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result.
    Rodriguez-Revenga L, Madrigal I, Borrell A, Martinez JM, Sabria J, Martin L, Jimenez W, Mira A, Badenas C, Milà M.
    Clin Genet; 2020 Oct 25; 98(4):379-383. PubMed ID: 32632923
    [Abstract] [Full Text] [Related]

  • 13. Prenatal genetic testing in 19 fetuses with corpus callosum abnormality.
    She Q, Tang E, Peng C, Wang L, Wang D, Tan W.
    J Clin Lab Anal; 2021 Nov 25; 35(11):e23971. PubMed ID: 34569664
    [Abstract] [Full Text] [Related]

  • 14. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
    Wu X, Fu F, Li R, Pan M, Han J, Zhen L, Yang X, Zhang Y, Li F, Liao C.
    Zhonghua Fu Chan Ke Za Zhi; 2014 Dec 25; 49(12):893-8. PubMed ID: 25608988
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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 25; 212():44-50. PubMed ID: 28340467
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis.
    Chen X, Jiang Y, Zeng S, Zhuang J, Lin N.
    Birth Defects Res; 2024 May 25; 116(5):e2351. PubMed ID: 38766695
    [Abstract] [Full Text] [Related]

  • 18. 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 25; 59(2):226-233. PubMed ID: 34090309
    [Abstract] [Full Text] [Related]

  • 19. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
    Li L, He Z, Huang X, Lin S, Wu J, Huang L, Wan Y, Fang Q.
    Ultrasound Obstet Gynecol; 2020 Apr 25; 55(4):502-509. PubMed ID: 30977228
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.