BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 35072240)

  • 41. [Application of chromosomal microarray analysis in prenatal diagnosis of pregnant women with advanced age].
    Yang S; Zhao Y; Tang X; Wang Z; Liu D; Zhang J; Gu Y; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):101-107. PubMed ID: 33565058
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
    Yokoyama E; Villarroel CE; Diaz S; Del Castillo V; Pérez-Vera P; Salas C; Gómez S; Barreda R; Molina B; Frias S
    Mol Cytogenet; 2020; 13():42. PubMed ID: 32939224
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
    Zhu H; Lin S; Huang L; He Z; Huang X; Zhou Y; Fang Q; Luo Y
    Prenat Diagn; 2016 Jul; 36(7):686-92. PubMed ID: 27221052
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Prenatal diagnosis of a fetus with chromosome 18p deletion and duplication].
    Li W; Shao H; Yao J; Shi C; Yang X; Zhang J; Zhang X; Shen G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jun; 38(6):569-572. PubMed ID: 34096028
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report.
    Yang H; Huang J; Zheng H; Zhang Y; Zhang Y; Liu W; Wu J; Chen X; Lin J; Ni Y; Nie X
    BMC Med Genomics; 2023 Nov; 16(1):282. PubMed ID: 37946214
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality.
    Nicoulaz A; Rubi F; Lieder L; Wolf R; Goeggel-Simonetti B; Steinlin M; Wiest R; Bonel HM; Schaller A; Gallati S; Conrad B
    Am J Med Genet A; 2011 Aug; 155A(8):1964-8. PubMed ID: 21739569
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Application analysis of noninvasive prenatal testing for fetal chromosome copy number variations in Chinese laboratories].
    Shi JP; Tan P; Li JM; Zhang R
    Zhonghua Yi Xue Za Zhi; 2021 Apr; 101(15):1088-1092. PubMed ID: 33878837
    [No Abstract]   [Full Text] [Related]  

  • 48. Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects.
    Chen CP; Huang JP; Chen SW; Chern SR; Wu PS; Wu FT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):135-139. PubMed ID: 32039782
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report.
    Fitzgibbon GJ; Clayton-Smith J; Banka S; Hamilton SJ; Needham MM; Dore JK; Miller JT; Pawson GD; Gaunt L
    J Med Case Rep; 2008 Nov; 2():355. PubMed ID: 19019217
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.
    Schindewolf E; Khalek N; Johnson MP; Gebb J; Coleman B; Crowley TB; Zackai EH; McDonald-McGinn DM; Moldenhauer JS
    Am J Med Genet A; 2018 Aug; 176(8):1735-1741. PubMed ID: 30055034
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study.
    Fu F; Li R; Yu QX; Dang X; Yan SJ; Zhou H; Cheng K; Huang RB; Wang Y; Zhang YL; Jing XY; Zhang LN; Li DZ; Liao C
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553632
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.
    Maya I; Salzer Sheelo L; Brabbing-Goldstein D; Matar R; Kahana S; Agmon-Fishman I; Klein C; Gurevitch M; Basel-Salmon L; Sagi-Dain L
    Am J Obstet Gynecol; 2022 Apr; 226(4):562.e1-562.e8. PubMed ID: 34762861
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Prenatal diagnosis of fetal multicystic dysplastic kidney via high-resolution whole-genome array.
    Fu F; Chen F; Li R; Zhang Y; Pan M; Li D; Liao C
    Nephrol Dial Transplant; 2016 Oct; 31(10):1693-8. PubMed ID: 26932690
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
    Kurosawa K; Kawame H; Okamoto N; Ochiai Y; Akatsuka A; Kobayashi M; Shimohira M; Mizuno S; Wada K; Fukushima Y; Kawawaki H; Yamamoto T; Masuno M; Imaizumi K; Kuroki Y
    Brain Dev; 2005 Aug; 27(5):378-82. PubMed ID: 16023556
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Cutis laxa in a patient with 1p36 deletion syndrome.
    Zhang Z; Wang J; Li N; Yao R; Chen J
    J Dermatol; 2018 Jul; 45(7):871-873. PubMed ID: 29611295
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Chromosomal deletions detected at amniocentesis.
    Lin CJ; Chen CP; Chien SC; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Lin KC; Yeh TT
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):62-7. PubMed ID: 24767649
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.
    Saito S; Kawamura R; Kosho T; Shimizu T; Aoyama K; Koike K; Wada T; Matsumoto N; Kato M; Wakui K; Fukushima Y
    Am J Med Genet A; 2008 Nov; 146A(22):2891-7. PubMed ID: 18925681
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature.
    Tidrenczel Z; Tardy EP; Pikó H; Sarkadi E; Böjtös I; Demeter J; Simon J; Kósa JP; Beke A
    Cytogenet Genome Res; 2019; 158(2):63-73. PubMed ID: 31261151
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities.
    Song T; Xu Y; Li Y; Jia L; Zheng J; Dang Y; Wan S; Zheng Y; Zhang J; Yang H
    J Clin Lab Anal; 2020 Oct; 34(10):e23434. PubMed ID: 32677110
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion.
    Wang Y; Zhou H; Fu F; Cheng K; Yu Q; Huang R; Lei T; Yang X; Li D; Liao C
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553582
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.