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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 33678341)

  • 41. [Prenatal diagnosis of chromosome abnormalities and nine microdeletion syndromes using both traditional karyotyping and BoBs].
    Tang XH; Yang BC; Zhu S; Su J; Zhang JM; Yin YF; Feng Y; Li DM; Zhao QF; Yu R; Zhu BS
    Zhonghua Fu Chan Ke Za Zhi; 2016 May; 51(5):325-30. PubMed ID: 27256438
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular cytogenetic characterization of 2q deletion and Xq duplication associated with nasal bone dysplasia in prenatal diagnosis: A case report and literature review.
    Sun ML; Yue FG; Zhang XY; Jiang YT; Li LL; Zhang HG; Liu RZ
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):163-169. PubMed ID: 35181032
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.
    Libotte F; Bizzoco D; Gabrielli I; Mesoraca A; Cignini P; Vitale SG; Marilli I; Gulino FA; Rapisarda AM; Giorlandino C
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review.
    Sun ML; Zhang HG; Liu XY; Yue FG; Jiang YT; Li SB; Liu RZ
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):963-967. PubMed ID: 33218423
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
    Chen CP; Chern SR; Chen YN; Chen SW; Wu PS; Yang CW; Lee CC; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
    [TBL] [Abstract][Full Text] [Related]  

  • 46. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.
    An Y; Amr SS; Torres A; Weissman L; Raffalli P; Cox G; Sheng X; Lip V; Bi W; Patel A; Stankiewicz P; Wu BL; Shen Y
    Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):832-40. PubMed ID: 24019301
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Prenatal diagnosis by chromosomal microarray analysis.
    Levy B; Wapner R
    Fertil Steril; 2018 Feb; 109(2):201-212. PubMed ID: 29447663
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review.
    Chen CP; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):855-858. PubMed ID: 31759542
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.
    Chen CP; Chang TY; Hung FY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):843-846. PubMed ID: 29241932
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.
    Chen CP; Chern SR; Wang LK; Wu PS; Wu FT; Chen YY; Town DD; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):938-940. PubMed ID: 33218416
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genetic effects of a 13q31.1 microdeletion detected by noninvasive prenatal testing (NIPT).
    Jia Y; Zhao H; Shi D; Peng W; Xie L; Wang W; Jiang F; Zhang H; Wang X
    Int J Clin Exp Pathol; 2014; 7(10):7003-11. PubMed ID: 25400788
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Chen CY; Su JW; Chern SR; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):435-9. PubMed ID: 23040932
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prenatal diagnosis and ultrasonographic findings of partial trisomy of chromosome 6q: A case report and review of the literature.
    Li L; Yu Y; Zhang H; Jiang Y; Liu R; Zhang H
    Medicine (Baltimore); 2021 Jan; 100(2):e24091. PubMed ID: 33466173
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):698-703. PubMed ID: 31542096
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villi.
    Anselem O; Bazin A; Mechler C; Blin G; Garel C; Aboura A; Moutard ML; Mandelbrot L
    Fetal Diagn Ther; 2010; 28(3):180-5. PubMed ID: 20829580
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 17q21.31 microdeletion: brain anomalies leading to prenatal diagnosis.
    Egloff M; Encha-Razavi F; Garel C; Bonnière-Darcy M; Millischer AE; Lapierre JM; Fontaine S; de Blois MC; Vekemans M; Turleau C; Ville Y; Malan V
    Cytogenet Genome Res; 2014; 144(3):178-82. PubMed ID: 25402493
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Cytogenetic analysis in fetuses with late onset abnormal sonographic findings.
    Bardin R; Hadar E; Haizler-Cohen L; Gabbay-Benziv R; Meizner I; Kahana S; Yeshaya J; Yacobson S; Cohen-Vig L; Agmon-Fishman I; Basel-Vanagaite L; Maya I
    J Perinat Med; 2018 Nov; 46(9):975-982. PubMed ID: 28915119
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.