BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 32917332)

  • 41. Prenatal Detection of Trisomy 2: Considerations for Genetic Counseling and Testing.
    Talantova OE; Koltsova AS; Tikhonov AV; Pendina AA; Malysheva OV; Tarasenko OA; Vashukova ES; Shabanova ES; Golubeva AV; Chiryaeva OG; Glotov AS; Bespalova ON; Efimova OA
    Genes (Basel); 2023 Apr; 14(4):. PubMed ID: 37107671
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22.
    Chen CP; Chen M; Ma GC; Chang SP; Chern SR; Chen SW; Wu FT; Chen WL; Lee MS; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Mar; 61(2):364-367. PubMed ID: 35361403
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prenatal Diagnosis and Fetal Outcome with Mosaic Genome-Wide Uniparental Disomy.
    Jawahir-Schonauer J; Norman A; Mbanugo C; Yu G; Rowsey RA; MacDonald E; Romero VC
    Fetal Diagn Ther; 2022; 49(7-8):301-305. PubMed ID: 35981514
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcome.
    Chen CP; Chern SR; Chen SW; Wu FT; Lee CC; Chen WL; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Sep; 61(5):876-879. PubMed ID: 36088060
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Partial Trisomy 4p Syndrome Diagnosed Prenatally.
    Nasri K; Ben Jamaa N; Ouertani I; Boujelben N
    Fetal Pediatr Pathol; 2024; 43(2):188-195. PubMed ID: 37950513
    [No Abstract]   [Full Text] [Related]  

  • 46. High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues.
    Chen CP; Chern SR; Wu PS; Chen SW; Wu FT; Lee CC; Pan CW; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):695-699. PubMed ID: 35779924
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population.
    Zhuang J; Chen C; Huang R; Luo Q; Jiang Y; Zeng S; Wang Y; Xie Y
    Mol Cytogenet; 2022 Jun; 15(1):22. PubMed ID: 35672790
    [TBL] [Abstract][Full Text] [Related]  

  • 48. High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line.
    Chen CP; Chern SR; Chen SW; Wu FT; Lee CC; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):700-702. PubMed ID: 35779925
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q.
    Zhang S; Cui Q; Yang S; Zhang F; Li C; Wang X; Lei B; Sheng X
    BMC Pediatr; 2023 Nov; 23(1):586. PubMed ID: 37993819
    [TBL] [Abstract][Full Text] [Related]  

  • 50. An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22.
    Le TNU; Nguyen VN; Doan TDA; Doan HNB; Le PTQ; Le TL; Ha TMT
    Nagoya J Med Sci; 2020 Nov; 82(4):783-790. PubMed ID: 33311808
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplication.
    Chen CP; Chen SW; Wu PS; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2022 May; 61(3):532-534. PubMed ID: 35595453
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
    Chen CP; Wu FT; Pan YT; Wu PS; Wang W
    Taiwan J Obstet Gynecol; 2024 Jan; 63(1):77-80. PubMed ID: 38216274
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication].
    Zhao J; Gao J; Zhao X; Li L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):617-621. PubMed ID: 38684312
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcome.
    Chen CP; Wu CY; Chern SR; Chen SW; Wu FT; Lee CC; Chen YY; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2022 May; 61(3):525-527. PubMed ID: 35595451
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome.
    Dowlut-McElroy T; Davis S; Howell S; Gutmark-Little I; Bamba V; Prakash S; Patel S; Fadoju D; Vijayakanthi N; Haag M; Hennerich D; Dugoff L; Shankar RK
    Am J Obstet Gynecol; 2022 Dec; 227(6):862-870. PubMed ID: 35841934
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The genotype and phenotype of chromosome 18p deletion syndrome: Case series.
    Jin Q; Qiang R; Cai B; Wang X; Cai N; Zhen S; Zhai W
    Medicine (Baltimore); 2021 May; 100(18):e25777. PubMed ID: 33950970
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Early Diagnosis of 46,XX Testicular Difference of Sexual Development: Unusual Presentation with Increased Nuchal Translucency.
    Saraiva M; Santos VMF; Ramos L; Ramos F; Serra-Caetano J; Cardoso R; Dinis I; Mirante A
    Fetal Pediatr Pathol; 2024; 43(2):176-181. PubMed ID: 37902221
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genetic counseling of a prenatally detected familial 18.79-kb Xp21.1 microduplication encompassing exon 13 of DMD in a pregnancy with no apparent phenotypic abnormalities in the male carriers in the family.
    Chen CP; Lin SP; Wu FT; Pan YT; Wu PS; Wang W
    Taiwan J Obstet Gynecol; 2023 Sep; 62(5):754-756. PubMed ID: 37679008
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound.
    Chen CP
    Taiwan J Obstet Gynecol; 2024 Mar; 63(2):272-275. PubMed ID: 38485332
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.