BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

53 related articles for article (PubMed ID: 29241933)

  • 1. 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]  

  • 2. Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the
    Bonasoni MP; Comitini G; Pati M; Bizzarri V; Barbieri V; Marinelli M; Caraffi SG; Zuntini R; Pollazzon M; Palicelli A; Garavelli L
    Fetal Pediatr Pathol; 2023 Dec; 42(6):979-989. PubMed ID: 37747279
    [No Abstract]   [Full Text] [Related]  

  • 3. Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.
    Salamon I; Park Y; Miškić T; Kopić J; Matteson P; Page NF; Roque A; McAuliffe GW; Favate J; Garcia-Forn M; Shah P; Judaš M; Millonig JH; Kostović I; De Rubeis S; Hart RP; Krsnik Ž; Rasin MR
    Nat Commun; 2023 Sep; 14(1):6025. PubMed ID: 37758766
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1.
    Zhou Y; Quan Y; Wu Y; Zhang Y
    J Int Med Res; 2022 Sep; 50(9):3000605221121955. PubMed ID: 36113068
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):157-160. PubMed ID: 33494993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):432-436. PubMed ID: 32416893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Ko TM; Chen YY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):836-839. PubMed ID: 29241930
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):821-826. PubMed ID: 29241927
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.
    Chen CP; Hsieh CH; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):847-851. PubMed ID: 29241933
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
    Chen CP; Huang MC; Chern SR; Wu PS; Chen SW; Chuang TY; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):692-697. PubMed ID: 31542095
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
    Chen CP; Chen M; Wu CH; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):554-557. PubMed ID: 28805618
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 3.