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 *

195 related articles for article (PubMed ID: 33966748)

  • 1. Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature.
    Hu XN; Li LL; Shi QY; Hu ZM; Zhang HG; Jiang YT; Liu RZ
    Taiwan J Obstet Gynecol; 2021 May; 60(3):554-558. PubMed ID: 33966748
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal origin.
    Chen CP; Chen CY; Chern SR; Chen SW; Wu FT; Chen WL; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2021 Jul; 60(4):771-774. PubMed ID: 34247823
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
    Chen CP; Liou JD; Seow KM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucency.
    Sinajon P; Chitayat D; Roifman M; Wasim S; Carmona S; Ryan G; Noor A; Kolomietz E; Chong K
    Ultrasound Obstet Gynecol; 2020 Mar; 55(3):383-390. PubMed ID: 31115076
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
    Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies.
    He JP; Qian Y; Liu WJ; Tang J; Qin MH; Luo SJ; Hou JH; Lv MX
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):318-323. PubMed ID: 33678334
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a case of partial monosomy/monosomy 13 mosaicism: 46,XX,r(13)(p11q33)/45,XX,-13 suspected by nuchal fold translucency increasing.
    Kataoka A; Hirakawa S; Iwamoto M; Sakumura Y; Yoshinaga R; Ohba T
    Kurume Med J; 2011; 58(4):127-30. PubMed ID: 23047142
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Application of chromosomal microarray in fetuses with increased nuchal translucency.
    Zhao XR; Gao L; Wu Y; Wang YL
    J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
    [No Abstract]   [Full Text] [Related]  

  • 14. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
    Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.
    Chen CP; Lo LM; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):331-334. PubMed ID: 33678337
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of copy number variation by CMA in fetus with increased nuchal translucency].
    Du L; Xie HN; Zheng J; He M
    Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):671-676. PubMed ID: 30369122
    [No Abstract]   [Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency.
    Stembalska A; Jagielska G; Laczmanska I; Szmida E; Jarczynska A; Gil J
    Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):255-9. PubMed ID: 25852029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):852-856. PubMed ID: 29241934
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.