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 *

196 related articles for article (PubMed ID: 19565618)

  • 21. [A case of 18-trisomy diagnosed by fluorescence in situ hybridization of amniocyte].
    Maruyama H; Fukushi Y; Tando T; Wada J; Niino T; Sato S; Kagiya A; Sato S; Saito Y
    Nihon Sanka Fujinka Gakkai Zasshi; 1994 Jul; 46(7):611-3. PubMed ID: 8089600
    [No Abstract]   [Full Text] [Related]  

  • 22. Prenatally diagnosed mosaic trisomy 17: a case report with two-year follow-up.
    Abrams DJ; Augustyn AM; Geier MR
    Prenat Diagn; 2005 Oct; 25(10):968-9. PubMed ID: 16193466
    [No Abstract]   [Full Text] [Related]  

  • 23. [A case of trisomy 19 pseudomosaicism--originated an extra fetal organ].
    Yamada N; Hamada H; Sohda S; Kubo T
    Nihon Sanka Fujinka Gakkai Zasshi; 1995 Dec; 47(12):1378-80. PubMed ID: 8568359
    [No Abstract]   [Full Text] [Related]  

  • 24. Prenatal diagnosis of mosaicism for trisomy 16 in a single colony at amniocentesis with a favorable outcome.
    Yan Z; Cui W; Zeng X; Chen X
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):374-375. PubMed ID: 33678348
    [No Abstract]   [Full Text] [Related]  

  • 25. Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis with a favorable outcome.
    Tang W; Zhang Q; Yue Z; Li F; Tang X
    Taiwan J Obstet Gynecol; 2020 Mar; 59(2):344-345. PubMed ID: 32127164
    [No Abstract]   [Full Text] [Related]  

  • 26. Prenatally detected double trisomy: Klinefelter and Down syndrome.
    Sanz-Cortés M; Raga F; Cuesta A; Claramunt R; Bonilla-Musoles F
    Prenat Diagn; 2006 Nov; 26(11):1078-80. PubMed ID: 16958145
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of low-level mosaic trisomy 6 by amniocentesis.
    Chen CP; Chern SR; Lee PY; Town DD; Wang W
    Prenat Diagn; 2006 Nov; 26(11):1093-6. PubMed ID: 17072899
    [No Abstract]   [Full Text] [Related]  

  • 28. Comparison of modes of ascertainment for mosaic vs complete trisomy 21.
    Bornstein E; Lenchner E; Donnenfeld A; Kapp S; Keeler SM; Divon MY
    Am J Obstet Gynecol; 2009 Apr; 200(4):440.e1-5. PubMed ID: 19318154
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A 46,XY/46,XX mosaicism diagnosed at amniocentesis: another case report.
    Liao C; Yang X; Pan M; Li DZ
    Prenat Diagn; 2008 Jan; 28(1):65-6. PubMed ID: 18058977
    [No Abstract]   [Full Text] [Related]  

  • 30. Prenatal diagnosis of 47,XXX.
    Khoury-Collado F; Wehbeh AN; Fisher AJ; Bombard AT; Weiner Z
    Am J Obstet Gynecol; 2005 May; 192(5):1469-71. PubMed ID: 15902140
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Agenesis of the ductus venosus in a fetus with nonmosaic trisomy 22.
    Barseghyan K; Sklansky MS; Paquette LB; Randolph LM; Miller DA
    Prenat Diagn; 2009 Sep; 29(9):901-2. PubMed ID: 19499517
    [No Abstract]   [Full Text] [Related]  

  • 32. Amniotic fluid angiogenin levels are decreased in pregnancies with fetal trisomy 21.
    Demir A; Guclu S; Bige O; Solak A; Demir N
    Prenat Diagn; 2011 Nov; 31(11):1101-3. PubMed ID: 21800332
    [No Abstract]   [Full Text] [Related]  

  • 33. Counseling patients with trisomy 17 mosaicism found at genetic amniocentesis.
    Collado FK; Fisher AJ; Bombard AT
    Prenat Diagn; 2003 Nov; 23(11):948-50. PubMed ID: 14634987
    [No Abstract]   [Full Text] [Related]  

  • 34. Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia.
    Tan D; Lau LC; Teng LM; Sane S; Lim TH; Tien SL
    Cancer Genet Cytogenet; 2008 Jan; 180(1):79-82. PubMed ID: 18068540
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Real-time quantitative PCR for the detection of fetal aneuploidies.
    Zimmermann BG; Dudarewicz L
    Methods Mol Biol; 2008; 444():95-109. PubMed ID: 18425474
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mosaicism for trisomy 21 in a patient with young-onset dementia: a case report and brief literature review.
    Ringman JM; Rao PN; Lu PH; Cederbaum S
    Arch Neurol; 2008 Mar; 65(3):412-5. PubMed ID: 18332257
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Another rare prenatal case of post-zygotic mosaic trisomy 17.
    de Vries FA; Govaerts LC; Knijnenburg J; Knapen MF; Oudesluijs GG; Lont D; Noomen P; de Graaff K; Srebniak MI; Van Opstal D
    Am J Med Genet A; 2013 May; 161A(5):1196-9. PubMed ID: 23512336
    [No Abstract]   [Full Text] [Related]  

  • 38. Parental mosaicism for trisomy 21: problems with its detection and an approach to determining its population rate.
    Kovaleva NV
    Genet Test; 2007; 11(3):341-4. PubMed ID: 17949298
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetic counseling in prenatally diagnosed trisomy 18 and 21: psychosocial aspects.
    Adler B; Kushnick T
    Pediatrics; 1982 Jan; 69(1):94-9. PubMed ID: 6459565
    [No Abstract]   [Full Text] [Related]  

  • 40. A non-mosaic tetraploidy in the long-term culture of chorionic villi with a trisomy 13 in concomitant amniocytes.
    Sikkema-Raddatz B; Bouman K; Drok G; ter Brugge HG; Suijkerbuijk R
    Prenat Diagn; 2009 May; 29(5):541-2. PubMed ID: 19222025
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.