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 *

140 related articles for article (PubMed ID: 14679592)

  • 21. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP; Chern SR; Chen YN; Wu PS; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of trisomy 20 mosaicism by maternal serum screening for Down syndrome.
    Chen JH; Hsu TY; Ou CY; Chang LF; Chang SY; Soong YK
    Eur J Obstet Gynecol Reprod Biol; 1999 Oct; 86(2):175-7. PubMed ID: 10509787
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal detection of trisomy 9 mosaicism.
    Schwartz S; Ashai S; Meijboom EJ; Schwartz MF; Sun CC; Cohen MM
    Prenat Diagn; 1989 Aug; 9(8):549-54. PubMed ID: 2798340
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal detection of monosomy 21 mosaicism.
    Ghidini A; Fallet S; Robinowitz J; Lockwood CJ; Dische R; Willner J
    Prenat Diagn; 1993 Mar; 13(3):163-9. PubMed ID: 8506217
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cardiac and extra-cardiac anomalies as indicators for trisomies 13 and 18: a prenatal ultrasound study.
    Wladimiroff JW; Stewart PA; Reuss A; Sachs ES
    Prenat Diagn; 1989 Jul; 9(7):515-20. PubMed ID: 2671976
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
    Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A; Donnai D
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hands and feet in the Apert syndrome.
    Cohen MM; Kreiborg S
    Am J Med Genet; 1995 May; 57(1):82-96. PubMed ID: 7645606
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling.
    Berghella V; Wapner RJ; Yang-Feng T; Mahoney MJ
    Prenat Diagn; 1998 Apr; 18(4):384-9. PubMed ID: 9602487
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Normal outcome of a pregnancy with mosaicism for double trisomy in amniotic fluid cells.
    Bartels I; Franke U; Braulke I; Rauskolb R; Raab-Vetter M
    Prenat Diagn; 1997 Sep; 17(9):877-8. PubMed ID: 9316135
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.
    Sun S; Zhan F; Jiang J; Zhang X; Yan L; Cai W; Liu H; Cao D
    BMC Med Genomics; 2019 Dec; 12(1):197. PubMed ID: 31864361
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM
    Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature review.
    Hu X; Ayala SS; Dyer L; Guan Q; Pena L
    Am J Med Genet A; 2021 Jun; 185(6):1864-1869. PubMed ID: 33759348
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.
    Petit F; Holder-Espinasse M; Duban-Bedu B; Bouquillon S; Boute-Benejean O; Bazin A; Rouland V; Manouvrier-Hanu S; Delobel B
    Clin Genet; 2012 Mar; 81(3):265-71. PubMed ID: 21204802
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fetal blood chromosome analysis: some new indications for prenatal karyotyping.
    Gosden C; Rodeck CH; Nicolaides KH; Campbell S; Eason P; Sharp JC
    Br J Obstet Gynaecol; 1985 Sep; 92(9):915-20. PubMed ID: 4041397
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
    Wieczorek D; Prott EC; Robinson WP; Passarge E; Gillessen-Kaesbach G
    Prenat Diagn; 2003 Feb; 23(2):128-33. PubMed ID: 12575019
    [TBL] [Abstract][Full Text] [Related]  

  • 37. On the significance of true trisomy 20 mosaicism in amniotic fluid culture.
    Djalali M; Steinbach P; Schwinger E; Schwanitz G; Tettenborn U; Wolf M
    Hum Genet; 1985; 69(4):321-6. PubMed ID: 3988281
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Trisomy 18 with unilateral atypical ectrodactyly.
    Rogers RC
    Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239
    [No Abstract]   [Full Text] [Related]  

  • 39. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.
    Martin RA; Jones MC; Jones KL
    Am J Med Genet; 1993 Apr; 46(2):129-31. PubMed ID: 8387244
    [No Abstract]   [Full Text] [Related]  

  • 40. Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literature.
    Zaslav AL; Fallet S; Brown S; Ebert R; Fleischer A; Valderama E; Fox JE
    Clin Genet; 1998 Apr; 53(4):286-92. PubMed ID: 9650767
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.