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 *

112 related articles for article (PubMed ID: 6934054)

  • 21. Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture.
    Romain DR; Columbano-Green L; Smythe RH; Dukes PC
    Clin Genet; 1979 Sep; 16(3):183-90. PubMed ID: 90568
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal cytogenetic diagnosis: a mini-review.
    Hsu LY
    Prog Clin Biol Res; 1980; 44():3-25. PubMed ID: 6994123
    [No Abstract]   [Full Text] [Related]  

  • 23. Karyotype of amniotic fluid cells at the AUB-MC results on 2000 cases.
    Zahed L; al-Oreibi G; Darwiche N; el-Khechen S
    J Med Liban; 2000; 48(3):121-6. PubMed ID: 11268563
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance.
    Simpson JL; Martin AO; Verp MS; Elias S; Patel VA
    Am J Obstet Gynecol; 1982 Jun; 143(3):250-8. PubMed ID: 7081343
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Extra microchromosome mosaicism in amniotic cells confirmed in fetal tissues.
    Pescia G; Jotterand-Bellomo M; Flury R
    J Genet Hum; 1981 Feb; 28(5):175-83. PubMed ID: 6944439
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Is the 15-in situ clone protocol necessary to detect amniotic fluid mosaicism?
    Cheng EY; Luthy DA; Dunne DF; Luthardt FW; Disteche CM
    Am J Obstet Gynecol; 1995 Oct; 173(4):1025-30. PubMed ID: 7485288
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic counselling for trisomy 20 mosaicism in amniotic fluid cell cultures.
    Nisani R; Chemke J; Rappaport S; Felsenburg T
    Acta Obstet Gynecol Scand; 1984; 63(3):273-5. PubMed ID: 6730946
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Significance of detection of extra metacentric microchromosome in amniotic cell culture.
    Bernstein R; Hakim C; Hardwick B; Nurse GT
    J Med Genet; 1978 Apr; 15(2):136-42. PubMed ID: 641948
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Results and pitfalls in prenatal cytogenetic diagnosis.
    Hsu LY; Dubin EC; Kerenyi T; Hirschhorn K
    J Med Genet; 1973 Jun; 10(2):112-9. PubMed ID: 4268389
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of a 13p+ karyotype.
    Soudek D
    Hum Genet; 1979 Oct; 51(3):339-41. PubMed ID: 511167
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
    Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
    Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
    Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22).
    Arab S; Chitayat D; Gardner HA; Winsor EJ
    Clin Genet; 1999 Nov; 56(5):362-6. PubMed ID: 10668926
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M; Tozzi C; Pomponi MG; Stagni ML; Della Monica M; Scarano G; Calvieri F; Torrisi L; Neri G
    Eur J Hum Genet; 1999; 7(4):421-6. PubMed ID: 10352932
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.
    Chen CP; Ko TM; Chen YY; Su JW; Wang W
    Gene; 2013 Sep; 527(1):384-8. PubMed ID: 23747353
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Parental mosaic trisomy 21 detected following maternal cell contamination of an amniotic fluid specimen from a normal male pregnancy.
    Street ML; Barber JC; Boyle TA; Ellis KH; Bullman H; Homfray T
    Prenat Diagn; 2007 Sep; 27(9):858-60. PubMed ID: 17554802
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM; Tan YQ; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Analysis of mosaic states in amniotic fluid using the in-situ colony technique.
    Welborn JL; Lewis JP
    Clin Genet; 1990 Jul; 38(1):14-20. PubMed ID: 2201467
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS.
    Bernert J; Bartels I; Gatz G; Hansmann I; Heyat M; Niedmann PD; Rehder H; Waldenmaier C; Zoll B
    Am J Med Genet; 1992 Mar; 42(5):747-50. PubMed ID: 1632452
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Counseling dilemmas in the prenatal diagnosis of 45,XO/46,XX mosaicism.
    Hager J; Cortada X; Miller KL; Tedesco TA
    Birth Defects Orig Artic Ser; 1984; 20(6):197-200. PubMed ID: 6535597
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.