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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]
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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]