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3. Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male. Brothman AR; Rehberg K; Storto PD; Phillips SE; Mosby RT Clin Genet; 1992 Jul; 42(1):47-9. PubMed ID: 1516227 [TBL] [Abstract][Full Text] [Related]
4. Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups. Garson OM; Baikie AG; Ferguson J; Greer CH J Med Genet; 1969 Jun; 6(2):209-15. PubMed ID: 5801469 [No Abstract] [Full Text] [Related]
5. Trisomy 14 mosaicism in a 2 year old girl. Petersen MB; Vejerslev LO; Beck B J Med Genet; 1986 Feb; 23(1):86-8. PubMed ID: 3950941 [TBL] [Abstract][Full Text] [Related]
6. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18? Shashi V; Golden WL; von Kap-Herr C; Wilson WG Am J Med Genet; 1996 Mar; 62(1):38-41. PubMed ID: 8779322 [TBL] [Abstract][Full Text] [Related]
7. Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9. Frydman M; Shabtal F; Halbrecht I; Elian E J Med Genet; 1981 Oct; 18(5):390-2. PubMed ID: 7328619 [TBL] [Abstract][Full Text] [Related]
9. Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism. Engel U; Bohlander SK; Bink K; Hinney B; Laccone F; Bartels I Hum Reprod; 2001 Jan; 16(1):63-66. PubMed ID: 11139538 [TBL] [Abstract][Full Text] [Related]
10. Tissue specific mosaicism of trisomy 9 in a patient with severe torsion scoliosis. Morava E; Czakó M; Aszmann M; Illés T; Kosztolányi GY Genet Couns; 2002; 13(4):455-7. PubMed ID: 12558117 [TBL] [Abstract][Full Text] [Related]
11. Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicism. Spinner NB; Grace KR; Owens NL; Sovinsky L; Pellegrino JE; McDonald-McGinn D; Zackai E Am J Med Genet; 1995 Mar; 56(1):22-4. PubMed ID: 7747780 [TBL] [Abstract][Full Text] [Related]
13. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization. Wolstenholme J Prenat Diagn; 1996 Jun; 16(6):511-24. PubMed ID: 8809892 [TBL] [Abstract][Full Text] [Related]
14. 46,X,i(Xq)/47,XX,+13 mosaicism. Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438 [TBL] [Abstract][Full Text] [Related]
15. A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophils. Dallapiccola B; Ferranti G; Giannotti A; Novelli G; Pasquini L; Porfirio B J Med Genet; 1984 Dec; 21(6):467-70. PubMed ID: 6512839 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of mosaic trisomy 8 with investigations of the extent and origin of trisomic cells. Webb AL; Wolstenholme J; Evans J; Macphail S; Goodship J Prenat Diagn; 1998 Jul; 18(7):737-41. PubMed ID: 9706657 [TBL] [Abstract][Full Text] [Related]
17. Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndrome. Reardon PC; Greenstein RM; Howard RO; Gianacopolos EK; Breg WR Am J Med Genet; 1981; 10(2):113-8. PubMed ID: 7315868 [TBL] [Abstract][Full Text] [Related]
18. Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis. Harrison KJ; Barrett IJ; Lomax BL; Kuchinka BD; Kalousek DK Hum Genet; 1993 Oct; 92(4):353-8. PubMed ID: 8225315 [TBL] [Abstract][Full Text] [Related]
19. Analysis of chromosomal equipment in spermatozoa of a 46,XY/47,XY/+8 male by means of multicolour fluorescent in situ hybridization: confirmation of a mosaicism and evaluation of risk for offspring. Mercier S; Bresson JL Hum Genet; 1997 Jan; 99(1):42-6. PubMed ID: 9003492 [TBL] [Abstract][Full Text] [Related]
20. First case of trisomy 13 plus mosaic trisomy 1q. Liehr T; Schmidt M; Starke H; Ziegler M; Kittner G; Heller A; Rubtsov N; Trifonov V; Claussen U Fetal Diagn Ther; 2002; 17(3):133-6. PubMed ID: 11914563 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]