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3. Dermatoglyphic characteristics of 21-trisomy mosaicism in relation to the fully developed syndrome and normality. Loesch D J Ment Defic Res; 1974 Sep; 18(3):209-69. PubMed ID: 4282743 [No Abstract] [Full Text] [Related]
4. Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element. Guanti G; Maritato F Hum Genet; 1978 Dec; 45(3):355-62. PubMed ID: 153887 [TBL] [Abstract][Full Text] [Related]
5. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q). Vianna-Morgante AM; Nunesmaia HG J Med Genet; 1978 Aug; 15(4):305-10. PubMed ID: 152355 [TBL] [Abstract][Full Text] [Related]
6. Trisomy 21q: 46,XX,21s+/47,XX,+21q-(q22----qter) mosaicism (de novo) in a Down syndrome child. Krishna Murthy DS; Roy S; Contractor PM; Shah VC Indian J Pediatr; 1984; 51(410):363-6. PubMed ID: 6239826 [No Abstract] [Full Text] [Related]
8. Mosaic tetrasomy 21 in a liveborn male infant. Hunter AG; Clifford B; Speevak M; MacMurray SB Clin Genet; 1982 Apr; 21(4):228-32. PubMed ID: 6213323 [No Abstract] [Full Text] [Related]
9. [Down's syndrome with predominantly normal karyotype in lymphocyte culture but extensive G trisomy in fibroblast culture]. Haberlandt W; Wunderlich C Arztl Forsch; 1972 Sep; 26(9):309-16. PubMed ID: 4262890 [No Abstract] [Full Text] [Related]
10. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes. Chen CP; Wang YL; Chern SR; Wu PS; Chen YN; Chen SW; Chen LF; Lee MS; Yang CW; Wang W Taiwan J Obstet Gynecol; 2016 Apr; 55(2):285-7. PubMed ID: 27125416 [TBL] [Abstract][Full Text] [Related]
11. [Down-Turner syndrome (45,X/47,XY,+21): case report and review]. Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340 [TBL] [Abstract][Full Text] [Related]
12. Investigation of 142 mosaic mongols and mosaic parents of mongols; cytogenetic analysis and maternal age at birth. Richards BW J Ment Defic Res; 1974 Sep; 18(3):199-208. PubMed ID: 4282742 [No Abstract] [Full Text] [Related]
13. Free proximal trisomy 21 in the mother and malformation syndrome in the son. Shabtai FS; Schwartz A; Klar D; Hart J; Dar H; Kessler E; Halbrecht I Am J Med Genet Suppl; 1990; 7():182-5. PubMed ID: 2149942 [TBL] [Abstract][Full Text] [Related]
14. Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement. Tharapel AT; Redheendran R; Mankinen CB; Kukolich MK J Med Genet; 1984 Oct; 21(5):391-5. PubMed ID: 6239037 [TBL] [Abstract][Full Text] [Related]
16. A family with three sibs carrying trisomy 21. Nuzzo F; Stefanini M; Simoni G; Larizza L; Mottura A; Reali E; Franceschini P Ann Genet; 1975 Jun; 18(2):111-6. PubMed ID: 127545 [TBL] [Abstract][Full Text] [Related]
17. Secondary nondisjunction causing regular trisomy 21 in the offspring of a mosaic trisomy 21 mother. Krmpotic E; Hardin MB Am J Obstet Gynecol; 1971 Jun; 110(4):589-90. PubMed ID: 4253289 [No Abstract] [Full Text] [Related]
18. Acute myelogenous leukaemia with t(8;21) translocation of normal cell origin in mosaic Down's syndrome with isochromosome 21q. Sato A; Imaizumi M; Koizumi Y; Obara Y; Nakai H; Noro T; Saito T; Saisho T; Yoshinari M; Cui Y; Suzuki H; Funato T; Iinuma K Br J Haematol; 1997 Mar; 96(3):614-6. PubMed ID: 9054671 [TBL] [Abstract][Full Text] [Related]
19. Parental dermatoglyphics in Down's syndrome. A ten-year study. Priest JH; Verhulst C; Sirkin S J Med Genet; 1973 Dec; 10(4):328-32. PubMed ID: 4272738 [TBL] [Abstract][Full Text] [Related]
20. Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and Italy. Schmid W; Tenconi R; Baccichetti C; Caufin D; Schinzel A Am J Med Genet; 1983 Nov; 16(3):323-9. PubMed ID: 6228144 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]