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.
145 related articles for article (PubMed ID: 6146563)
21. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. Lee JH; Cho HS; Lee ES; Jung BC Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594 [TBL] [Abstract][Full Text] [Related]
22. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis. Stone D; Ning Y; Guan XY; Kaiser-Kupfer M; Wynshaw-Boris A; Biesecker L Hum Genet; 1996 Oct; 98(4):396-402. PubMed ID: 8792811 [TBL] [Abstract][Full Text] [Related]
23. Trisomy for the short arm of chromosome No. 10. Penchaszadeh VB; Coco R J Genet Hum; 1977 Oct; 25(3):221-7. PubMed ID: 591928 [TBL] [Abstract][Full Text] [Related]
24. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis. Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588 [TBL] [Abstract][Full Text] [Related]
25. Complete trisomy 10p resulting from an extra stable telocentric chromosome. Lozić B; Culić V; Lasan R; Tomasović M; Samija RK; Zemunik T Am J Med Genet A; 2012 Jul; 158A(7):1778-81. PubMed ID: 22628287 [No Abstract] [Full Text] [Related]
26. De novo trisomy 4pter leads to q21. Herva R; von Wendt L Hum Genet; 1978 Mar; 41(2):225-30. PubMed ID: 640656 [TBL] [Abstract][Full Text] [Related]
27. [Trisomy 10 p. A previously reported case explained by binding]. Turleau C; Doussau de Bazignan M; Roubin M; de Grouchy J Ann Genet; 1976 Mar; 19(1):61-4. PubMed ID: 1084125 [TBL] [Abstract][Full Text] [Related]
28. Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p. Mattei JF; Mattei MG; Ardissone JP; Coignet J; Giraud F Hum Genet; 1980; 53(3):315-21. PubMed ID: 7372335 [TBL] [Abstract][Full Text] [Related]
29. Partial trisomy 10p and familial translocation t(7;10)(p22;p12). Johnson G; Bachman R; Roed T; Riddervold P Hum Genet; 1977 Mar; 35(3):353-6. PubMed ID: 844878 [TBL] [Abstract][Full Text] [Related]
30. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment. García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157 [TBL] [Abstract][Full Text] [Related]
31. Phenotypic and cytogenetic spectrum of 9p trisomy. Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299 [TBL] [Abstract][Full Text] [Related]
32. Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat. de Chieri P; Spatuzza E; Bonich JM Hum Genet; 1978 Nov; 45(1):71-5. PubMed ID: 730183 [TBL] [Abstract][Full Text] [Related]
33. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication. Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659 [TBL] [Abstract][Full Text] [Related]
34. Partial trisomy 12q associated with a familial translocation. Hemming L; Brown R Clin Genet; 1979 Jul; 16(1):25-8. PubMed ID: 477011 [TBL] [Abstract][Full Text] [Related]
35. [The gene-dose effect for peptidase A on the erythrocytes of a patient with Edwards' syndrome]. Spano B; Balata A; Sanna MG; Fogu G; Angius AG; Sanna R; Congiu AM Pediatr Med Chir; 1990; 12(4):393-4. PubMed ID: 2075105 [TBL] [Abstract][Full Text] [Related]
36. Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomy. Steinbach P; Benz R Hum Genet; 1983; 63(3):290-1. PubMed ID: 6303943 [TBL] [Abstract][Full Text] [Related]
38. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review. Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200 [TBL] [Abstract][Full Text] [Related]
39. Evidence for the assignment of GUK 1 gene locus to 1q32 leads to q43 segment from gene dosage effect. Dallapiccola B; Lungarotti MS; Falorni A; Magnani M; Dacha M Ann Genet; 1980; 23(2):83-5. PubMed ID: 6249178 [TBL] [Abstract][Full Text] [Related]
40. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13). Cetin Z; Mihci E; Keser I; Luleci G Genet Couns; 2012; 23(2):207-14. PubMed ID: 22876579 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]