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Journal Abstract Search
179 related items for PubMed ID: 699358
1. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11). Carnevale A, Frías S, del Castillo V. Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358 [Abstract] [Full Text] [Related]
2. Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother. Schinzel A. Hum Genet; 1980 Feb; 53(2):169-72. PubMed ID: 7358383 [Abstract] [Full Text] [Related]
3. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations. Brimblecombe FS, Lewis FJ, Vowles M. J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139 [Abstract] [Full Text] [Related]
4. Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11). Binkert F, Stranzinger J, Schinzel A. Hum Hered; 1990 Aug; 40(2):81-4. PubMed ID: 2335369 [Abstract] [Full Text] [Related]
5. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation. Sekhon GS, Taysi K, Rath R. Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241 [Abstract] [Full Text] [Related]
6. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature. Schrander-Stumpel C, Schrander J, Fryns JP, Hamers G. Clin Genet; 1990 Feb 19; 37(2):148-52. PubMed ID: 2178819 [Abstract] [Full Text] [Related]
7. Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations. Nakai H, Yamamoto Y, Kuroki Y. Hum Genet; 1979 Oct 02; 51(3):349-55. PubMed ID: 511169 [No Abstract] [Full Text] [Related]
8. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3). van de Vooren MJ, Planteydt HT, Hagemeijer A, Peters-Slough MF, Timmerman MJ. Clin Genet; 1984 Jan 02; 25(1):52-8. PubMed ID: 6705241 [Abstract] [Full Text] [Related]
9. Trisomy 17p due to A t(5;17) (p15;p11) pat translocation. Jinno Y, Matsuda I, Kajii T. Ann Genet; 1982 Jan 02; 25(2):123-5. PubMed ID: 6984629 [Abstract] [Full Text] [Related]
13. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter. Voss R, Gross-Kieselstein E, Hurvitz H, Dagan J, Kerem E, Zlotogora J. J Med Genet; 1984 Dec 23; 21(6):454-9. PubMed ID: 6512835 [Abstract] [Full Text] [Related]
14. Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations. Parslow M, Chambers D, Drummond M, Hunter W. Hum Genet; 1979 Apr 05; 47(3):253-60. PubMed ID: 457115 [Abstract] [Full Text] [Related]
16. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11). Fryns JP, Casaer P, Van den Berghe H. Hum Genet; 1979 Jan 25; 46(2):237-41. PubMed ID: 422207 [Abstract] [Full Text] [Related]