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.
3. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families. Prieto F; Badia L; Asensi F; Roques V Hum Genet; 1980; 54(1):7-11. PubMed ID: 7390483 [TBL] [Abstract][Full Text] [Related]
4. Three families with abnormal, inherited chromosomes: 2q+mat, t(Cp+; 13q-)mat and t(3?-;5q+)pat. Neu RL; Gardner LI Ann Genet; 1972 Mar; 15(1):19-23. PubMed ID: 4402505 [No Abstract] [Full Text] [Related]
5. A family with a high risk of segregation for an autosomal unbalanced reciprocal translocation. Nielsen J; Rasmussen K; Lassen LB; Christansen F Hum Genet; 1976 Jun; 32(3):343-8. PubMed ID: 939554 [TBL] [Abstract][Full Text] [Related]
6. Inherited translocations in two families (t(14q+;10q-) and t(13q-;21q+)). Talvik T; Mikelsaar AV; Mikelsaar R; Käosaar M; Tüür S Humangenetik; 1973 Sep; 19(3):215-26. PubMed ID: 4763926 [No Abstract] [Full Text] [Related]
8. Familial t(4;13) with abnormal offspring in three generations. Najafzadeh TM; Littman VA; Dumars KW Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065 [TBL] [Abstract][Full Text] [Related]
9. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome. Kitsiou-Tzeli S; Hallett JJ; Atkins L; Latt SA; Holmes LB Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580 [TBL] [Abstract][Full Text] [Related]
10. Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocation. Bonioli E; Crisalli M; Monteverde R; Vianello MG Am J Dis Child; 1981 Dec; 135(12):1115-7. PubMed ID: 7315808 [TBL] [Abstract][Full Text] [Related]
11. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22). Rivera H; Rivas F; Plascencia L; Cantú JM Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704 [TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13). Coco R; del Rey G J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064 [TBL] [Abstract][Full Text] [Related]
13. Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriers. Young RS; Hansen KL; Khodr GS Clin Genet; 1984 Jun; 25(6):522-7. PubMed ID: 6733948 [TBL] [Abstract][Full Text] [Related]
14. Autosomal reciprocal translocations and 13/14 translocations: a population study. Nielsen J; Rasmussen K Clin Genet; 1976 Sep; 10(3):161-77. PubMed ID: 786515 [TBL] [Abstract][Full Text] [Related]
18. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Cohen MM; Ornoy A; Rosenmann A; Kohn G Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372 [TBL] [Abstract][Full Text] [Related]
19. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q. Verma RS; Dosik H; Wexler IB J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332 [TBL] [Abstract][Full Text] [Related]
20. Origin of a paternal (13q;15q) translocation leading to dup(13q) in two half sibs. De los Cobos LF Am J Med Genet; 1983 Apr; 14(4):617-23. PubMed ID: 6846396 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]