147 related articles for article (PubMed ID: 2746620)
1. A case of two inversion (10) recombinants in a family.
Roberts P; Williams J; Sills MA
J Med Genet; 1989 Jul; 26(7):461-4. PubMed ID: 2746620
[TBL] [Abstract][Full Text] [Related]
2. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
[TBL] [Abstract][Full Text] [Related]
4. A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).
Delicado A; Escribano E; Lopez Pajares I; Diaz de Bustamante A; Carrasco S
J Med Genet; 1991 Feb; 28(2):126-7. PubMed ID: 2002483
[TBL] [Abstract][Full Text] [Related]
5. Abnormal chromosome complement resulting from a familial inversion of chromosome 2.
Richter S; Lockwood B; Lockwood D; Allanson J
J Med Genet; 1989 Nov; 26(11):725-9. PubMed ID: 2479747
[TBL] [Abstract][Full Text] [Related]
6. Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).
Lansky-Shafer SC; Daniel WL; Ruiz L
J Med Genet; 1981 Feb; 18(1):59-61. PubMed ID: 7253000
[TBL] [Abstract][Full Text] [Related]
7. Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversion.
Kulharya AS; Schneider NR; Wilson GN
Am J Med Genet; 1993 Nov; 47(6):817-9. PubMed ID: 8279477
[TBL] [Abstract][Full Text] [Related]
8. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
Battaglia A; Brothman AR; Carey JC
Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
[TBL] [Abstract][Full Text] [Related]
9. Pericentric inversion (13) with two different recombinants in the same family.
Williamson EM; Miller JF; Seabright M
J Med Genet; 1980 Aug; 17(4):309-12. PubMed ID: 7205907
[TBL] [Abstract][Full Text] [Related]
10. Familial 10p trisomy resulting from a maternal pericentric inversion.
Kozma C; Meck JM
Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
[TBL] [Abstract][Full Text] [Related]
11. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
[TBL] [Abstract][Full Text] [Related]
12. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
[TBL] [Abstract][Full Text] [Related]
13. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.
Winsor EJ; Palmer CG; Ellis PM; Hunter JL; Ferguson-Smith MA
Cytogenet Cell Genet; 1978; 20(1-6):169-84. PubMed ID: 648176
[TBL] [Abstract][Full Text] [Related]
14. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
Hirsch B; Baldinger S
Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
[TBL] [Abstract][Full Text] [Related]
15. High recurrence of recombinants in a family with pericentric inversion of chromosome 18.
Mejía-Baltodano G; Bobadilla L; Gonzalez RM; Barros-Núñez P
Ann Genet; 1997; 40(3):164-8. PubMed ID: 9401106
[TBL] [Abstract][Full Text] [Related]
16. Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?
Moedjono SJ; Sparkes RS
Ann Genet; 1980; 23(4):235-7. PubMed ID: 6971603
[TBL] [Abstract][Full Text] [Related]
17. A fetus with recombinant of chromosome 8 inherited from her carrier father.
Fujimoto A; Towner JW; Turkel SB; Wilson MG
Hum Genet; 1978 Feb; 40(3):241-8. PubMed ID: 631845
[TBL] [Abstract][Full Text] [Related]
18. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).
Bocian E; Suchenek K; Obersztyn E; Nowakowska B; Mazurczak T
J Appl Genet; 2005; 46(1):109-14. PubMed ID: 15741672
[TBL] [Abstract][Full Text] [Related]
19. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 10p syndrome owing to maternal pericentric inversion.
Ohba K; Ohdo S; Sonoda T
J Med Genet; 1990 Apr; 27(4):264-6. PubMed ID: 2182876
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
