177 related articles for article (PubMed ID: 610424)
1. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.
Taylor KM; Francke U; Brown MG; George DL; Kaufhold M
Am J Med Genet; 1977; 1(1):3-19. PubMed ID: 610424
[TBL] [Abstract][Full Text] [Related]
2. Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1.
Jensen PK; Junien C; Despoisse S; Bernsen A; Thelle T; Friedrich U; de la Chapelle A
Ann Genet; 1982; 25(4):207-11. PubMed ID: 6985008
[TBL] [Abstract][Full Text] [Related]
3. U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8.
Mitchell JJ; Vekemans M; Luscombe S; Hayden M; Weber B; Richter A; Sparkes R; Kojis T; Watters G; Der Kaloustian VM
Am J Med Genet; 1994 Feb; 49(4):384-7. PubMed ID: 8160729
[TBL] [Abstract][Full Text] [Related]
4. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
Dierlamm J; Wlodarska I; Michaux L; Vermeesch JR; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman JJ; Mecucci C; Hagemeijer A; Van den Berghe H
Genes Chromosomes Cancer; 1997 Oct; 20(2):155-66. PubMed ID: 9331566
[TBL] [Abstract][Full Text] [Related]
5. [Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band].
Sinet PM; Bresson JL; Couturier J; Laurent C; Prieur M; Rethoré MO; Taillemite JL; Toudic D; Jérome H; Lejeune J
Ann Genet; 1977 Mar; 20(1):13-7. PubMed ID: 302667
[TBL] [Abstract][Full Text] [Related]
6. Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.
Nevin NC; Morrison PJ; Jones J; Reid MM
J Med Genet; 1990 Feb; 27(2):135-6. PubMed ID: 2319583
[TBL] [Abstract][Full Text] [Related]
7. Inverted duplication of 8p: ten new patients and review of the literature.
Feldman GL; Weiss L; Phelan MC; Schroer RJ; Van Dyke DL
Am J Med Genet; 1993 Sep; 47(4):482-6. PubMed ID: 8256810
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Trisomy 20p resulting from inverted duplication and neocentromere formation.
Voullaire L; Saffery R; Davies J; Earle E; Kalitsis P; Slater H; Irvine DV; Choo KH
Am J Med Genet; 1999 Aug; 85(4):403-8. PubMed ID: 10398268
[TBL] [Abstract][Full Text] [Related]
10. Unusual 8p inverted duplication deletion with telomere capture from 8q.
Buysse K; Antonacci F; Callewaert B; Loeys B; Fränkel U; Siu V; Mortier G; Speleman F; Menten B
Eur J Med Genet; 2009; 52(1):31-6. PubMed ID: 19041960
[TBL] [Abstract][Full Text] [Related]
11. Unusual chromosome aberrations in 3 children with Down syndrome.
Osztovics M; Tóth S; Wilhelm O
Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
[TBL] [Abstract][Full Text] [Related]
12. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
13. Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12.
Moreno Fuenmayor HM; Meilinger KL; Rucknagel DL; Mohrenweiser HL; Chu EH
Am J Med Genet; 1980; 7(3):361-8. PubMed ID: 7468661
[TBL] [Abstract][Full Text] [Related]
14. Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.
Kleczkowska A; Fryns JP; D'Hondt F; Jaeken J; Van den Berghe H
Ann Genet; 1987; 30(1):47-51. PubMed ID: 3498429
[TBL] [Abstract][Full Text] [Related]
15. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
Back E; Stier R; Böhm N; Adlung A; Hameister H
Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606
[TBL] [Abstract][Full Text] [Related]
16. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
Barber JC; James RS; Patch C; Temple IK
Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
[TBL] [Abstract][Full Text] [Related]
17. The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm.
Van Dyke DL; Miller MJ; Weiss L
Am J Med Genet; 1983 Jul; 15(3):441-50. PubMed ID: 6881211
[TBL] [Abstract][Full Text] [Related]
18. Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
Antonini S; Kim CA; Sugayama SM; Vianna-Morgante AM
Am J Med Genet; 2002 Nov; 113(2):144-50. PubMed ID: 12407704
[TBL] [Abstract][Full Text] [Related]
19. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA
Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911
[TBL] [Abstract][Full Text] [Related]
20. A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.
Stetten G; Charity LL; Kasch LM; Scott AF; Berman CL; Pressman E; Blakemore KJ
Am J Med Genet; 1997 Jan; 68(1):76-81. PubMed ID: 8986281
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]