124 related articles for article (PubMed ID: 20420035)
1. Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).
Prontera P; Buldrini B; Aiello V; Rogaia D; Mencarelli A; Gruppioni R; Bonfatti A; Beltrami N; Donti E; Sensi A
Genet Couns; 2010; 21(1):91-7. PubMed ID: 20420035
[TBL] [Abstract][Full Text] [Related]
2. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
Vermeulen SJ; Speleman F; Vanransbeeck L; Verspeet J; Menten B; Verschraegen-Spae MR; Wilde PD; Messiaen L; Michaelis RC; Leroy JG
Eur J Hum Genet; 2005 Jan; 13(1):52-8. PubMed ID: 15470365
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.
Schluth-Bolard C; Till M; Rafat A; Labalme A; Le Lorc'h M; Banquart E; Angei C; Cordier MP; Romana SP; Edery P; Sanlaville D
Eur J Med Genet; 2008; 51(6):622-30. PubMed ID: 18674648
[TBL] [Abstract][Full Text] [Related]
6. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
Garcia-Heras J; Martin J
Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.
Eussen BH; van de Laar I; Douben H; van Kempen L; Hochstenbach R; De Man SA; Van Opstal D; de Klein A; Poddighe PJ
Eur J Med Genet; 2007; 50(2):112-9. PubMed ID: 17161033
[TBL] [Abstract][Full Text] [Related]
15. Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion.
Zamani AG; Acar A; Durakbasi-Dursun G; Yildirim MS; Ceylaner S; Tuncez E
Am J Med Genet A; 2014 May; 164A(5):1239-44. PubMed ID: 24478222
[TBL] [Abstract][Full Text] [Related]
16. Pure familial 6q21q22.1 duplication in two generations.
Pazooki M; Lebbar A; Roubergues A; Baverel F; Letessier D; Dupont JM
Eur J Med Genet; 2007; 50(1):60-5. PubMed ID: 17071147
[TBL] [Abstract][Full Text] [Related]
17. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
[TBL] [Abstract][Full Text] [Related]
18. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A child with a recombinant of chromosome 8 inherited from her carrier mother.
Barnes IC; Kumar D; Bell RJ
J Med Genet; 1985 Feb; 22(1):67-70. PubMed ID: 3981583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
