255 related articles for article (PubMed ID: 12407711)
1. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.
Ramadevi AR; Naik U; Dutta U; Srikanth ; Prabhakara K
Am J Med Genet; 2002 Nov; 113(2):190-2. PubMed ID: 12407711
[TBL] [Abstract][Full Text] [Related]
2. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Mosaic pericentric inversion of chromosome 2.
Fryns JP; Petit P; Heffinck R; van den Berghe H
J Genet Hum; 1983 Jun; 31(2):157-61. PubMed ID: 6631425
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a mentally retarded boy with a piebald trait, due to maternal insertion, ins(8;4).
Fujimoto A; Reddy KS; Spinks R
Am J Med Genet; 1998 Jan; 75(1):78-81. PubMed ID: 9450862
[TBL] [Abstract][Full Text] [Related]
6. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
[TBL] [Abstract][Full Text] [Related]
7. The Wolf-Hirschhorn syndrome in adulthood: evaluation of a 24-year-old man with a rec(4) chromosome.
Ogle R; Sillence DO; Merrick A; Ell J; Lo B; Robson L; Smith A
Am J Med Genet; 1996 Oct; 65(2):124-7. PubMed ID: 8911603
[TBL] [Abstract][Full Text] [Related]
8. Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
Vorsanova SG; Iourov IY; Demidova IA; Kolotii AD; Soloviev IV; Yurov YB
Tsitol Genet; 2006; 40(3):45-8. PubMed ID: 16933852
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization.
Morel F; Laudier B; Guérif F; Couet ML; Royère D; Roux C; Bresson JL; Amice V; De Braekeleer M; Douet-Guilbert N
Hum Reprod; 2007 Jan; 22(1):136-41. PubMed ID: 16917123
[TBL] [Abstract][Full Text] [Related]
12. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees.
Nickerson E; Nelson DL
Genomics; 1998 Jun; 50(3):368-72. PubMed ID: 9676431
[TBL] [Abstract][Full Text] [Related]
13. Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case report.
Malan V; Pipiras E; Sifer C; Kanafani S; Cedrin-Durnerin I; Martin-Pont B; Hugues JN; Wolf JP; Benzacken B
Hum Reprod; 2006 Aug; 21(8):2052-6. PubMed ID: 16585123
[TBL] [Abstract][Full Text] [Related]
14. Incidence of breakpoints in pericentric inversions of chromosome 4.
Verma RS; Kleyman SM
Ann Genet; 1996; 39(4):243-5. PubMed ID: 9037353
[TBL] [Abstract][Full Text] [Related]
15. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F
Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482
[TBL] [Abstract][Full Text] [Related]
16. De novo complex chromosome rearrangement: a study of two patients.
Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
[TBL] [Abstract][Full Text] [Related]
17. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
18. Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
Mohammed FM; Krishna Murthy DS; Farag TI; al-Awadi SA; al-Othman SA; Hammad I
Ann Genet; 1993; 36(3):181-5. PubMed ID: 8117067
[TBL] [Abstract][Full Text] [Related]
19. de novo inversion-duplication of 2q35-2qter without growth retardation.
Dahoun-Hadorn S; Bretton-Chappuis B
Ann Genet; 1992; 35(1):55-7. PubMed ID: 1610122
[TBL] [Abstract][Full Text] [Related]
20. [Pericentric inversion of the human Y chromosome].
Motos Guirao MA
An Esp Pediatr; 1989 Dec; 31(6):583-7. PubMed ID: 2698071
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]