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2. 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]
3. [Chromosome 18 partial duplication-deficiency by recombination aneusomia in familial pericentric inversion]. Bajolle F; Rose JP; Leroux B; Teyssier JR; Ferrand J; Fandre M Ann Pediatr (Paris); 1980 Apr; 27(4):241-4. PubMed ID: 7224545 [No Abstract] [Full Text] [Related]
4. Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6. Schroer RJ; Culp DM; Stevenson RE; Potts WE; Taylor HA; Simensen RJ Clin Genet; 1980 Jul; 18(1):83-7. PubMed ID: 7418257 [TBL] [Abstract][Full Text] [Related]
5. A case of chromosome 3 duplication q deletion p syndrome born to the mother with a pericentric inversion, inv(3)(p25q21). Kawashima H; Maruyama S Jinrui Idengaku Zasshi; 1979 Mar; 24(1):9-12. PubMed ID: 459148 [No Abstract] [Full Text] [Related]
6. Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1. Mattei JF; Mattei MG; Ardissone JP; Taramasco H; Giraud F Clin Genet; 1980 Feb; 17(2):129-36. PubMed ID: 6244909 [TBL] [Abstract][Full Text] [Related]
7. Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11). Orye E; Benoit Y; van Mele B J Med Genet; 1983 Oct; 20(5):394-6. PubMed ID: 6644772 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Recombinant chromosome 18 resulting from a maternal pericentric inversion. Ayukawa H; Tsukahara M; Fukuda M; Kondoh O Am J Med Genet; 1994 May; 50(4):323-5. PubMed ID: 8209910 [TBL] [Abstract][Full Text] [Related]
10. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect]. Saura R; Longy M; Sautarael M; Renouil M; Sandler B Ann Genet; 1983; 26(3):180-2. PubMed ID: 6606381 [TBL] [Abstract][Full Text] [Related]
11. 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]
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. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22). Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399 [TBL] [Abstract][Full Text] [Related]
14. A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9. Zabel B; Hansen S; Hilig U; Gröting-Imhof H Hum Genet; 1977 Apr; 36(1):117-22. PubMed ID: 858620 [TBL] [Abstract][Full Text] [Related]
15. Paternal pericentric inversion of chromosome 9 with a 9p+ offspring. Honea KL Ala J Med Sci; 1977 Oct; 14(4):434. PubMed ID: 610466 [No Abstract] [Full Text] [Related]
16. A large kindred with an INV(3)(p25q23): clinical, cytogenetic and genetic marker studies. Sutherland GR; Mulley JC; Goldblatt E Ann Genet; 1981; 24(4):202-5. PubMed ID: 6977298 [TBL] [Abstract][Full Text] [Related]
17. Familial pericentric inversion (10) and its effect on two offspring. Rodriguez MT; Martin MJ; Abrisqueta JA J Med Genet; 1984 Aug; 21(4):317-9. PubMed ID: 6492099 [TBL] [Abstract][Full Text] [Related]
18. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18. Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476 [TBL] [Abstract][Full Text] [Related]
19. Meiotic consequences of pericentric inversions of chromosome 13. Wenger SL; Steele MW Am J Med Genet; 1981; 9(4):275-83. PubMed ID: 7294066 [TBL] [Abstract][Full Text] [Related]
20. 9p deletion and distal 9q duplication due to a paternal pericentric inversion 9(p22q32). Sonoda T; Ohba K; Ohdo S; Sameshima K Jinrui Idengaku Zasshi; 1991 Mar; 36(1):111-6. PubMed ID: 2062007 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]