These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
233 related articles for article (PubMed ID: 3943862)
1. The significance of pericentric inversions of chromosome 2. Djalali M; Steinbach P; Bullerdiek J; Holmes-Siedle M; Verschraegen-Spae MR; Smith A Hum Genet; 1986 Jan; 72(1):32-6. PubMed ID: 3943862 [TBL] [Abstract][Full Text] [Related]
2. Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Sismani C; Rapti SM; Iliopoulou P; Spring A; Neroutsou R; Lagou M; Robola M; Tsitsopoulos E; Kousoulidou L; Alexandrou A; Papaevripidou I; Theodosiou A; Syrrou M; Fuchs S; Hempel M; Huhle D; Liehr T; Ziegler M; Duesberg M; Velissariou V J Hum Genet; 2020 Sep; 65(9):783-795. PubMed ID: 32398760 [TBL] [Abstract][Full Text] [Related]
3. Familial pericentric inversion of the Y chromosome. Tóth A; Gaál M; László J Ann Genet; 1984; 27(1):60-1. PubMed ID: 6609677 [TBL] [Abstract][Full Text] [Related]
4. Familial pericentric and paracentric inversions of chromosome 1. Johnson DD; Dobyns WB; Gordon H; Dewald GW Hum Genet; 1988 Aug; 79(4):315-20. PubMed ID: 3410456 [TBL] [Abstract][Full Text] [Related]
5. Pericentric inversion of chromosome 19 in three families. D'Alessandro E; De Matteis Vaccarella C; Lo Re ML; Cappa F; D'Alfonso A; Discepoli S; Della Penna MR; Del Porto G Hum Genet; 1988 Oct; 80(2):203-4. PubMed ID: 3169749 [TBL] [Abstract][Full Text] [Related]
6. Pericentric inversion of chromosome 12; a three family study. Haagerup A; Hertz JM Hum Genet; 1992 May; 89(3):292-4. PubMed ID: 1601419 [TBL] [Abstract][Full Text] [Related]
7. A large pericentric inversion of human chromosome 8. Herva R; de la Chapelle A Am J Hum Genet; 1976 May; 28(3):208-12. PubMed ID: 944528 [TBL] [Abstract][Full Text] [Related]
8. Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband. Martin AO; Simpson JL; Deddish RB; Elias S Am J Perinatol; 1983 Oct; 1(1):81-8. PubMed ID: 6680656 [TBL] [Abstract][Full Text] [Related]
9. Cytogenetic studies in reproductive loss. Schmidt R; Nitowsky HM; Dar H JAMA; 1976 Jul; 236(4):369-73. PubMed ID: 947051 [TBL] [Abstract][Full Text] [Related]
11. Pericentric inversions in man: personal experience and review of the literature. Kleczkowska A; Fryns JP; Van den Berghe H Hum Genet; 1987 Apr; 75(4):333-8. PubMed ID: 3570287 [TBL] [Abstract][Full Text] [Related]
12. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. Daniel A; Hook EB; Wulf G Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783 [TBL] [Abstract][Full Text] [Related]
13. A familial pericentric inversion of chromosome 8 analysed with a high resolution chromosome banding technique. Bui TH; Sichong Z; Castro I Clin Genet; 1982 Apr; 21(4):266-71. PubMed ID: 7105473 [TBL] [Abstract][Full Text] [Related]
14. Case report of rec(7)dup(7q)inv(7)(p22q22) and a review of the recombinants resulting from parental pericentric inversions on any chromosomes. Ishii F; Fujita H; Nagai A; Ogihara T; Kim HS; Okamoto R; Mino M Am J Med Genet; 1997 Dec; 73(3):290-5. PubMed ID: 9415687 [TBL] [Abstract][Full Text] [Related]
15. 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]
17. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2. Baccichetti C; Lenzini E; Peserico A; Tenconi R Clin Genet; 1980 Dec; 18(6):402-7. PubMed ID: 7449177 [TBL] [Abstract][Full Text] [Related]
18. Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français. Ann Genet; 1986; 29(3):129-68. PubMed ID: 3538996 [TBL] [Abstract][Full Text] [Related]
19. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9]. Ayral D; Raudrant D; Charleux JP; Noel B Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632 [TBL] [Abstract][Full Text] [Related]
20. Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion. de Perdigo A; Gabriel-Robez O; Rumpler Y Hum Genet; 1989 Oct; 83(3):274-6. PubMed ID: 2793171 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]