152 related articles for article (PubMed ID: 37323193)
1. Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH.
Anlaş Ö; Ölmez A; Karaman B; Düzcan F; Yüksel S; Tümkaya F; Bağcı G; Semerci Gündüz CN
Mol Syndromol; 2023 Jun; 14(3):246-253. PubMed ID: 37323193
[TBL] [Abstract][Full Text] [Related]
2. Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review.
Mules EH; Stamberg J
Hum Genet; 1984; 67(2):126-31. PubMed ID: 6745933
[TBL] [Abstract][Full Text] [Related]
3. A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies.
Kline AD; Griffin CA; Haddadin MH; Chudoba I; Morsberger LA; Hawkins AL; Amato RS; Munshi G; Cohen MM
Am J Med Genet A; 2004 Aug; 129A(2):124-9. PubMed ID: 15316975
[TBL] [Abstract][Full Text] [Related]
4. A new genomic mechanism leading to cri-du-chat syndrome.
South ST; Swensen JJ; Maxwell T; Rope A; Brothman AR; Chen Z
Am J Med Genet A; 2006 Dec; 140(24):2714-20. PubMed ID: 17103439
[TBL] [Abstract][Full Text] [Related]
5. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
Am J Med Genet A; 2003 Apr; 118A(2):333-8. PubMed ID: 12698965
[TBL] [Abstract][Full Text] [Related]
6. Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature.
Douglas C; Smith SA; Rohena L
Am J Med Genet A; 2017 Jun; 173(6):1673-1680. PubMed ID: 28394407
[TBL] [Abstract][Full Text] [Related]
7. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
Phelan MC; Stevenson RE; Anderson EV
Am J Med Genet; 1993 May; 46(3):304-8. PubMed ID: 8488876
[TBL] [Abstract][Full Text] [Related]
8. Paracentric inversions in man.
Fryns JP; Kleczkowska A; Van den Berghe H
Hum Genet; 1986 Jul; 73(3):205-13. PubMed ID: 3733076
[TBL] [Abstract][Full Text] [Related]
9. Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature.
Habhab W; Mau-Holzmann U; Singer S; Rieß A; Kagan KO; Gerbig I; Schäferhoff K; Dufke A; Kehrer M
Am J Med Genet A; 2020 Nov; 182(11):2680-2684. PubMed ID: 32803851
[TBL] [Abstract][Full Text] [Related]
10. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
Bonaglia MC; Fichera M; Marelli S; Romaniello R; Zuffardi O
Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
[TBL] [Abstract][Full Text] [Related]
11. Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl gene.
Kleyman SM; Parekh AJ; Rodriguez AR; Conte RA; Verma RS
Am J Med Genet; 1997 Feb; 68(4):409-11. PubMed ID: 9021012
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects.
Shim SH; Wyandt HE; McDonald-McGinn DM; Zackai EZ; Milunsky A
Clin Genet; 2004 Jul; 66(1):46-52. PubMed ID: 15200507
[TBL] [Abstract][Full Text] [Related]
13. [Paracentric inversions of human chromosomes and their risks].
Balícek P
Cas Lek Cesk; 2004; 143(1):35-8. PubMed ID: 15061117
[TBL] [Abstract][Full Text] [Related]
14. Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.
Devillard F; Guinchat V; Moreno-De-Luca D; Tabet AC; Gruchy N; Guillem P; Nguyen Morel MA; Leporrier N; Leboyer M; Jouk PS; Lespinasse J; Betancur C
Am J Med Genet A; 2010 Sep; 152A(9):2346-54. PubMed ID: 20684015
[TBL] [Abstract][Full Text] [Related]
15. A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.
Worsham MJ; Miller DA; Devries JM; Mitchell AR; Babu VR; Surli V; Weiss L; Van Dyke DL
Am J Hum Genet; 1989 Jan; 44(1):115-23. PubMed ID: 2909165
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. "Cri-du-chat" syndrome in a patient born to a mother with a paracentric inversion of chromosome 5q.
Bourthoumieu S; Esclaire F; Terro F; Baclet MC; Bedu A; Dufetelle B; Gilbert B; Barthe D; Yardin C
Ann Genet; 2003; 46(4):483-6. PubMed ID: 14659787
[TBL] [Abstract][Full Text] [Related]
18. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
Am J Med Genet; 2002 Dec; 113(4):333-8. PubMed ID: 12457404
[TBL] [Abstract][Full Text] [Related]
19. De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently "balanced" paracentric inversion of 14(q21q23).
Jiang YH; Martinez JE; Ou Z; Cooper ML; Kang SH; Pursley A; Cheung SW
Am J Med Genet A; 2008 Aug; 146A(15):1986-93. PubMed ID: 18627051
[TBL] [Abstract][Full Text] [Related]
20. Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss.
Keppler-Noreuil KM; Carroll AJ; Finley SC; Descartes M; Cody JD; DuPont BR; Gay CT; Leach RJ
Am J Med Genet; 1998 Apr; 76(5):372-8. PubMed ID: 9556294
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]