196 related articles for article (PubMed ID: 22490612)
1. Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism.
Robberecht C; Voet T; Utine GE; Schinzel A; de Leeuw N; Fryns JP; Vermeesch J
Mol Cytogenet; 2012 Apr; 5():19. PubMed ID: 22490612
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases.
Kato T; Kawai M; Miyai S; Suzuki F; Tsutsumi M; Mizuno S; Ikeda T; Kurahashi H
Cytogenet Genome Res; 2020; 160(3):118-123. PubMed ID: 32248198
[TBL] [Abstract][Full Text] [Related]
3. Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.
Žilina O; Koltšina M; Raid R; Kurg A; Tõnisson N; Salumets A
BMC Genomics; 2015 Sep; 16(1):703. PubMed ID: 26376747
[TBL] [Abstract][Full Text] [Related]
4. Confined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer.
Valind A; Pal N; Asmundsson J; Gisselsson D; Holmquist Mengelbier L
Genes Chromosomes Cancer; 2014 Jul; 53(7):634-8. PubMed ID: 24729308
[TBL] [Abstract][Full Text] [Related]
5. Germ-line transmission of trisomy 21: Data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue.
Kovaleva NV
Mol Cytogenet; 2010 Mar; 3():7. PubMed ID: 20298592
[TBL] [Abstract][Full Text] [Related]
6. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.
Robinson WP; Bernasconi F; Lau A; McFadden DE
Am J Med Genet; 1999 May; 84(1):34-42. PubMed ID: 10213044
[TBL] [Abstract][Full Text] [Related]
7. Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.
Robinson WP; Barrett IJ; Bernard L; Telenius A; Bernasconi F; Wilson RD; Best RG; Howard-Peebles PN; Langlois S; Kalousek DK
Am J Hum Genet; 1997 Apr; 60(4):917-27. PubMed ID: 9106539
[TBL] [Abstract][Full Text] [Related]
8. Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.
Kalousek DK; Langlois S; Robinson WP; Telenius A; Bernard L; Barrett IJ; Howard-Peebles PN; Wilson RD
Am J Med Genet; 1996 Nov; 65(4):348-52. PubMed ID: 8923948
[TBL] [Abstract][Full Text] [Related]
9. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
Conlin LK; Thiel BD; Bonnemann CG; Medne L; Ernst LM; Zackai EH; Deardorff MA; Krantz ID; Hakonarson H; Spinner NB
Hum Mol Genet; 2010 Apr; 19(7):1263-75. PubMed ID: 20053666
[TBL] [Abstract][Full Text] [Related]
10. Mosaic trisomy 13: understanding origin using SNP array.
Jinawath N; Zambrano R; Wohler E; Palmquist MK; Hoover-Fong J; Hamosh A; Batista DA
J Med Genet; 2011 May; 48(5):323-6. PubMed ID: 21097773
[TBL] [Abstract][Full Text] [Related]
11. Origin and mechanisms of non-disjunction in human autosomal trisomies.
Nicolaidis P; Petersen MB
Hum Reprod; 1998 Feb; 13(2):313-9. PubMed ID: 9557829
[TBL] [Abstract][Full Text] [Related]
12. Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.
Minelli A; Morerio C; Maserati E; Olivieri C; Panarello C; Bonvini L; Leszl A; Rosanda C; Lanino E; Danesino C; Pasquali F
Leukemia; 2001 Jun; 15(6):971-5. PubMed ID: 11417485
[TBL] [Abstract][Full Text] [Related]
13. Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
Bruyère H; Rupps R; Kuchinka BD; Friedman JM; Robinson WP
Am J Med Genet; 2000 Sep; 94(1):35-41. PubMed ID: 10982480
[TBL] [Abstract][Full Text] [Related]
14. Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities.
Baidas S; Chen TJ; Kolev V; Wong LJ; Imholte J; Qin N; Meck J
Am J Med Genet A; 2004 Feb; 124A(4):383-7. PubMed ID: 14735586
[TBL] [Abstract][Full Text] [Related]
15. Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
Karadima G; Bugge M; Nicolaidis P; Vassilopoulos D; Avramopoulos D; Grigoriadou M; Albrecht B; Passarge E; Annerén G; Blennow E; Clausen N; Galla-Voumvouraki A; Tsezou A; Kitsiou-Tzeli S; Hahnemann JM; Hertz JM; Houge G; Kuklík M; Macek M; Lacombe D; Miller K; Moncla A; López Pajares I; Patsalis PC; Petersen MB
Eur J Hum Genet; 1998; 6(5):432-8. PubMed ID: 9801867
[TBL] [Abstract][Full Text] [Related]
16. Origin of acrocentric trisomies in spontaneous abortuses.
Niikawa N; Merotto E; Kajii T
Hum Genet; 1977 Dec; 40(1):73-8. PubMed ID: 604246
[TBL] [Abstract][Full Text] [Related]
17. Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.
Ripperger T; Tauscher M; Praulich I; Pabst B; Teigler-Schlegel A; Yeoh A; Göhring G; Schlegelberger B; Flotho C; Niemeyer CM; Steinemann D
Br J Haematol; 2011 Oct; 155(2):209-17. PubMed ID: 21848520
[TBL] [Abstract][Full Text] [Related]
18. Frequencies of chromosome-specific mosaicisms in trophoectoderm biopsies detected by next-generation sequencing.
Nakhuda G; Jing C; Butler R; Guimond C; Hitkari J; Taylor E; Tallon N; Yuzpe A
Fertil Steril; 2018 May; 109(5):857-865. PubMed ID: 29778385
[TBL] [Abstract][Full Text] [Related]
19. Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.
Devriendt K; Matthijs G; Claes S; Legius E; Proesmans W; Cassiman JJ; Fryns JP
J Med Genet; 1997 Apr; 34(4):318-22. PubMed ID: 9138157
[TBL] [Abstract][Full Text] [Related]
20. The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?
Zuffardi O; Fichera M; Bonaglia MC
Eur J Med Genet; 2022 Aug; 65(8):104532. PubMed ID: 35724817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
