147 related articles for article (PubMed ID: 10460414)
1. Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system.
Higgins AW; Schueler MG; Willard HF
Chromosoma; 1999 Aug; 108(4):256-65. PubMed ID: 10460414
[TBL] [Abstract][Full Text] [Related]
2. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
Wolff DJ; Miller AP; Van Dyke DL; Schwartz S; Willard HF
Am J Hum Genet; 1996 Jan; 58(1):154-60. PubMed ID: 8554051
[TBL] [Abstract][Full Text] [Related]
3. Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres.
Sullivan BA; Schwartz S
Hum Mol Genet; 1995 Dec; 4(12):2189-97. PubMed ID: 8634687
[TBL] [Abstract][Full Text] [Related]
4. Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations.
Page SL; Shaffer LG
Chromosome Res; 1998 Feb; 6(2):115-22. PubMed ID: 9543014
[TBL] [Abstract][Full Text] [Related]
5. Extensive cytogenetic analysis of a stable dicentric isochromosome 21, idic(21), formed by fusion of the terminal long arms.
Wandall A; Andersen C; Østergaard M; Koch J
Cytogenet Genome Res; 2002; 97(3-4):145-8. PubMed ID: 12438703
[TBL] [Abstract][Full Text] [Related]
6. Centromere activity in dicentric small supernumerary marker chromosomes.
Ewers E; Yoda K; Hamid AB; Weise A; Manvelyan M; Liehr T
Chromosome Res; 2010 Jul; 18(5):555-62. PubMed ID: 20568005
[TBL] [Abstract][Full Text] [Related]
7. A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.
Lorda-Sanchez I; Binkert F; Maechler M; Schinzel A
Am J Hum Genet; 1991 Nov; 49(5):1034-40. PubMed ID: 1681727
[TBL] [Abstract][Full Text] [Related]
8. Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter).
Daniel A; Saville T; Southall DB
J Med Genet; 1979 Aug; 16(4):278-84. PubMed ID: 490580
[TBL] [Abstract][Full Text] [Related]
9. Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISH.
Page SL; Earnshaw WC; Choo KH; Shaffer LG
Hum Mol Genet; 1995 Feb; 4(2):289-94. PubMed ID: 7757082
[TBL] [Abstract][Full Text] [Related]
10. Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.
Callen DF; Mulley JC; Baker EG; Sutherland GR
Hum Genet; 1987 Nov; 77(3):236-40. PubMed ID: 3479386
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic (Xq).
Gaál M; László J; Bösze P
Hum Genet; 1981; 58(4):362-5. PubMed ID: 7327558
[TBL] [Abstract][Full Text] [Related]
12. Dicentric X isochromosomes in man.
Howell RT; Roberts SH; Beard RJ
J Med Genet; 1976 Dec; 13(6):496-500. PubMed ID: 1018308
[TBL] [Abstract][Full Text] [Related]
13. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
Marozzi A; Manfredini E; Tibiletti MG; Furlan D; Villa N; Vegetti W; Crosignani PG; Ginelli E; Meneveri R; Dalprà L
Hum Genet; 2000 Oct; 107(4):304-11. PubMed ID: 11129329
[TBL] [Abstract][Full Text] [Related]
14. Engineered human dicentric chromosomes show centromere plasticity.
Higgins AW; Gustashaw KM; Willard HF
Chromosome Res; 2005; 13(8):745-62. PubMed ID: 16331407
[TBL] [Abstract][Full Text] [Related]
15. The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.
Therman E; Susman B
Hum Genet; 1990 Jul; 85(2):175-83. PubMed ID: 2370045
[TBL] [Abstract][Full Text] [Related]
16. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.
Daniel A; Lyons N; Casey JH; Gras L
Hum Genet; 1980; 54(1):31-9. PubMed ID: 7190126
[TBL] [Abstract][Full Text] [Related]
17. FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.
Koumbaris G; Hatzisevastou-Loukidou H; Alexandrou A; Ioannides M; Christodoulou C; Fitzgerald T; Rajan D; Clayton S; Kitsiou-Tzeli S; Vermeesch JR; Skordis N; Antoniou P; Kurg A; Georgiou I; Carter NP; Patsalis PC
Hum Mol Genet; 2011 May; 20(10):1925-36. PubMed ID: 21349920
[TBL] [Abstract][Full Text] [Related]
18. Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.
Chadwick BP
Chromosome Res; 2020 Jun; 28(2):155-169. PubMed ID: 31776830
[TBL] [Abstract][Full Text] [Related]
19. Three patients with a 45,X/46,X,psu dic(Xp) karyotype.
Dalton P; Coppin B; James R; Skuse D; Jacobs P
J Med Genet; 1998 Jun; 35(6):519-24. PubMed ID: 9643298
[TBL] [Abstract][Full Text] [Related]
20. FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.
Ogata T; Matsuo N; Fukushima Y; Saito M; Nose O; Miharu N; Uehara S; Ishizuka B
Am J Med Genet; 2001 Dec; 104(4):307-11. PubMed ID: 11754066
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
