96 related articles for article (PubMed ID: 2610490)
1. An unusually large 5q duplication in an adult female subject: spreading of inactivation and in vitro instability of the derivative Xp/5q chromosome.
Rovescalli A; Ghidoni A
Ann Genet; 1989; 32(4):235-40. PubMed ID: 2610490
[TBL] [Abstract][Full Text] [Related]
2. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
[TBL] [Abstract][Full Text] [Related]
3. Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.
Matsuo M; Muroya K; Kosaki K; Ishii T; Fukushima Y; Anzo M; Ogata T
Am J Med Genet; 1999 Sep; 86(1):44-50. PubMed ID: 10440827
[TBL] [Abstract][Full Text] [Related]
4. [Unbalanced translocation 8/X in a girl].
Ickstadt A; Palitzsch D; Foerster W; Fuhrmann-Rieger A
Monatsschr Kinderheilkd; 1989 Apr; 137(4):239-42. PubMed ID: 2733701
[TBL] [Abstract][Full Text] [Related]
5. Partial Xp duplication due to a translocation t(X;15) in two male and two female patients: a familial case report and review of the literature.
Melaragno MI; Ramos MA; Brunoni D
Ann Genet; 1998; 41(4):189-94. PubMed ID: 9881180
[TBL] [Abstract][Full Text] [Related]
6. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2).
Ishikiriyama S; Iai M; Tanabe Y
Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250
[TBL] [Abstract][Full Text] [Related]
7. Multiple congenital anomalies in a man with (X;6) translocation.
Sivak LE; Esbenshade J; Brothman AR; Issa B; Lemons RS; Carey JC
Am J Med Genet; 1994 May; 51(1):9-12. PubMed ID: 8030680
[TBL] [Abstract][Full Text] [Related]
8. Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion.
Yip MY; Kemp J; Hanson N; Wilson M; Purvis-Smith S; Lam-Po-Tang PR
Am J Med Genet; 1989 Jun; 33(2):220-3. PubMed ID: 2764031
[TBL] [Abstract][Full Text] [Related]
9. [Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].
Reichenbach H; Holland H; Thamm B; Theile T
Kinderarztl Prax; 1993 Oct; 61(7-8):291-5. PubMed ID: 8271681
[TBL] [Abstract][Full Text] [Related]
10. Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
Leppig KA; Disteche CM
Semin Reprod Med; 2001 Jun; 19(2):147-57. PubMed ID: 11480912
[TBL] [Abstract][Full Text] [Related]
11. Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation.
Zuffardi O; Tiepolo L; Scappaticci S; Francesconi D; Bianchi C; di Natale D
Ann Genet; 1977 Sep; 20(3):191-94. PubMed ID: 304704
[TBL] [Abstract][Full Text] [Related]
12. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
[TBL] [Abstract][Full Text] [Related]
13. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.
Clark CE; Cowell HR; Telfer MA; Casey PA
Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910
[TBL] [Abstract][Full Text] [Related]
14. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
Morichon-Delvallez N; Couturier J; Frison B
Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
[TBL] [Abstract][Full Text] [Related]
15. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.
Abuelo DN; Ahsanuddin AN; Mark HF
Am J Med Genet; 2000 Oct; 94(5):392-9. PubMed ID: 11050625
[TBL] [Abstract][Full Text] [Related]
16. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
17. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Chen CP; Lin CC; Li YC; Hsieh LJ; Lee CC; Wang W
Fertil Steril; 2006 Nov; 86(5):1514.e1-2. PubMed ID: 17070202
[TBL] [Abstract][Full Text] [Related]
18. Spreading of inactivation in an (X;14) translocation.
Allderdice PW; Miller OJ; Miller DA; Klinger HP
Am J Med Genet; 1978; 2(3):233-40. PubMed ID: 263441
[TBL] [Abstract][Full Text] [Related]
19. Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23.
Kulharya AS; Roop H; Kukolich MK; Nachtman RG; Belmont JW; Garcia-Heras J
Am J Med Genet; 1995 Mar; 56(1):16-21. PubMed ID: 7747779
[TBL] [Abstract][Full Text] [Related]
20. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]