268 related articles for article (PubMed ID: 8368250)
1. 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]
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. X-inactivation pattern in three cases of X/autosome translocation.
Zabel BU; Baumann WA; Pirntke W; Gerhard-Ratschow K
Am J Med Genet; 1978; 1(3):309-17. PubMed ID: 677170
[TBL] [Abstract][Full Text] [Related]
4. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The behavior of sex chromosomes in two human X-autosome translocations: failure of extensive X-inactivation spreading.
Solari AJ; Rahn IM; Ferreyra ME; Carballo MA
Biocell; 2001 Aug; 25(2):155-66. PubMed ID: 11590891
[TBL] [Abstract][Full Text] [Related]
7. 45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.
Grompe M; Rao N; Elder FF; Caskey CT; Greenberg F
Am J Med Genet; 1992 Jan; 42(1):39-43. PubMed ID: 1339199
[TBL] [Abstract][Full Text] [Related]
8. X;14 translocation:an exception to the critical region hypothesis on the human X-chromosome.
Markovic VD; Cox DW; Wilkinson J
Am J Med Genet; 1985 Jan; 20(1):87-96. PubMed ID: 3970075
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
11. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Somatic and intellectual development in a patient with 47,XX,psu dic(X)(p11.2) chromosome constitution.
Ocrant I; Bangs CD; Johnston KM; Wilson DM; Hintz RL; Rosenfeld RG; Donlon TA
Am J Med Genet; 1989 Apr; 32(4):536-9. PubMed ID: 2773999
[TBL] [Abstract][Full Text] [Related]
14. Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
Scheuerle A; Zenger-Hain JL; Van Dyke DL; Ledbetter DH; Greenberg F; Shaffer LG
Am J Med Genet; 1995 May; 56(4):403-8. PubMed ID: 7604850
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterization of tiny ring X chromosomes from females with functional X chromosome disomy and lack of cis X inactivation.
Jani MM; Torchia BS; Pai GS; Migeon BR
Genomics; 1995 May; 27(1):182-8. PubMed ID: 7665167
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Unique unbalanced X;X translocation (Xq22;p11.2) in a woman with primary amenorrhea but without Ullrich-Turner syndrome.
Letterie GS
Am J Med Genet; 1995 Dec; 59(4):414-6. PubMed ID: 8585557
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
