190 related articles for article (PubMed ID: 20856023)
1. Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.
Baker PR; Tsai AC; Springer M; Swisshelm K; March J; Brown K; Bellus G
J Craniofac Surg; 2010 Sep; 21(5):1369-75. PubMed ID: 20856023
[TBL] [Abstract][Full Text] [Related]
2. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X).
Manea SR; Gershin IF; Babu A; Willner JP; Desnick RJ; Cotter PD
Clin Genet; 1997 Dec; 52(6):432-5. PubMed ID: 9520254
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Characterization of a supernumerary small marker X chromosome in two females with similar phenotypes.
Tümer Z; Wolff D; Silahtaroglu AN; Orum A; Brøndum-Nielsen K
Am J Med Genet; 1998 Feb; 76(1):45-50. PubMed ID: 9508064
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus.
Le Caignec C; Boceno M; Joubert M; Winer N; Aubron F; Fallet-Bianco C; Rival JM
Prenat Diagn; 2003 Feb; 23(2):143-5. PubMed ID: 12575022
[TBL] [Abstract][Full Text] [Related]
8. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
[TBL] [Abstract][Full Text] [Related]
9. Mosaic supernumerary r(8) syndrome.
Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
[No Abstract] [Full Text] [Related]
10. Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis.
Bouayed Abdelmoula N; Portnoï MF; Amouri A; Arladan A; Chakroun M; Saad A; Hchicha M; Turki H; Rebai T
Ann Genet; 2004; 47(3):305-13. PubMed ID: 15337477
[TBL] [Abstract][Full Text] [Related]
11. De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.
Lo-Castro A; El-Malhany N; Galasso C; Verrotti A; Nardone AM; Postorivo D; Palmieri C; Curatolo P
Eur J Med Genet; 2011; 54(3):329-32. PubMed ID: 21333764
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
13. Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12.
Davidsson J; Collin A; Oreberg M; Gisselsson D
Clin Genet; 2008 Jan; 73(1):44-9. PubMed ID: 18005181
[TBL] [Abstract][Full Text] [Related]
14. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
[TBL] [Abstract][Full Text] [Related]
15. Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.
Duncan AM; Macdonald A; Brown CJ; Wolff D; Willard HF; Sutton B
Am J Med Genet; 1993 Dec; 47(8):1153-6. PubMed ID: 8291547
[TBL] [Abstract][Full Text] [Related]
16. Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Chen CP; Kuo YT; Lin SP; Su YN; Chen YJ; Hsueh RY; Lin YH; Wu PC; Lee CC; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2010 Sep; 49(3):327-32. PubMed ID: 21056319
[TBL] [Abstract][Full Text] [Related]
17. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
D'Amato Sizonenko L; Ng D; Oei P; Winship I
Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
[TBL] [Abstract][Full Text] [Related]
18. An atypical Turner syndrome patient with ring X chromosome mosaicism.
Cantú ES; Jacobs DF; Pai GS
Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature.
Bertini V; Valetto A; Uccelli A; Tarantino E; Simi P
Fertil Steril; 2008 Nov; 90(5):2004.e1-5. PubMed ID: 18371955
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]