123 related articles for article (PubMed ID: 10422813)
1. Ebstein's anomaly associated with trisomy 9p.
Nakagawa M; Kato H; Aotani H; Kondo M
Clin Genet; 1999 May; 55(5):383-5. PubMed ID: 10422813
[No Abstract] [Full Text] [Related]
2. Ebstein's anomaly in an infant with D-1 trisomy syndrome.
Murphy JW; Singh S; Reisman LE
J Ky Med Assoc; 1967 Jun; 65(6):585-6 passim. PubMed ID: 6043882
[No Abstract] [Full Text] [Related]
3. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
4. [Trisomy 22. A new case].
Berger R; Lejeune C; de Paillerets F
Ann Pediatr (Paris); 1976 Nov; 23(11):705-11. PubMed ID: 16106879
[No Abstract] [Full Text] [Related]
5. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
Komatsu H; Kihara A; Komura E; Mitsufuji N; Tsujii H; Kakita S; Ikuta H
Genet Couns; 2001; 12(2):137-43. PubMed ID: 11491308
[TBL] [Abstract][Full Text] [Related]
6. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
[No Abstract] [Full Text] [Related]
7. Down syndrome with tandem 21;21 rearrangement and Ebstein's anomaly--a case report.
Cyrus C; Cyril E; Cherian KM; Kulkarni S; Nallathambi C
Int J Cardiol; 2007 Jan; 115(1):e58-60. PubMed ID: 17098303
[TBL] [Abstract][Full Text] [Related]
8. Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
Tihy F; Lemyre E; Dallaire L; Lemieux N
Am J Med Genet; 2000 Apr; 91(5):383-6. PubMed ID: 10767003
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 22: report of a patient diagnosed as a neonate.
Vohra K; Verma RS; Concepcion L
Dis Markers; 1987 Mar; 5(1):13-8. PubMed ID: 3332254
[TBL] [Abstract][Full Text] [Related]
10. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
Hacihanefioğlu S; Güven GS; Deviren A; Silahtaroğlu AN; Yosunvkaya Fenerci E; Ozkiliç A; Yüksel A
Genet Couns; 2002; 13(1):41-8. PubMed ID: 12017237
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic and molecular analysis of trisomy 9. Case report and review.
Zelante L; Notarangelo A; Croce AI; Piemontese MR; Gasparini P
Ann Genet; 1994; 37(1):21-5. PubMed ID: 8010708
[TBL] [Abstract][Full Text] [Related]
12. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
[TBL] [Abstract][Full Text] [Related]
13. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY.
Scrideli CA; Baruffi MR; Squire JA; Ramos ES; Karaskova J; Heck B; Tone LG
Leuk Res; 2005 Dec; 29(12):1465-7. PubMed ID: 15964069
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
Fryns JP
Genet Couns; 1998; 9(3):229-30. PubMed ID: 9777347
[No Abstract] [Full Text] [Related]
15. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
16. Association of partial trisomy 9 (9pter-->q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly.
Chen CP; Hsu CH; Lin SP; Ho CS; Lee CC; Wang W
Prenat Diagn; 2003 Jun; 23(6):519-20. PubMed ID: 12813773
[No Abstract] [Full Text] [Related]
17. [Trisomy 9p. Report of two new cases].
San Román Muñoz M; Herranz Fernández JL; Tejerina Puente A; Arteaga Manjón-Cabeza R; López Grondona F
An Pediatr (Barc); 2004 Oct; 61(4):336-9. PubMed ID: 15456590
[TBL] [Abstract][Full Text] [Related]
18. Four cases of trisomy 9p syndrome with particular chromosome rearrangements.
Bussani Mastellone C; Giovannucci Uzielli ML; Guarducci S; Nathan G
Ann Genet; 1991; 34(2):115-9. PubMed ID: 1746881
[TBL] [Abstract][Full Text] [Related]
19. Biventricular repair of Ebstein's anomaly with pulmonary atresia in a low birth weight neonate.
Hiramatsu Y; Noma M; Horigome H; Takahashi-Igari M; Sakakibara Y
J Card Surg; 2006; 21(4):421-2. PubMed ID: 16846428
[TBL] [Abstract][Full Text] [Related]
20. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
