348 related articles for article (PubMed ID: 15715166)
1. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Proximal trisomy 1q in a girl with developmental delay and minor anomalies.
Furforo L; Rittler M; Slavutsky IR
Am J Med Genet; 1996 Sep; 64(4):551-5. PubMed ID: 8870921
[TBL] [Abstract][Full Text] [Related]
4. [Ocular defects associated with a duplication of the distal part of the long arm of chromosome 1: a case report].
Le Goff L; Hadjadj E; Denis D
J Fr Ophtalmol; 2002 Apr; 25(4):388-92. PubMed ID: 12011743
[TBL] [Abstract][Full Text] [Related]
5. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.
Zneimer SM; Ziel B; Bachman R
Am J Med Genet; 1998 Nov; 80(2):133-5. PubMed ID: 9805129
[TBL] [Abstract][Full Text] [Related]
8. Bilateral perisylvian polymicrogyria and chromosome 1 anomaly.
Ribeiro Mdo C; Gama de Sousa S; Freitas MM; Carrilho I; Fernandes I
Pediatr Neurol; 2007 Jun; 36(6):418-20. PubMed ID: 17560507
[TBL] [Abstract][Full Text] [Related]
9. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
[TBL] [Abstract][Full Text] [Related]
10. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15].
Fechtrup B; Kalhoff H; Diekmann L; Fritz B
Klin Padiatr; 2000; 212(1):35-40. PubMed ID: 10719682
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
[TBL] [Abstract][Full Text] [Related]
12. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
[TBL] [Abstract][Full Text] [Related]
13. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
15. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
[TBL] [Abstract][Full Text] [Related]
16. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
[TBL] [Abstract][Full Text] [Related]
17. Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patient.
Basaran SY; Sensoy V; Kiroglu K; Messiaen L; Tuysuz B
Genet Couns; 2010; 21(3):307-16. PubMed ID: 20964122
[TBL] [Abstract][Full Text] [Related]
18. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
[TBL] [Abstract][Full Text] [Related]
19. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
20. A new case of pure partial 7q duplication.
Alfonsi M; Palka C; Morizio E; Gatta V; Franchi S; Guanciali Franchi P; Zori R; Calabrese G; Palka G; Chiarelli F
Cytogenet Genome Res; 2012; 136(1):1-5. PubMed ID: 22086126
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]