218 related articles for article (PubMed ID: 11140412)
1. Trisomy 7p: report of 2 patients and literature review.
Arens YH; Toutain A; Engelen JJ; Offermans JP; Hamers AJ; Schrander JJ; Pulles-Heintzberger CF; Schrander-Stumpel CT
Genet Couns; 2000; 11(4):347-54. PubMed ID: 11140412
[TBL] [Abstract][Full Text] [Related]
2. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI
Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445
[TBL] [Abstract][Full Text] [Related]
3. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
[TBL] [Abstract][Full Text] [Related]
4. Further delineation of 7p trisomy. Case report and review of literature.
Pallotta R; Dalprà L; Fusilli P; Zuffardi O
Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
Lurie IW; Schwartz MF; Schwartz S; Cohen MM
Am J Med Genet; 1995 Jan; 55(1):62-6. PubMed ID: 7702099
[TBL] [Abstract][Full Text] [Related]
6. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
Plotner PL; Smith JL; Northrup H
Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
[TBL] [Abstract][Full Text] [Related]
7. Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.
Saneto RP; Applegate KE; Frankel DG
Am J Med Genet; 1998 Oct; 80(1):42-5. PubMed ID: 9800910
[TBL] [Abstract][Full Text] [Related]
8. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
12. [A case of partial 6q trisomy diagnosed at birth].
Bartalena L; D'Accavio L; Pellegrinetti C; Tarantino E
Pathologica; 1990; 82(1081):549-52. PubMed ID: 2080100
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
Park JP; McDermet MK; Moeschler JB; Wurster-Hill DH
Ann Genet; 1993; 36(4):217-20. PubMed ID: 8166428
[TBL] [Abstract][Full Text] [Related]
15. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
[TBL] [Abstract][Full Text] [Related]
16. A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration.
Eggermann T; Kolin-Gerresheim I; Gerresheim F; Schwanitz G
Ann Genet; 1998; 41(4):205-8. PubMed ID: 9881183
[TBL] [Abstract][Full Text] [Related]
17. Kabuki syndrome and trisomy 10p.
Utine GE; Alanay Y; Atkaş D; Boduroğlu K; Alikaşifoğlu M; Tunçbilek E
Genet Couns; 2008; 19(3):291-300. PubMed ID: 18990985
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Two sibs with partial trisomy 2q.
Barnicoat AJ; Abusaad I; Mackie CM; Robards MF
Am J Med Genet; 1997 May; 70(2):166-70. PubMed ID: 9128937
[TBL] [Abstract][Full Text] [Related]
20. Distal partial trisomy 1q: report of two cases and a review of the literature.
Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]