360 related articles for article (PubMed ID: 18990980)
1. De novo 18q deletion with mitral valve insufficiency.
Gunes S; Okten G; Kara N; Saglam Y; Tasdemir HA; Kayacik OE; Tural S
Genet Couns; 2008; 19(3):261-5. PubMed ID: 18990980
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
[TBL] [Abstract][Full Text] [Related]
3. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
4. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
[TBL] [Abstract][Full Text] [Related]
5. Direct transmission of the 18q- syndrome from mother to daughter.
Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W
Genet Couns; 2006; 17(2):185-9. PubMed ID: 16970036
[TBL] [Abstract][Full Text] [Related]
6. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
[No Abstract] [Full Text] [Related]
7. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).
Gustavsson P; Kimber E; Wahlström J; Annerén G
Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171
[TBL] [Abstract][Full Text] [Related]
8. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
9. 18q- and 18q+ mosaicism in a mentally retarded boy.
Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
[TBL] [Abstract][Full Text] [Related]
10. Familial deletion of chromosome 18 (p11.2).
Velagaleti GV; Harris S; Carpenter NJ; Coldwell J; Say B
Ann Genet; 1996; 39(4):201-4. PubMed ID: 9037347
[TBL] [Abstract][Full Text] [Related]
11. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
[TBL] [Abstract][Full Text] [Related]
12. Mild mental retardation in a child with a de novo interstitial deletion of 15q21.2q22.1: a comparison with previously described cases.
Tempesta S; Sollima D; Ghezzo S; Politi V; Sinigaglia B; Balducci F; Celso B; Restuccia A; Stefani M; Cernetti R; Marzocchi C; Ciccone R; Zuffardi O; Bovicelli L; Santarini L
Eur J Med Genet; 2008; 51(6):639-45. PubMed ID: 18757045
[TBL] [Abstract][Full Text] [Related]
13. Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry.
Cooke A; Tolmie JL; Glencross FJ; Boyd E; Clarke MM; Day R; Stephenson JB; Connor JM
Am J Med Genet; 1989 Apr; 32(4):545-9. PubMed ID: 2774001
[TBL] [Abstract][Full Text] [Related]
14. Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18.
de Pater JM; Poot M; Beemer FA; Bijlsma JB; Hack WW; Van Dam WM; Eleveld MJ; Loneus WH; Engelen JJ
Eur J Med Genet; 2006; 49(1):19-27. PubMed ID: 16473306
[TBL] [Abstract][Full Text] [Related]
15. Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
Kitsiou-Tzeli S; Sismani C; Ioannides M; Bashiardes S; Ketoni A; Touliatou V; Kolialexi A; Mavrou A; Kanavakis E; Patsalis PC
Eur J Med Genet; 2007; 50(1):73-8. PubMed ID: 17194633
[TBL] [Abstract][Full Text] [Related]
16. Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.
Riegel M; Hargreaves P; Baumer A; Guc-Scekic M; Ignjatovic M; Schinzel A
Eur J Med Genet; 2005; 48(2):167-74. PubMed ID: 16053908
[TBL] [Abstract][Full Text] [Related]
17. Dystonia in a patient with deletion of 18q.
Gordon MF; Bressman S; Brin MF; de Leon D; Warburton D; Yeboa K; Fahn S
Mov Disord; 1995 Jul; 10(4):496-9. PubMed ID: 7565832
[TBL] [Abstract][Full Text] [Related]
18. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
[TBL] [Abstract][Full Text] [Related]
19. Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.
Abu-Amero KK; Hellani A; Salih MA; Alorainy IA; Zidan G; Kern KC; Sicotte NL; Bosley TM
Ophthalmic Genet; 2010 Sep; 31(3):147-54. PubMed ID: 20565246
[TBL] [Abstract][Full Text] [Related]
20. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
