79 related articles for article (PubMed ID: 20807304)
21. Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.
Joyce CA; Dennis NR; Cooper S; Browne CE
Hum Genet; 2001 Oct; 109(4):440-51. PubMed ID: 11702226
[TBL] [Abstract][Full Text] [Related]
22. Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.
Saugier-Veber P; Goldenberg A; Drouin-Garraud V; de La Rochebrochard C; Layet V; Drouot N; Le Meur N; Gilbert-Du-Ssardier B; Joly-Hélas G; Moirot H; Rossi A; Tosi M; Frébourg T
Eur J Hum Genet; 2006 Sep; 14(9):1009-17. PubMed ID: 16773131
[TBL] [Abstract][Full Text] [Related]
23. Copy-number variations associated with neuropsychiatric conditions.
Cook EH; Scherer SW
Nature; 2008 Oct; 455(7215):919-23. PubMed ID: 18923514
[TBL] [Abstract][Full Text] [Related]
24. Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.
Rooms L; Reyniers E; Kooy RF
Hum Mutat; 2007 Feb; 28(2):177-82. PubMed ID: 16991117
[TBL] [Abstract][Full Text] [Related]
25. Clinical and cytogenetic manifestations of subtelomeric aberrations: Report of six cases.
Font-Montgomery E; Weaver DD; Walsh L; Christensen C; Thurston VC
Birth Defects Res A Clin Mol Teratol; 2004 Jun; 70(6):408-15. PubMed ID: 15211711
[TBL] [Abstract][Full Text] [Related]
26. Mental retardation in Down syndrome: from gene dosage imbalance to molecular and cellular mechanisms.
Rachidi M; Lopes C
Neurosci Res; 2007 Dec; 59(4):349-69. PubMed ID: 17897742
[TBL] [Abstract][Full Text] [Related]
27. Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.
Rooms L; Reyniers E; Wuyts W; Storm K; van Luijk R; Scheers S; Wauters J; van den Ende J; Biervliet M; Eyskens F; van Goethem G; Laridon A; Ceulemans B; Courtens W; Kooy RF
Clin Genet; 2006 Jan; 69(1):58-64. PubMed ID: 16451137
[TBL] [Abstract][Full Text] [Related]
28. Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.
Bocian E; Hélias-Rodzewicz Z; Suchenek K; Obersztyn E; Kutkowska-Kaźmierczak A; Stankiewicz P; Kostyk E; Mazurczak T
Med Sci Monit; 2004 Apr; 10(4):CR143-51. PubMed ID: 15039644
[TBL] [Abstract][Full Text] [Related]
29. Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.
Mihçi E; Ozcan M; Berker-Karaüzüm S; Keser I; Taçoy S; Hapsolat S; Lüleci G
Turk J Pediatr; 2009; 51(5):453-9. PubMed ID: 20112600
[TBL] [Abstract][Full Text] [Related]
30. High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardation.
Lam AC; Lam ST; Lai KK; Tong TM; Chau TC
Clin Biochem; 2006 Mar; 39(3):196-202. PubMed ID: 16497288
[TBL] [Abstract][Full Text] [Related]
31. Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres.
Slavotinek A; Rosenberg M; Knight S; Gaunt L; Fergusson W; Killoran C; Clayton-Smith J; Kingston H; Campbell RH; Flint J; Donnai D; Biesecker L
J Med Genet; 1999 May; 36(5):405-11. PubMed ID: 10353788
[TBL] [Abstract][Full Text] [Related]
32. What a difference copy number variation makes.
Kehrer-Sawatzki H
Bioessays; 2007 Apr; 29(4):311-3. PubMed ID: 17373652
[TBL] [Abstract][Full Text] [Related]
33. Human subtelomeric copy number variations.
Riethman H
Cytogenet Genome Res; 2008; 123(1-4):244-52. PubMed ID: 19287161
[TBL] [Abstract][Full Text] [Related]
34. Familial mental retardation due to a cryptic subtelomeric translocation -del 14qter and dup 9qter (the Anyon phenotype).
Lowry RB; Baker E; Dixon J; Hinton L
Clin Dysmorphol; 2007 Oct; 16(4):223-9. PubMed ID: 17786113
[TBL] [Abstract][Full Text] [Related]
35. Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the myelin transcription factor 1 gene (MYT1).
Kroepfl T; Petek E; Schwarzbraun T; Kroisel PM; Plecko B
Clin Genet; 2008 May; 73(5):492-5. PubMed ID: 18341605
[TBL] [Abstract][Full Text] [Related]
36. [Detection of subtelomeric copy number variations in children with intellectual disability].
Zhu LN; Wang Y; Peng W; Ma XW; Yang X; Liu X; Feng ZC
Zhongguo Dang Dai Er Ke Za Zhi; 2015 Dec; 17(12):1273-6. PubMed ID: 26695663
[TBL] [Abstract][Full Text] [Related]
37. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
Boehm D; Herold S; Kuechler A; Liehr T; Laccone F
Hum Mutat; 2004 Apr; 23(4):368-78. PubMed ID: 15024731
[TBL] [Abstract][Full Text] [Related]
38. Genome structural variation and sporadic disease traits.
Lupski JR
Nat Genet; 2006 Sep; 38(9):974-6. PubMed ID: 16941003
[No Abstract] [Full Text] [Related]
39. Genome rearrangements in patients with blepharophimosis, mental retardation and hypothyroidism, so-called Young-Simpson syndrome.
Brancati F; Bernardini L; Cavalcanti DP; Romano C; Novelli A; Dallapiccola B
Clin Genet; 2009 Aug; 76(2):210-3. PubMed ID: 19659891
[No Abstract] [Full Text] [Related]
40. Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
Sismani C; Armour JA; Flint J; Girgalli C; Regan R; Patsalis PC
Eur J Hum Genet; 2001 Jul; 9(7):527-32. PubMed ID: 11464244
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]