108 related articles for article (PubMed ID: 11394378)
1. 16q subtelomeric deletion in proband with congenital malformations and mental retardation.
Vorsanova SG; Yurov YB; Kolotii AD; Demidova IA; Novikova IM
Tsitol Genet; 2000; 34(6):72-4. PubMed ID: 11394378
[TBL] [Abstract][Full Text] [Related]
2. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
3. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
[TBL] [Abstract][Full Text] [Related]
4. Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.
Cogulu O; Gunduz C; Karaca E; Onay H; Ozkinay C; Ozkinay F
Genet Couns; 2006; 17(3):321-31. PubMed ID: 17100201
[TBL] [Abstract][Full Text] [Related]
5. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.
Flint J; Wilkie AO; Buckle VJ; Winter RM; Holland AJ; McDermid HE
Nat Genet; 1995 Feb; 9(2):132-40. PubMed ID: 7719339
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
[TBL] [Abstract][Full Text] [Related]
8. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
Ballif BC; Kashork CD; Shaffer LG
Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
[TBL] [Abstract][Full Text] [Related]
11. Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
Koolen DA; Nillesen WM; Versteeg MH; Merkx GF; Knoers NV; Kets M; Vermeer S; van Ravenswaaij CM; de Kovel CG; Brunner HG; Smeets D; de Vries BB; Sistermans EA
J Med Genet; 2004 Dec; 41(12):892-9. PubMed ID: 15591274
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
[TBL] [Abstract][Full Text] [Related]
14. A patient with 13q-syndrome with mild mental retardation and with growth retardation.
Stoll C; Alembik Y
Ann Genet; 1998; 41(4):209-12. PubMed ID: 9881184
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation.
Kulikowski LD; Yoshimoto M; da Silva Bellucco FT; Belangero SI; Christofolini DM; Pacanaro AN; Bortolai A; Smith Mde A; Squire JA; Melaragno MI
Eur J Med Genet; 2010; 53(6):404-7. PubMed ID: 20837174
[TBL] [Abstract][Full Text] [Related]
20. Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.
Maserati E; Verri A; Seghezzi L; Tupler R; Federico A; Tiepolo L; Maraschio P
Ann Genet; 1999; 42(4):210-4. PubMed ID: 10674160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
