These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
450 related articles for article (PubMed ID: 15904506)
1. Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter. Sogaard M; Tümer Z; Hjalgrim H; Hahnemann J; Friis B; Ledaal P; Pedersen VF; Baekgaard P; Tommerup N; Cingöz S; Duno M; Brondum-Nielsen K BMC Med Genet; 2005 May; 6():21. PubMed ID: 15904506 [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. Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods. Erjavec-Skerget A; Stangler-Herodez S; Zagorac A; Zagradisnik B; Kokalj-Vokac N Croat Med J; 2006 Dec; 47(6):841-50. PubMed ID: 17167856 [TBL] [Abstract][Full Text] [Related]
4. Subtelomeric fish findings in Turkish patients with idiopathic mental retardation. Tos T; Vurucu S; Karkucak M; Kozan S; Gul D; Akin R Genet Couns; 2013; 24(3):259-64. PubMed ID: 24341139 [TBL] [Abstract][Full Text] [Related]
5. [Cytogenetic-molecular analysis of balanced chromosomal rearrangements in nine patients with intellectual disability, dysmorphic features and congenital abnormalities]. Borg K; Bocian E; Stankiewicz P; Obersztyn E; Kruczek A; Nowakowska B; Ilnicka A; Mazurczak T Med Wieku Rozwoj; 2006; 10(1 Pt 2):227-46. PubMed ID: 17028391 [TBL] [Abstract][Full Text] [Related]
6. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay. Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233 [TBL] [Abstract][Full Text] [Related]
8. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features. Debost-Legrand A; Capri Y; Gouas L; Pebrel-Richard C; Veronese L; Tchirkov A; Haoud K; Boespflug-Tanguy O; Goumy C; Vago P Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667 [TBL] [Abstract][Full Text] [Related]
9. Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patients. Tos T; Karaman A; Aksoy A; Tukun A Genet Couns; 2012; 23(2):289-96. PubMed ID: 22876589 [TBL] [Abstract][Full Text] [Related]
10. 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]
12. 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]
13. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases. Shao L; Shaw CA; Lu XY; Sahoo T; Bacino CA; Lalani SR; Stankiewicz P; Yatsenko SA; Li Y; Neill S; Pursley AN; Chinault AC; Patel A; Beaudet AL; Lupski JR; Cheung SW Am J Med Genet A; 2008 Sep; 146A(17):2242-51. PubMed ID: 18663743 [TBL] [Abstract][Full Text] [Related]
14. Subtelomeric rearrangements detected by FISH in three of 33 families with idiopathic mental retardation and minor physical anomalies. Hélias-Rodzewicz Z; Bocian E; Stankiewicz P; Obersztyn E; Kostyk E; Jakubów-Durska K; Kutkowska-Kaźmierczak A; Mazurczak T J Med Genet; 2002 Sep; 39(9):e53. PubMed ID: 12205123 [No Abstract] [Full Text] [Related]
15. 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]
16. [Subtelomeric aberration as a cause of severe somatic and psychomotor retardation in a child with dysmorphic features and CNS defects]. Kutkowska-Kaźmierczak A; Obersztyn E; Helias-Rodzewicz Z; Bocian E; Mazurczak T Med Wieku Rozwoj; 2004; 8(4 Pt 1):949-62. PubMed ID: 15951614 [TBL] [Abstract][Full Text] [Related]
17. Subtelomeric rearrangements detected in patients with idiopathic mental retardation. Anderlid BM; Schoumans J; Annerén G; Sahlén S; Kyllerman M; Vujic M; Hagberg B; Blennow E; Nordenskjöld M Am J Med Genet; 2002 Feb; 107(4):275-84. PubMed ID: 11840483 [TBL] [Abstract][Full Text] [Related]
18. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist. de Vries BB; White SM; Knight SJ; Regan R; Homfray T; Young ID; Super M; McKeown C; Splitt M; Quarrell OW; Trainer AH; Niermeijer MF; Malcolm S; Flint J; Hurst JA; Winter RM J Med Genet; 2001 Mar; 38(3):145-50. PubMed ID: 11238680 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]