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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 15811006)

  • 1. Calibration of 6q subtelomere deletions to define genotype/phenotype correlations.
    Eash D; Waggoner D; Chung J; Stevenson D; Martin CL
    Clin Genet; 2005 May; 67(5):396-403. PubMed ID: 15811006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.
    Béri-Deixheimer M; Gregoire MJ; Toutain A; Brochet K; Briault S; Schaff JL; Leheup B; Jonveaux P
    Eur J Hum Genet; 2007 Apr; 15(4):446-52. PubMed ID: 17290276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The 6p subtelomere deletion syndrome.
    DeScipio C
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):377-82. PubMed ID: 17918735
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.
    Kok K; Dijkhuizen T; Swart YE; Zorgdrager H; van der Vlies P; Fehrmann R; te Meerman GJ; Gerssen-Schoorl KB; van Essen T; Sikkema-Raddatz B; Buys CH
    Eur J Med Genet; 2005; 48(3):250-62. PubMed ID: 16179221
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.
    Lorda-Sanchez I; Lopez-Pajares I; Roche MC; Sanz R; Rodriguez de Alba M; Gonzalez-Gonzalez MC; Ibañez A; Ramos C; Ayuso C
    Am J Med Genet; 2000 Dec; 95(4):336-8. PubMed ID: 11186887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Subtelomeric imbalances in phenotypically normal individuals.
    Balikova I; Menten B; de Ravel T; Le Caignec C; Thienpont B; Urbina M; Doco-Fenzy M; de Rademaeker M; Mortier G; Kooy F; van den Ende J; Devriendt K; Fryns JP; Speleman F; Vermeesch JR
    Hum Mutat; 2007 Oct; 28(10):958-67. PubMed ID: 17492636
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.
    Ravnan JB; Tepperberg JH; Papenhausen P; Lamb AN; Hedrick J; Eash D; Ledbetter DH; Martin CL
    J Med Genet; 2006 Jun; 43(6):478-89. PubMed ID: 16199540
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
    Baroncini A; Rivieri F; Capucci A; Croci G; Franchi F; Sensi A; Battaglia P; Aiello V; Calzolari E
    Eur J Med Genet; 2005; 48(4):388-96. PubMed ID: 16378923
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
    Kleefstra T; van Zelst-Stams WA; Nillesen WM; Cormier-Daire V; Houge G; Foulds N; van Dooren M; Willemsen MH; Pfundt R; Turner A; Wilson M; McGaughran J; Rauch A; Zenker M; Adam MP; Innes M; Davies C; López AG; Casalone R; Weber A; Brueton LA; Navarro AD; Bralo MP; Venselaar H; Stegmann SP; Yntema HG; van Bokhoven H; Brunner HG
    J Med Genet; 2009 Sep; 46(9):598-606. PubMed ID: 19264732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.
    Klein OD; Cotter PD; Moore MW; Zanko A; Gilats M; Epstein CJ; Conte F; Rauen KA
    Clin Genet; 2007 Mar; 71(3):260-6. PubMed ID: 17309649
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
    Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
    Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interstitial 6q deletion: clinical and array CGH characterisation of a new patient.
    Le Caignec C; Swillen A; Van Asche E; Fryns JP; Vermeesch JR
    Eur J Med Genet; 2005; 48(3):339-45. PubMed ID: 16179229
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA).
    Rooms L; Reyniers E; van Luijk R; Scheers S; Wauters J; Ceulemans B; Van Den Ende J; Van Bever Y; Kooy RF
    Hum Mutat; 2004 Jan; 23(1):17-21. PubMed ID: 14695528
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre.
    Ahn JW; Ogilvie CM; Welch A; Thomas H; Madula R; Hills A; Donaghue C; Mann K
    BMC Med Genet; 2007 Mar; 8():9. PubMed ID: 17338807
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.
    Rauch A; Zink S; Zweier C; Thiel CT; Koch A; Rauch R; Lascorz J; Hüffmeier U; Weyand M; Singer H; Hofbeck M
    J Med Genet; 2005 Nov; 42(11):871-6. PubMed ID: 15831592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.