BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

373 related articles for article (PubMed ID: 17309649)

  • 1. 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]  

  • 2. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Narrowing the deleted region associated with the 15q21 syndrome.
    Pramparo T; Mattina T; Gimelli S; Liehr T; Zuffardi O
    Eur J Med Genet; 2005; 48(3):346-52. PubMed ID: 16179230
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
    Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
    Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA; Albertson DG; Pinkel D; Cotter PD
    Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. An emerging phenotype of proximal 11q deletions.
    Melis D; Genesio R; Cozzolino M; Del Giudice E; Mormile A; Imperati F; Ronga V; Della Casa R; Nitsch L; Andria G
    Eur J Med Genet; 2010; 53(5):340-3. PubMed ID: 20688202
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
    Bosga-Bouwer AG; Kok K; Booman M; Boven L; van der Vlies P; van den Berg A; van den Berg E; de Jong B; Poppema S; Kluin P
    Genes Chromosomes Cancer; 2006 Oct; 45(10):976-81. PubMed ID: 16865685
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.
    Mantripragada KK; Buckley PG; Benetkiewicz M; De Bustos C; Hirvelä C; Jarbo C; Bruder CE; Wensman H; Mathiesen T; Nyberg G; Papi L; Collins VP; Ichimura K; Evans G; Dumanski JP
    Int J Oncol; 2003 Mar; 22(3):615-22. PubMed ID: 12579316
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
    Davidsson J; Collin A; Olsson ME; Lundgren J; Soller M
    Epilepsy Res; 2008 Sep; 81(1):69-79. PubMed ID: 18539002
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to approximately 650 kb.
    Schoumans J; Staaf J; Jönsson G; Rantala J; Zimmer KS; Borg A; Nordenskjöld M; Anderlid BM
    Eur J Med Genet; 2005; 48(3):290-300. PubMed ID: 16179224
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
    Nagamani SC; Zhang F; Shchelochkov OA; Bi W; Ou Z; Scaglia F; Probst FJ; Shinawi M; Eng C; Hunter JV; Sparagana S; Lagoe E; Fong CT; Pearson M; Doco-Fenzy M; Landais E; Mozelle M; Chinault AC; Patel A; Bacino CA; Sahoo T; Kang SH; Cheung SW; Lupski JR; Stankiewicz P
    J Med Genet; 2009 Dec; 46(12):825-33. PubMed ID: 19584063
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay.
    Andrieux J; Richebourg S; Duban-Bedu B; Petit F; Leprêtre F; Sukno S; Dehouck MB; Delobel B
    Eur J Med Genet; 2008; 51(4):373-81. PubMed ID: 18463015
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.
    Rea G; McCullough S; McNerlan S; Craig B; Morrison PJ
    Eur J Med Genet; 2010; 53(3):162-7. PubMed ID: 20215058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
    Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
    Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH).
    Maas NM; Van Buggenhout G; Hannes F; Thienpont B; Sanlaville D; Kok K; Midro A; Andrieux J; Anderlid BM; Schoumans J; Hordijk R; Devriendt K; Fryns JP; Vermeesch JR
    J Med Genet; 2008 Feb; 45(2):71-80. PubMed ID: 17873117
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.