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 *

138 related articles for article (PubMed ID: 18698619)

  • 21. 13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation.
    Struski S; Helias C; Gervais C; Audhuy B; Zamfir A; Herbrecht R; Lessard M
    Cancer Genet Cytogenet; 2007 Apr; 174(2):151-60. PubMed ID: 17452258
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array-based comparative genomic hybridization.
    Hayashi S; Ono M; Makita Y; Imoto I; Mizutani S; Inazawa J
    Am J Med Genet A; 2007 Jun; 143A(11):1191-7. PubMed ID: 17497725
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3.
    Garcia-Miñaur S; Ramsay J; Grace E; Minns RA; Myles LM; FitzPatrick DR
    Am J Med Genet A; 2005 Feb; 132A(4):402-10. PubMed ID: 15742475
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
    Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
    Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
    [TBL] [Abstract][Full Text] [Related]  

  • 25. FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications.
    Gentile M; Di Carlo A; Volpe P; Pansini A; Nanna P; Valenzano MC; Buonadonna AL
    Am J Med Genet A; 2003 Mar; 117A(3):251-4. PubMed ID: 12599188
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man.
    Hannachi H; Mougou-Zerelli S; BenAbdallah I; Mama N; Hamdi I; Labalme A; Elghezal H; Sanlaville D; Saad A
    Cytogenet Genome Res; 2011; 135(2):102-10. PubMed ID: 21876345
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A de novo 4q34 interstitial deletion of at least 9.3 Mb with no discernible phenotypic effect.
    Bateman MS; Mehta SG; Willatt L; Selkirk E; Bedwell C; Zwolinski S; Sparnon L; Simonic I; Abbott K; Barber JC
    Am J Med Genet A; 2010 Jul; 152A(7):1764-9. PubMed ID: 20583179
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.
    Quélin C; Bendavid C; Dubourg C; de la Rochebrochard C; Lucas J; Henry C; Jaillard S; Loget P; Loeuillet L; Lacombe D; Rival JM; David V; Odent S; Pasquier L
    Eur J Med Genet; 2009; 52(1):41-6. PubMed ID: 19022413
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.
    Guediche N; Tosca L; Nouchy M; Lecerf L; Cornet D; Brisset S; Goossens M; Tachdjian G
    Eur J Med Genet; 2012 Dec; 55(12):737-42. PubMed ID: 23017438
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.
    Vona B; Nanda I; Neuner C; Schröder J; Kalscheuer VM; Shehata-Dieler W; Haaf T
    BMC Med Genet; 2014 Jun; 15():72. PubMed ID: 24962056
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
    Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chromosome deletions in 13q33-34: report of four patients and review of the literature.
    Walczak-Sztulpa J; Wisniewska M; Latos-Bielenska A; Linné M; Kelbova C; Belitz B; Pfeiffer L; Kalscheuer V; Erdogan F; Kuss AW; Ropers HH; Ullmann R; Tzschach A
    Am J Med Genet A; 2008 Feb; 146A(3):337-42. PubMed ID: 18203171
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Partial monosomy of 10p and duplication of another chromosome in two patients.
    Ohta S; Isojima T; Mizuno Y; Kato M; Mimaki M; Seki M; Sato Y; Ogawa S; Takita J; Kitanaka S; Oka A
    Pediatr Int; 2017 Jan; 59(1):99-102. PubMed ID: 28102624
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.
    Kulharya AS; Flannery DB; Norris K; Lovell C; Levy B; Velagaleti GV
    Am J Med Genet A; 2008 Sep; 146A(17):2234-41. PubMed ID: 18666229
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal reflux.
    Champaigne NL; Laird NA; Northup JK; Velagaleti GV
    Am J Med Genet A; 2009 Feb; 149A(4):751-4. PubMed ID: 19291769
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
    Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
    Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Xp contiguous deletion syndrome and autism.
    Shinawi M; Patel A; Panichkul P; Zascavage R; Peters SU; Scaglia F
    Am J Med Genet A; 2009 Jun; 149A(6):1138-48. PubMed ID: 19441126
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy.
    Fonseca R; Oken MM; Harrington D; Bailey RJ; Van Wier SA; Henderson KJ; Kay NE; Van Ness B; Greipp PR; Dewald GW
    Leukemia; 2001 Jun; 15(6):981-6. PubMed ID: 11417487
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
    Fernandez TV; García-González IJ; Mason CE; Hernández-Zaragoza G; Ledezma-Rodríguez VC; Anguiano-Alvarez VM; E'Vega R; Gutiérrez-Angulo M; Maya ML; García-Bejarano HE; González-Cruz M; Barrios S; Atorga R; López-Cardona MG; Armendariz-Borunda J; State MW; Dávalos NO
    Am J Med Genet A; 2008 Nov; 146A(21):2746-52. PubMed ID: 18837054
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.