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 *

127 related articles for article (PubMed ID: 17486614)

  • 21. 18q deletions: clinical, molecular, and brain MRI findings of 14 individuals.
    Linnankivi T; Tienari P; Somer M; Kähkönen M; Lönnqvist T; Valanne L; Pihko H
    Am J Med Genet A; 2006 Feb; 140(4):331-9. PubMed ID: 16419126
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development.
    Wilson HL; Crolla JA; Walker D; Artifoni L; Dallapiccola B; Takano T; Vasudevan P; Huang S; Maloney V; Yobb T; Quarrell O; McDermid HE
    Eur J Hum Genet; 2008 Nov; 16(11):1301-10. PubMed ID: 18523453
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome).
    Sarasua SM; Dwivedi A; Boccuto L; Rollins JD; Chen CF; Rogers RC; Phelan K; DuPont BR; Collins JS
    J Med Genet; 2011 Nov; 48(11):761-6. PubMed ID: 21984749
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).
    Gustavsson P; Kimber E; Wahlström J; Annerén G
    Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array.
    Andrieux J; Lepretre F; Cuisset JM; Goldenberg A; Delobel B; Manouvrier-Hanu S; Holder-Espinasse M
    Eur J Med Genet; 2008; 51(2):172-7. PubMed ID: 18222743
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analysis of clinical variation seen in patients with 18q terminal deletions.
    Strathdee G; Zackai EH; Shapiro R; Kamholz J; Overhauser J
    Am J Med Genet; 1995 Dec; 59(4):476-83. PubMed ID: 8585568
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular characterization of 18p deletions: evidence for a breakpoint cluster.
    Schaub RL; Reveles XT; Baillargeon J; Leach RJ; Cody JD
    Genet Med; 2002; 4(1):15-9. PubMed ID: 11839953
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Establishing a reference group for distal 18q-: clinical description and molecular basis.
    Cody JD; Hasi M; Soileau B; Heard P; Carter E; Sebold C; O'Donnell L; Perry B; Stratton RF; Hale DE
    Hum Genet; 2014 Feb; 133(2):199-209. PubMed ID: 24092497
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.
    Stankiewicz P; Brozek I; Hélias-Rodzewicz Z; Wierzba J; Pilch J; Bocian E; Balcerska A; Wozniak A; Kardaś I; Wirth J; Mazurczak T; Limon J
    Am J Med Genet; 2001 Jul; 101(3):226-39. PubMed ID: 11424138
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular analysis redefines three human chromosome 14 deletions.
    Wintle RF; Costa T; Haslam RH; Teshima IE; Cox DW
    Hum Genet; 1995 May; 95(5):495-500. PubMed ID: 7759068
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.
    Koolen DA; Reardon W; Rosser EM; Lacombe D; Hurst JA; Law CJ; Bongers EM; van Ravenswaaij-Arts CM; Leisink MA; van Kessel AG; Veltman JA; de Vries BB
    Eur J Hum Genet; 2005 Sep; 13(9):1019-24. PubMed ID: 15986041
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.
    Estabrooks LL; Lamb AN; Aylsworth AS; Callanan NP; Rao KW
    J Med Genet; 1994 Feb; 31(2):103-7. PubMed ID: 8182713
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
    Shapira SK; McCaskill C; Northrup H; Spikes AS; Elder FF; Sutton VR; Korenberg JR; Greenberg F; Shaffer LG
    Am J Hum Genet; 1997 Sep; 61(3):642-50. PubMed ID: 9326330
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
    Caliebe A; Kroes HY; van der Smagt JJ; Martin-Subero JI; Tönnies H; van 't Slot R; Nievelstein RA; Muhle H; Stephani U; Alfke K; Stefanova I; Hellenbroich Y; Gillessen-Kaesbach G; Hochstenbach R; Siebert R; Poot M
    Eur J Med Genet; 2010; 53(4):179-85. PubMed ID: 20382278
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients.
    Portnoï MF; Gruchy N; Marlin S; Finkel L; Denoyelle F; Dubourg C; Odent S; Siffroi JP; Le Bouc Y; Houang M
    Clin Dysmorphol; 2007 Oct; 16(4):247-52. PubMed ID: 17786116
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
    Heilstedt HA; Ballif BC; Howard LA; Lewis RA; Stal S; Kashork CD; Bacino CA; Shapira SK; Shaffer LG
    Am J Hum Genet; 2003 May; 72(5):1200-12. PubMed ID: 12687501
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Consequences of chromsome18q deletions.
    Cody JD; Sebold C; Heard P; Carter E; Soileau B; Hasi-Zogaj M; Hill A; Rupert D; Perry B; O'Donnell L; Gelfond J; Lancaster J; Fox PT; Hale DE
    Am J Med Genet C Semin Med Genet; 2015 Sep; 169(3):265-80. PubMed ID: 26235940
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
    Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
    J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
    [TBL] [Abstract][Full Text] [Related]  

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