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 *

121 related articles for article (PubMed ID: 18988819)

  • 41. Battle of the sexes may set the brain.
    Badcock C; Crespi B
    Nature; 2008 Aug; 454(7208):1054-5. PubMed ID: 18756240
    [No Abstract]   [Full Text] [Related]  

  • 42. Common inversion polymorphisms and rare microdeletions at 15q13.3.
    Makoff A; Flomen R
    Eur J Hum Genet; 2009 Feb; 17(2):149-50. PubMed ID: 18854863
    [No Abstract]   [Full Text] [Related]  

  • 43. A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.
    Garcias Gde L; Roth Mda G
    Int J Neurosci; 2007 Jul; 117(7):927-33. PubMed ID: 17613106
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Evolutionary genetics. Are humans still evolving?
    Balter M
    Science; 2005 Jul; 309(5732):234-7. PubMed ID: 16002593
    [No Abstract]   [Full Text] [Related]  

  • 45. 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]  

  • 46. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
    Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS
    Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits.
    Stankiewicz P; Inoue K; Bi W; Walz K; Park SS; Kurotaki N; Shaw CJ; Fonseca P; Yan J; Lee JA; Khajavi M; Lupski JR
    Cold Spring Harb Symp Quant Biol; 2003; 68():445-54. PubMed ID: 15338647
    [No Abstract]   [Full Text] [Related]  

  • 48. Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.
    Lespinasse J; Gimelli S; Béna F; Antonarakis SE; Ansermet F; Paoloni-Giacobino A
    Eur J Med Genet; 2009; 52(1):49-52. PubMed ID: 18992376
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 1.6Mb deletion in chromosome band 3q29 associated with eye abnormalities.
    Tyshchenko N; Hackmann K; Gerlach EM; Neuhann T; Schrock E; Tinschert S
    Eur J Med Genet; 2009; 52(2-3):128-30. PubMed ID: 19298871
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [The application and significance in prenatal diagnosis using G-banding, fluorescence in situ hybridization and comparative genomic hybridization].
    Zhang WS; Chen QN; Wu XH; Liang QH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):156-60. PubMed ID: 19350506
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Diagnosis of Birt-Hogg-Dube syndrome in a patient with spontaneous pneumothorax.
    Pittet O; Christodoulou M; Staneczek O; Ris HB
    Ann Thorac Surg; 2006 Sep; 82(3):1123-5. PubMed ID: 16928562
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Complete Agenesis of the Dorsal Pancreas as a Rare Manifestation of a Chromosomal Anomaly: A Case Report.
    Bogovic OJ; Foufa K; Maniatis V
    Pancreas; 2020 Oct; 49(9):e90-e91. PubMed ID: 33003097
    [No Abstract]   [Full Text] [Related]  

  • 53. 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]  

  • 54. Genetic flux between h1 and h2 haplotypes of the 17q21.31 inversion in European population.
    Deng L; Tang X; Hao X; Chen W; Lin J; Yu Y; Zhang D; Zeng C
    Genomics Proteomics Bioinformatics; 2011 Jun; 9(3):113-8. PubMed ID: 21802048
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human height.
    Buysse K; Reardon W; Mehta L; Costa T; Fagerstrom C; Kingsbury DJ; Anadiotis G; McGillivray BC; Hellemans J; de Leeuw N; de Vries BB; Speleman F; Menten B; Mortier G
    Eur J Med Genet; 2009; 52(2-3):101-7. PubMed ID: 19298872
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Clinical and genetic aspects of 22q13.3 deletion syndrome].
    Gomez-Lado C; Eiris-Punal J; Ansede A; Castro-Gago M
    Rev Neurol; 2007 Sep 16-30; 45(6):379-81. PubMed ID: 17899522
    [No Abstract]   [Full Text] [Related]  

  • 58. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents.
    Knijnenburg J; Oberstein SA; Frei K; Lucas T; Gijsbers AC; Ruivenkamp CA; Tanke HJ; Szuhai K
    J Med Genet; 2009 Jun; 46(6):412-7. PubMed ID: 19246478
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A common inversion under selection in Europeans.
    Stefansson H; Helgason A; Thorleifsson G; Steinthorsdottir V; Masson G; Barnard J; Baker A; Jonasdottir A; Ingason A; Gudnadottir VG; Desnica N; Hicks A; Gylfason A; Gudbjartsson DF; Jonsdottir GM; Sainz J; Agnarsson K; Birgisdottir B; Ghosh S; Olafsdottir A; Cazier JB; Kristjansson K; Frigge ML; Thorgeirsson TE; Gulcher JR; Kong A; Stefansson K
    Nat Genet; 2005 Feb; 37(2):129-37. PubMed ID: 15654335
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical and molecular characterization of two patients with a 6.75 Mb overlapping deletion in 8p12p21 with two candidate loci for congenital heart defects.
    Willemsen MH; de Leeuw N; Pfundt R; de Vries BB; Kleefstra T
    Eur J Med Genet; 2009; 52(2-3):134-9. PubMed ID: 19303465
    [TBL] [Abstract][Full Text] [Related]  

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