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 *

398 related articles for article (PubMed ID: 20643313)

  • 41. Epigenetic factors and autism spectrum disorders.
    Flashner BM; Russo ME; Boileau JE; Leong DW; Gallicano GI
    Neuromolecular Med; 2013 Jun; 15(2):339-50. PubMed ID: 23468062
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
    Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome.
    Lintas C; Sacco R; Persico AM
    Neurobiol Dis; 2012 Jan; 45(1):57-68. PubMed ID: 21130877
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.
    Velinov M; Gu H; Genovese M; Duncan C; Brown WT; Jenkins E
    Mol Genet Metab; 2000 Jan; 69(1):81-3. PubMed ID: 10655162
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Genomic imprinting in the development and evolution of psychotic spectrum conditions.
    Crespi B
    Biol Rev Camb Philos Soc; 2008 Nov; 83(4):441-93. PubMed ID: 18783362
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Genetics and epigenetics in autism].
    Nakayama A; Masaki S; Aoki E
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2006 Nov; 26(5-6):209-12. PubMed ID: 17240846
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Epigenetics' implication in autism spectrum disorders: A review].
    Hamza M; Halayem S; Mrad R; Bourgou S; Charfi F; Belhadj A
    Encephale; 2017 Aug; 43(4):374-381. PubMed ID: 27692350
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.
    Betancur C
    Brain Res; 2011 Mar; 1380():42-77. PubMed ID: 21129364
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Childhood and adolescent anxiety and depression: beyond heritability.
    Franić S; Middeldorp CM; Dolan CV; Ligthart L; Boomsma DI
    J Am Acad Child Adolesc Psychiatry; 2010 Aug; 49(8):820-9. PubMed ID: 20643315
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A new genetic test for Prader-Willi and Angelman syndromes.
    Lovell-Smith CJ; Watt AJ; Gardner RJ
    N Z Med J; 1995 May; 108(999):179. PubMed ID: 7753521
    [No Abstract]   [Full Text] [Related]  

  • 53. Common genetic and epigenetic syndromes.
    Adams DJ; Clark DA
    Pediatr Clin North Am; 2015 Apr; 62(2):411-26. PubMed ID: 25836705
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Brief report: visual-spatial deficit in a 16-year-old girl with maternally derived duplication of proximal 15q.
    Cohen D; Martel C; Wilson A; Déchambre N; Amy C; Duverger L; Guile JM; Pipiras E; Benzacken B; Cavé H; Cohen L; Héron D; Plaza M
    J Autism Dev Disord; 2007 Sep; 37(8):1585-91. PubMed ID: 17006777
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA
    Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.
    Knoll JH; Wagstaff J; Lalande M
    Am J Med Genet; 1993 Apr; 46(1):2-6. PubMed ID: 8388170
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
    Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
    Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
    [TBL] [Abstract][Full Text] [Related]  

  • 58. RPP25 is developmentally regulated in prefrontal cortex and expressed at decreased levels in autism spectrum disorder.
    Huang HS; Cheung I; Akbarian S
    Autism Res; 2010 Aug; 3(4):153-61. PubMed ID: 20632321
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status.
    Ellaway C; Buchholz T; Smith A; Leonard H; Christodoulou J
    J Child Neurol; 1998 Sep; 13(9):448-51. PubMed ID: 9733292
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Cytogenetic diagnosis of genetic diseases.
    Shapiro LR; Wilmot PL
    Pediatr Ann; 1993 May; 22(5):298-303. PubMed ID: 8510996
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.