BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

842 related articles for article (PubMed ID: 16433693)

  • 21. The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.
    Urraca N; Cleary J; Brewer V; Pivnick EK; McVicar K; Thibert RL; Schanen NC; Esmer C; Lamport D; Reiter LT
    Autism Res; 2013 Aug; 6(4):268-79. PubMed ID: 23495136
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Evaluation of q11-q13 locus of chromosome 15 aberrations and polymorphisms in the B3 subunit of the GABA-A receptor gene (GABRB3) in autistic patients].
    Słopień A; Rajewski A; Budny B; Czerski P
    Psychiatr Pol; 2002; 36(5):779-91. PubMed ID: 12491987
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B; Hallmayer J; Rogers T; Kalaydjieva L; Petersen PB; Nicholas P; Pingree C; McMahon W; Spiker D; Lotspeich L; Kraemer H; McCague P; Dimiceli S; Nouri N; Pitts T; Yang J; Hinds D; Myers RM; Risch N
    Am J Med Genet; 1999 Oct; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
    Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida.
    Gustavsson P; Schoumans J; Staaf J; Borg A; Nordenskjöld M; Annerén G
    Eur J Med Genet; 2007; 50(3):237-41. PubMed ID: 17387046
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
    Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
    Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Array-based comparative genomic hybridization characterizes a deletion associated with a t(15;17) in acute promyelocytic leukemia.
    Dolan M; Peterson B; Hirsch B
    Am J Clin Pathol; 2008 Nov; 130(5):818-23. PubMed ID: 18854276
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.
    Sutcliffe JS; Nurmi EL; Lombroso PJ
    J Am Acad Child Adolesc Psychiatry; 2003 Feb; 42(2):253-6. PubMed ID: 12544187
    [No Abstract]   [Full Text] [Related]  

  • 30. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
    Cook EH; Lindgren V; Leventhal BL; Courchesne R; Lincoln A; Shulman C; Lord C; Courchesne E
    Am J Hum Genet; 1997 Apr; 60(4):928-34. PubMed ID: 9106540
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA; Kashork CD; Davino NA; Shaffer LG
    Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
    Nurmi EL; Amin T; Olson LM; Jacobs MM; McCauley JL; Lam AY; Organ EL; Folstein SE; Haines JL; Sutcliffe JS
    Mol Psychiatry; 2003 Jun; 8(6):624-34, 570. PubMed ID: 12851639
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
    Maddox LO; Menold MM; Bass MP; Rogala AR; Pericak-Vance MA; Vance JM; Gilbert JR
    Genomics; 1999 Dec; 62(3):325-31. PubMed ID: 10644429
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
    Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
    Dutta UR; Vempally S; Ranganath P; Dalal A
    Gene; 2014 Apr; 539(1):162-7. PubMed ID: 24508374
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 43.