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 *

55 related articles for article (PubMed ID: 2353962)

  • 1. Autistic disorder and additional inv dup(15)(pter----q13) chromosome.
    Schinzel A
    Am J Med Genet; 1990 Mar; 35(3):447-8. PubMed ID: 2353962
    [No Abstract]   [Full Text] [Related]  

  • 2. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
    Flejter WL; Bennett-Baker PE; Ghaziuddin M; McDonald M; Sheldon S; Gorski JL
    Am J Med Genet; 1996 Jan; 61(2):182-7. PubMed ID: 8669450
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maternal origin of inv dup(15) chromosomes in infantile autism.
    Martinsson T; Johannesson T; Vujic M; Sjöstedt A; Steffenburg S; Gillberg C; Wahlström J
    Eur Child Adolesc Psychiatry; 1996 Dec; 5(4):185-92. PubMed ID: 8989557
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB; Zackai E; Cheng SD; Knoll JH
    Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inv dup(15): contribution to the clinical definition of phenotype.
    Grammatico P; Di Rosa C; Roccella M; Falcolini M; Pelliccia A; Roccella F; Del Porto G
    Clin Genet; 1994 Sep; 46(3):233-7. PubMed ID: 7820937
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of an extra inv dup(15)(q13) chromosome in two patients with Angelman syndrome.
    Buchholz T; Schuffenhauer S; Evans K; Robson L; Appleton B; Smith A
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):217-20. PubMed ID: 8872034
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. Identification of a marker chromosome as inv dup(15) by molecular analysis.
    Shibuya Y; Tonoki H; Kajii N; Niikawa N
    Clin Genet; 1991 Sep; 40(3):233-6. PubMed ID: 1685358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [West's syndrome associated with inversion duplication of chromosome 15].
    Cabrera JC; Martí M; Toledo L; Giné R; Vázquez C
    Rev Neurol; 1998 Jan; 26(149):77-9. PubMed ID: 9533212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic characterization of an extra structurally abnormal chromosome associated with severe mental retardation: inv dup (15) (q13).
    Gorla N; Slavutsky I; Lisanti J; Pedrazzini E; Vanella L; Larripa I
    Hereditas; 1998; 129(1):1-5. PubMed ID: 9868924
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 15q11-13 region and the autistic disorder.
    Sabry MA; Farag TI
    J Intellect Disabil Res; 1998 Jun; 42 ( Pt 3)():259. PubMed ID: 9678411
    [No Abstract]   [Full Text] [Related]  

  • 12. Maternal derivation of inv dup (22) and clinical variation in cat-eye syndrome.
    Tupler R; Hoeller A; Pezzolo A; Maraschio P
    Ann Genet; 1994; 37(3):153-5. PubMed ID: 7847799
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetic studies of autistic disorder and chromosome 7.
    Ashley-Koch A; Wolpert CM; Menold MM; Zaeem L; Basu S; Donnelly SL; Ravan SA; Powell CM; Qumsiyeh MB; Aylsworth AS; Vance JM; Gilbert JR; Wright HH; Abramson RK; DeLong GR; Cuccaro ML; Pericak-Vance MA
    Genomics; 1999 Nov; 61(3):227-36. PubMed ID: 10552924
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect.
    Mignon C; Malzac P; Moncla A; Depetris D; Roeckel N; Croquette MF; Mattei MG
    Eur J Hum Genet; 1996; 4(2):88-100. PubMed ID: 8744026
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
    Vincent JB; Horike SI; Choufani S; Paterson AD; Roberts W; Szatmari P; Weksberg R; Fernandez B; Scherer SW
    J Med Genet; 2006 May; 43(5):429-34. PubMed ID: 16556609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An association analysis of candidate genes on chromosome 15 q11-13 and autism spectrum disorder.
    Curran S; Powell J; Neale BM; Dworzynski K; Li T; Murphy D; Bolton PF
    Mol Psychiatry; 2006 Aug; 11(8):709-13. PubMed ID: 16868570
    [No Abstract]   [Full Text] [Related]  

  • 19. Ring chromosome 22 and autism: report and review.
    MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
    Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
    Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.