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 *

91 related articles for article (PubMed ID: 15235033)

  • 1. FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour.
    Finelli P; Natacci F; Bonati MT; Gottardi G; Engelen JJ; de Die-Smulders CE; Sala M; Giardino D; Larizza L
    J Med Genet; 2004 Jul; 41(7):e90. PubMed ID: 15235033
    [No Abstract]   [Full Text] [Related]  

  • 2. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
    Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
    Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
    Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
    Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Should the chromosome region 15q11q13 be tested systematically by FISH in the case of an autistic-like syndrome?
    Yardin C; Esclaire F; Laroche C; Terro F; Barthe D; Bonnefont JP; Gilbert B
    Clin Genet; 2002 Apr; 61(4):310-3. PubMed ID: 12030899
    [No Abstract]   [Full Text] [Related]  

  • 5. Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.
    Vorsanova SG; Yurov IY; Demidova IA; Voinova-Ulas VY; Kravets VS; Solov'ev IV; Gorbachevskaya NL; Yurov YB
    Neurosci Behav Physiol; 2007 Jul; 37(6):553-8. PubMed ID: 17657425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders].
    Vorsanova SG; Iurov IIu; Demidova IA; Voinova-Ulas VIu; Kravets VS; Solov'ev IV; Gorbachevskaia NL; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2006; 106(6):52-7. PubMed ID: 16841485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A de novo direct duplication of 16q22.1 --> q23.1 in a boy with midface hypoplasia and mental retardation.
    Tokutomi T; Wada T; Nakagawa E; Saitoh S; Sasaki M
    Am J Med Genet A; 2009 Nov; 149A(11):2560-3. PubMed ID: 19842195
    [No Abstract]   [Full Text] [Related]  

  • 8. Autistic disorder and 22q11.2 duplication.
    Mukaddes NM; Herguner S
    World J Biol Psychiatry; 2007; 8(2):127-30. PubMed ID: 17455106
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo partial duplication of chromosome 7p in a male with autistic disorder.
    Wolpert CM; Donnelly SL; Cuccaro ML; Hedges DJ; Poole CP; Wright HH; Gilbert JR; Pericak-Vance MA
    Am J Med Genet; 2001 Apr; 105(3):222-5. PubMed ID: 11353439
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome "hot spot" linked to autism.
    Harv Ment Health Lett; 2008 May; 24(11):7. PubMed ID: 18677793
    [No Abstract]   [Full Text] [Related]  

  • 11. Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12).
    Moog U; Engelen JJ; Weber BW; Van Gelderen M; Steyaert J; Baas F; Sijstermans HM; Fryns JP
    Genet Couns; 2004; 15(1):73-80. PubMed ID: 15083703
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A case of inverted tandem partial duplication of 12p].
    Moreno García M; Sánchez del Pozo J; Barreiro Miranda E
    An Esp Pediatr; 1999 Feb; 50(2):181-4. PubMed ID: 10199032
    [No Abstract]   [Full Text] [Related]  

  • 13. Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.
    Simic M; Turk J
    Eur Child Adolesc Psychiatry; 2004 Dec; 13(6):389-93. PubMed ID: 15619052
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of chromosome aberrations in Chinese children with autism using G-banding and BAC FISH.
    Liu QJ; Ma F; Li D; Wang XW; Tian WY; Chen Y; Feng JB; Lu X; Chen DQ; Chen XN; Shen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):254-7. PubMed ID: 15952108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A hot spot of genetic instability in autism.
    Eichler EE; Zimmerman AW
    N Engl J Med; 2008 Feb; 358(7):737-9. PubMed ID: 18184953
    [No Abstract]   [Full Text] [Related]  

  • 17. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
    Ullmann R; Turner G; Kirchhoff M; Chen W; Tonge B; Rosenberg C; Field M; Vianna-Morgante AM; Christie L; Krepischi-Santos AC; Banna L; Brereton AV; Hill A; Bisgaard AM; Müller I; Hultschig C; Erdogan F; Wieczorek G; Ropers HH
    Hum Mutat; 2007 Jul; 28(7):674-82. PubMed ID: 17480035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders].
    Vorsanova SG; Voinova VIu; Iurov IIu; Kurinnaia OS; Demidova IA; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2009; 109(6):54-64. PubMed ID: 19672229
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1.
    Utine GE; Melotte C; Vermeesch JR; Fryns JP
    Genet Couns; 2005; 16(4):407-12. PubMed ID: 16440884
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders.
    Vorsanova SG; Voinova VY; Yurov IY; Kurinnaya OS; Demidova IA; Yurov YB
    Neurosci Behav Physiol; 2010 Sep; 40(7):745-56. PubMed ID: 20635215
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.