BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 15235024)

  • 1. Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.
    Tsilchorozidou T; Menko FH; Lalloo F; Kidd A; De Silva R; Thomas H; Smith P; Malcolmson A; Dore J; Madan K; Brown A; Yovos JG; Tsaligopoulos M; Vogiatzis N; Baser ME; Wallace AJ; Evans DG
    J Med Genet; 2004 Jul; 41(7):529-34. PubMed ID: 15235024
    [No Abstract]   [Full Text] [Related]  

  • 2. Neurofibromatosis type 2 in Phelan-McDermid syndrome: Institutional experience and review of the literature.
    Ziats CA; Jain L; McLarney B; Vandenboom E; DuPont BR; Rogers C; Sarasua S; Nevado J; Cordisco EL; Phelan K; Boccuto L
    Eur J Med Genet; 2020 Nov; 63(11):104042. PubMed ID: 32822873
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ring chromosome 22 and neurofibromatosis.
    Tommerup N; Warburg M; Gieselmann V; Hansen BR; Koch J; Petersen GB
    Clin Genet; 1992 Oct; 42(4):171-7. PubMed ID: 1424240
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Constitutional de novo interstitial deletion of 8 Mb on chromosome 22q12.1-12.3 encompassing the neurofibromatosis type 2 (NF2) locus in a dysmorphic girl with severe malformations.
    Barbi G; Rossier E; Vossbeck S; Hummler H; Lang D; Flock F; Terinde R; Wirth J; Vogel W; Kehrer-Sawatzki H
    J Med Genet; 2002 Feb; 39(2):E6. PubMed ID: 11836375
    [No Abstract]   [Full Text] [Related]  

  • 5. Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma.
    Zirn B; Arning L; Bartels I; Shoukier M; Hoffjan S; Neubauer B; Hahn A
    Clin Genet; 2012 Jan; 81(1):82-7. PubMed ID: 21175598
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical Reasoning: A common cause for Phelan-McDermid syndrome and neurofibromatosis type 2: One ring to bind them.
    Lyons-Warren AM; Cheung SW; Holder JL
    Neurology; 2017 Oct; 89(17):e205-e209. PubMed ID: 29061681
    [No Abstract]   [Full Text] [Related]  

  • 7. Neurofibromatosis type 2 in an adolescent boy with polyneuropathy and a mutation in the NF2 gene.
    Overweg-Plandsoen WC; Brouwer-Mladin R; Merel P; de Vries L; Bijlsma EK
    J Neurol; 1996 Oct; 243(10):724-6. PubMed ID: 8923306
    [No Abstract]   [Full Text] [Related]  

  • 8. Neurofibromatosis type 2: genetic and clinical features.
    Evans DG
    Ear Nose Throat J; 1999 Feb; 78(2):97-100. PubMed ID: 10089694
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?
    Bruder CE; Ichimura K; Blennow E; Ikeuchi T; Yamaguchi T; Yuasa Y; Collins VP; Dumanski JP
    Genes Chromosomes Cancer; 1999 Jun; 25(2):184-90. PubMed ID: 10338003
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cat eye syndrome associated with schizophrenia.
    Domula M; Schulze D; Felber W; Gallinat J; Lang UE
    Pharmacopsychiatry; 2007 Jan; 40(1):38-9. PubMed ID: 17327960
    [No Abstract]   [Full Text] [Related]  

  • 11. [Selected problems of neurofibromatosis with presentation of a case of multiple intracranial and intramedullary tumors].
    Stachura Z; Zralek C; Siemianowicz S; Kiczka-Zralek M; Zawadzki T; Kluczewska E; Giec-Lorenc A
    Neurol Neurochir Pol; 1998; 32(6):1563-9. PubMed ID: 10358844
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2.
    Arai E; Ikeuchi T; Karasawa S; Tamura A; Yamamoto K; Kida M; Ichimura K; Yuasa Y; Tonomura A
    Am J Med Genet; 1992 Sep; 44(2):163-7. PubMed ID: 1456285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46,X,t(X;22)(p11.2;q11.2).
    Bovie C; Holden ST; Schroer A; Smith E; Trump D; Raymond FL
    J Med Genet; 2003 Sep; 40(9):682-4. PubMed ID: 12960214
    [No Abstract]   [Full Text] [Related]  

  • 14. Adult-onset psychosis and clinical genetics: a case of Phelan-McDermid syndrome.
    Messias E; Kaley SN; McKelvey KD
    J Neuropsychiatry Clin Neurosci; 2013; 25(4):E27. PubMed ID: 24247879
    [No Abstract]   [Full Text] [Related]  

  • 15. [Neurofibromatosis ].
    Wakabayashi T; Saito K; Yoshida J
    Nihon Rinsho; 2005 Sep; 63 Suppl 9():164-9. PubMed ID: 16201518
    [No Abstract]   [Full Text] [Related]  

  • 16. Neurofibromatosis type 2 in an infant presenting with visual impairment confirmed by genetic mutation analysis.
    Kim JE; Ruttum MS
    Retina; 2005; 25(7):938-40. PubMed ID: 16205576
    [No Abstract]   [Full Text] [Related]  

  • 17. Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.
    Fiegler H; Gribble SM; Burford DC; Carr P; Prigmore E; Porter KM; Clegg S; Crolla JA; Dennis NR; Jacobs P; Carter NP
    J Med Genet; 2003 Sep; 40(9):664-70. PubMed ID: 12960211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.
    Buckley PG; Mantripragada KK; Díaz de Ståhl T; Piotrowski A; Hansson CM; Kiss H; Vetrie D; Ernberg IT; Nordenskjöld M; Bolund L; Sainio M; Rouleau GA; Niimura M; Wallace AJ; Evans DG; Grigelionis G; Menzel U; Dumanski JP
    Hum Mutat; 2005 Dec; 26(6):540-9. PubMed ID: 16287142
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial disease in 22q13 duplication syndrome.
    Frye RE
    J Child Neurol; 2012 Jul; 27(7):942-9. PubMed ID: 22378673
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurofibromatosis 2.
    Kitamura K; Takahashi K; Kakoi H
    Adv Otorhinolaryngol; 2000; 56():244-8. PubMed ID: 10868241
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.