BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 25166435)

  • 1. Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland.
    Laczmańska I; Szczepaniak M; Jakubiak A; Stembalska A
    Adv Clin Exp Med; 2014; 23(4):517-21. PubMed ID: 25166435
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplification.
    De Luca A; Bottillo I; Dasdia MC; Morella A; Lanari V; Bernardini L; Divona L; Giustini S; Sinibaldi L; Novelli A; Torrente I; Schirinzi A; Dallapiccola B
    J Med Genet; 2007 Dec; 44(12):800-8. PubMed ID: 18055911
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evaluation of Molecular and Clinical Findings in Children With Neurofibromatosis Type 1: Identification of 15 Novel Variants.
    Bildirici Y; Kocaaga A; Karademir-Arslan CN; Yimenicioglu S
    Pediatr Neurol; 2023 Dec; 149():69-74. PubMed ID: 37806041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NF1 single and multi-exons copy number variations in neurofibromatosis type 1.
    Imbard A; Pasmant E; Sabbagh A; Luscan A; Soares M; Goussard P; Blanché H; Laurendeau I; Ferkal S; Vidaud M; Pinson S; Bellanne-Chantelot C; Vidaud D; Wolkenstein P; ; Parfait B
    J Hum Genet; 2015 Apr; 60(4):221-4. PubMed ID: 25631097
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAE.
    Ben-Salem S; Al-Shamsi AM; Ali BR; Al-Gazali L
    Childs Nerv Syst; 2014 Jul; 30(7):1183-9. PubMed ID: 24413922
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Thirty-nine novel neurofibromatosis 1 (NF1) gene mutations identified in Slovak patients.
    Nemethova M; Bolcekova A; Ilencikova D; Durovcikova D; Hlinkova K; Hlavata A; Kovacs L; Kadasi L; Zatkova A
    Ann Hum Genet; 2013 Sep; 77(5):364-79. PubMed ID: 23758643
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Neurofibromatosis type 1 or Von Recklinghausen's disease].
    Pinson S; Wolkenstein P
    Rev Med Interne; 2005 Mar; 26(3):196-215. PubMed ID: 15777582
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurofibromatosis type 1: Expanded variant spectrum with multiplex ligation-dependent probe amplification and genotype-phenotype correlation in 138 Turkish patients.
    Güneş N; Yeşil G; Geyik F; Kasap B; Celkan T; Kebudi R; Tüysüz B
    Ann Hum Genet; 2021 Sep; 85(5):155-165. PubMed ID: 33877690
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Neurofibromatosis type 1 (von Recklinghausen's disease or peripheral neurofibromatosis): from phenotype to gene].
    Sabol Z; Kipke-Sabol L
    Lijec Vjesn; 2005; 127(11-12):303-11. PubMed ID: 16583938
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.
    Gabriele AL; Ruggieri M; Patitucci A; Magariello A; Conforti FL; Mazzei R; Muglia M; Ungaro C; Di Palma G; Citrigno L; Sproviero W; Gambardella A; Quattrone A
    Childs Nerv Syst; 2011 Apr; 27(4):635-8. PubMed ID: 20927530
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients.
    Wimmer K; Yao S; Claes K; Kehrer-Sawatzki H; Tinschert S; De Raedt T; Legius E; Callens T; Beiglböck H; Maertens O; Messiaen L
    Genes Chromosomes Cancer; 2006 Mar; 45(3):265-76. PubMed ID: 16283621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.
    N Abdel-Aziz N; Y El-Kamah G; A Khairat R; R Mohamed H; Z Gad Y; El-Ghor AM; Amr KS
    Mol Genet Genomic Med; 2021 Dec; 9(12):e1631. PubMed ID: 34080803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?
    Yang CC; Happle R; Chao SC; Yu-Yun Lee J; Chen W
    J Am Acad Dermatol; 2008 Mar; 58(3):493-7. PubMed ID: 18280349
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.
    Mudau MM; Dillon B; Smal C; Feben C; Honey E; Carstens N; Krause A
    Front Genet; 2024; 15():1331278. PubMed ID: 38596211
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene.
    Colman SD; Williams CA; Wallace MR
    Nat Genet; 1995 Sep; 11(1):90-2. PubMed ID: 7550323
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of the whole NF1 gene in a three-generation family with neurofibromatosis type 1.
    Du Q; Chen H; Zhou H
    Neurol Sci; 2022 Feb; 43(2):1295-1301. PubMed ID: 34089417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NF1 mutation analysis using a combined heteroduplex/SSCP approach.
    Abernathy CR; Rasmussen SA; Stalker HJ; Zori R; Driscoll DJ; Williams CA; Kousseff BG; Wallace MR
    Hum Mutat; 1997; 9(6):548-54. PubMed ID: 9195229
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of large NF1 duplications reciprocal to NAHR-mediated type-1 NF1 deletions.
    Kehrer-Sawatzki H; Bengesser K; Callens T; Mikhail F; Fu C; Hillmer M; Walker ME; Saal HM; Lacassie Y; Cooper DN; Messiaen L
    Hum Mutat; 2014 Dec; 35(12):1469-75. PubMed ID: 25205021
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridization.
    Leppig KA; Viskochil D; Neil S; Rubenstein A; Johnson VP; Zhu XL; Brothman AR; Stephens K
    Cytogenet Cell Genet; 1996; 72(1):95-8. PubMed ID: 8565646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A case of growth hormone deficiency combined with neurofibromatosis Type 1 and its gene analysis].
    Long X; Xiong J; Mo Z; Zhang Q; Jin P
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2018 Jul; 43(7):811-815. PubMed ID: 30124220
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.