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 *

143 related articles for article (PubMed ID: 8565626)

  • 1. Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosis.
    LeGuern E; Ravise N; Gouider R; Gugenheim M; Lopes J; Bouche P; Agid Y; Brice A
    Cytogenet Cell Genet; 1996; 72(1):20-5. PubMed ID: 8565626
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion.
    Kim SM; Chung KW; Choi BO; Yoon ES; Choi JY; Park KD; Sunwoo IN
    Exp Mol Med; 2004 Feb; 36(1):28-35. PubMed ID: 15031668
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.
    Lorenzetti D; Pareyson D; Sghirlanzoni A; Roa BB; Abbas NE; Pandolfo M; Di Donato S; Lupski JR
    Am J Hum Genet; 1995 Jan; 56(1):91-8. PubMed ID: 7825607
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats.
    Gagic M; Markovic MK; Kecmanovic M; Keckarevic D; Mladenovic J; Dackovic J; Milic-Rasic V; Romac S
    Clin Chem Lab Med; 2016 May; 54(5):773-80. PubMed ID: 26479344
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs.
    Seeman P; Mazanec R; Zidar J; Hrusáková S; Ctvrtecková M; Rautenstrauss B
    Int J Mol Med; 2000 Oct; 6(4):421-6. PubMed ID: 10998431
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP).
    Le Guern E; Sturtz F; Gugenheim M; Gouider R; Bonnebouche C; Ravisé N; Gonnaud PM; Tardieu S; Bouche P; Chazot G
    Cytogenet Cell Genet; 1994; 65(4):261-4. PubMed ID: 7903071
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure].
    Pou Serradell A; Espadaler JM; Aragonés JM; Bufill E; Alameda F; Vílchez JJ; Sevilla T; Piqueras A; Palau F; Bort S
    Neurologia; 1995 Nov; 10(9):367-74. PubMed ID: 8554792
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
    Chance PF
    Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.
    Lopes J; LeGuern E; Gouider R; Tardieu S; Abbas N; Birouk N; Gugenheim M; Bouche P; Agid Y; Brice A
    Am J Hum Genet; 1996 Jun; 58(6):1223-30. PubMed ID: 8651299
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation.
    Leonardis L; Zidar J; Ekici A; Peterlin B; Rautenstrauss B
    Int J Mol Med; 1998 Feb; 1(2):495-501. PubMed ID: 9852256
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
    LeGuern E; Gouider R; Ravisé N; Lopes J; Tardieu S; Gugenheim M; Abbas N; Bouche P; Agid Y; Brice A
    Hum Mol Genet; 1996 Jan; 5(1):103-6. PubMed ID: 8789446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
    Pou Serradell A; Monells J; Téllez MJ; Fossas P; Löfgren A; Meuleman J; Timmerman V; De Jonghe P; Ceuterick C; Martin JJ
    Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1.
    Mariman EC; Gabreëls-Festen AA; van Beersum SE; Jongen PJ; Ropers HH; Gabreëls FJ
    Hum Genet; 1993 Aug; 92(1):87-90. PubMed ID: 8396068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.
    Inoue K; Dewar K; Katsanis N; Reiter LT; Lander ES; Devon KL; Wyman DW; Lupski JR; Birren B
    Genome Res; 2001 Jun; 11(6):1018-33. PubMed ID: 11381029
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies.
    Stronach EA; Clark C; Bell C; Löfgren A; McKay NG; Timmerman V; Van Broeckhoven C; Haites NE
    J Peripher Nerv Syst; 1999; 4(2):117-22. PubMed ID: 10442687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.
    Verhalle D; Löfgren A; Nelis E; Dehaene I; Theys P; Lammens M; Dom R; Van Broeckhoven C; Robberecht W
    Ann Neurol; 1994 Jun; 35(6):704-8. PubMed ID: 8210227
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.
    Potocki L; Chen KS; Park SS; Osterholm DE; Withers MA; Kimonis V; Summers AM; Meschino WS; Anyane-Yeboa K; Kashork CD; Shaffer LG; Lupski JR
    Nat Genet; 2000 Jan; 24(1):84-7. PubMed ID: 10615134
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17.
    Chance PF; Abbas N; Lensch MW; Pentao L; Roa BB; Patel PI; Lupski JR
    Hum Mol Genet; 1994 Feb; 3(2):223-8. PubMed ID: 8004087
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overview of hereditary neuropathy with liability to pressure palsies.
    Chance PF
    Ann N Y Acad Sci; 1999 Sep; 883():14-21. PubMed ID: 10586225
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
    Chance PF; Alderson MK; Leppig KA; Lensch MW; Matsunami N; Smith B; Swanson PD; Odelberg SJ; Disteche CM; Bird TD
    Cell; 1993 Jan; 72(1):143-51. PubMed ID: 8422677
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.