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 *

120 related articles for article (PubMed ID: 1670508)

  • 21. [Cardio-cutaneous syndromes of genetic origin].
    Pernot C; Worms AM; Henry M
    Nouv Presse Med; 1973 Oct; 2(36):2395-400. PubMed ID: 4201000
    [No Abstract]   [Full Text] [Related]  

  • 22. The morbid cutaneous anatomy of the human genome.
    Epstein EH
    Arch Dermatol; 1993 Nov; 129(11):1417-23. PubMed ID: 8239700
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Symposium on Linkage of von Recklinghausen Neurofibromatosis (NF1). Closing in on the gene for von Recklinghausen neurofibromatosis.
    Genomics; 1987 Dec; 1(4):335-83. PubMed ID: 3130303
    [No Abstract]   [Full Text] [Related]  

  • 24. Characterization of naturally occurring cutaneous neurofibromatosis in Holstein cattle. A disorder resembling neurofibromatosis type 1 in humans.
    Sartin EA; Doran SE; Riddell MG; Herrera GA; Tennyson GS; D'Andrea G; Whitley RD; Collins FS
    Am J Pathol; 1994 Nov; 145(5):1168-74. PubMed ID: 7977647
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Surgical management of neurofibromatosis.
    Parsons CM; Canter RJ; Khatri VP
    Surg Oncol Clin N Am; 2009 Jan; 18(1):175-96, x. PubMed ID: 19056048
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Hereditary neurofibromatosis with a wide phenotypic spectrum (the family Sn.)].
    PHILIPPART M
    J Genet Hum; 1961 Dec; 10():338-46. PubMed ID: 14486194
    [No Abstract]   [Full Text] [Related]  

  • 27. Inheritance and the pigmentary dispersion syndrome.
    Mandelkorn RM; Hoffman ME; Olander KW; Zimmerman TJ; Harsha D
    Ophthalmic Paediatr Genet; 1985 Aug; 6(1-2):325-31. PubMed ID: 4069593
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Multiple segmental neurofibromatosis.
    Lee SH; Roh MR; Kim SC
    J Dermatol; 2012 Sep; 39(9):810-1. PubMed ID: 22393916
    [No Abstract]   [Full Text] [Related]  

  • 29. [Lisch nodules: description of 2 clinical cases and their significance].
    Menard L; Magnaval G; Donnio A; Ayeboua L; Richer R; Merle H
    J Fr Ophtalmol; 2001 Nov; 24(9):966-70. PubMed ID: 11912842
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Gene location in neurofibromatosis.
    Stambolian D; Zackai EH
    Am J Med Genet; 1988 Apr; 29(4):963-5. PubMed ID: 3135756
    [No Abstract]   [Full Text] [Related]  

  • 31. [Genetics of neurofibromatosis: recent progress and prospects].
    Maillet-Vioud M; Narod S; Assouline D; Sobol H; Fischer G; Robert JM; Lenoir GM
    Rev Neurol (Paris); 1991; 147(10):644-52. PubMed ID: 1763253
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital Horner's syndrome does not alter Lisch nodule formation.
    Mindel JS; Rubenstein AE; Wallace S; Aron AM; Halperin J
    Ann Neurol; 1994 Jan; 35(1):123-4. PubMed ID: 8285584
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Polymorphism of neurofibromatosis: 2 familial cases; a case of crossed gigantism].
    PHILIPPART M
    Arch Belg Dermatol Syphiligr; 1961 Dec; 17():314-8. PubMed ID: 14486195
    [No Abstract]   [Full Text] [Related]  

  • 34. Lisch nodules associated with neurofibromatosis type 1.
    Yeung H
    J Pediatr Ophthalmol Strabismus; 2007; 44(3):151, 177. PubMed ID: 17542434
    [No Abstract]   [Full Text] [Related]  

  • 35. More on the frequency of segmental neurofibromatosis.
    Wolkenstein P; Mahmoudi A; Zeller J; Revuz J
    Arch Dermatol; 1995 Dec; 131(12):1465. PubMed ID: 7492147
    [No Abstract]   [Full Text] [Related]  

  • 36. Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene.
    Upadhyaya M; Shaw DJ; Harper PS
    Hum Mutat; 1994; 4(2):83-101. PubMed ID: 7981724
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Late-onset neurofibromatosis revealing NF1 mutation.
    Uchiyama M; Sakai N; Maeda T; Tsuboi R; Mitsuhashi Y
    J Dermatol; 2015 Jan; 42(1):104-5. PubMed ID: 25470215
    [No Abstract]   [Full Text] [Related]  

  • 38. [Dyscromic neurocutaneous syndromes].
    Sola-Casas MA; Salleras-Redonnet M
    Rev Neurol; 1997 Sep; 25 Suppl 3():S259-64. PubMed ID: 9273171
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular biology of the neurofibromatoses.
    Riccardi VM
    Semin Dermatol; 1993 Sep; 12(3):266-73. PubMed ID: 8217563
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Exclusion of allelism and close linkage between neurofibromatosis and multiple cartilaginous exostoses.
    Pai GS; Shapiro SD; Macpherson RI
    Am J Med Genet; 1989 Jan; 32(1):145. PubMed ID: 2495720
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.