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.
364 related articles for article (PubMed ID: 2511318)
21. A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage. Rodenhiser DI; Coulter-Mackie MB; Jung JH; Singh SM J Med Genet; 1991 Nov; 28(11):746-51. PubMed ID: 1685193 [TBL] [Abstract][Full Text] [Related]
22. [Von Recklinghausen neurofibromatosis in Lome, Togo]. Tchangaï-Walla K; Pitche P; Mijiyawa M; Grunitzky K Med Trop (Mars); 1995; 55(2):185-6. PubMed ID: 7565007 [No Abstract] [Full Text] [Related]
23. Noonan phenotype associated with neurofibromatosis. Allanson JE; Hall JG; Van Allen MI Am J Med Genet; 1985 Jul; 21(3):457-62. PubMed ID: 2411134 [TBL] [Abstract][Full Text] [Related]
24. [Analysis of the relation of the frequency of new gene mutations for Mendelian diseases to parental age]. Bazhenova MD; Kozlova SI; Al'tshuler BA; Tatishvili GG Genetika; 1984 Oct; 20(10):1726-32. PubMed ID: 6149974 [TBL] [Abstract][Full Text] [Related]
25. Results of the 1985 membership survey of the 'Vereniging Ziekte Van von Recklinghausen Nederland'. Steinebach M Neurofibromatosis; 1988; 1(3):166-71. PubMed ID: 3152464 [TBL] [Abstract][Full Text] [Related]
26. A genotype-phenotype correlation for quantitative autistic trait burden in neurofibromatosis 1. Morris SM; Gutmann DH Neurology; 2018 Feb; 90(8):377-379. PubMed ID: 29367450 [No Abstract] [Full Text] [Related]
27. Von Hippel-Lindau disease: a genetic study. Maher ER; Iselius L; Yates JR; Littler M; Benjamin C; Harris R; Sampson J; Williams A; Ferguson-Smith MA; Morton N J Med Genet; 1991 Jul; 28(7):443-7. PubMed ID: 1895313 [TBL] [Abstract][Full Text] [Related]
28. Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1. Corsello G; Antona V; Serra G; Zara F; Giambrone C; Lagalla L; Piccione M; Piro E Ital J Pediatr; 2018 Apr; 44(1):45. PubMed ID: 29618358 [TBL] [Abstract][Full Text] [Related]
29. Penetrance and variability in neurofibromatosis: a genetic study of 60 families. Carey JC; Laub JM; Hall BD Birth Defects Orig Artic Ser; 1979; 15(5B):271-81. PubMed ID: 118780 [No Abstract] [Full Text] [Related]
30. Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China. Liu X; Xu L; Zhang S; Xu Y Am J Med Genet; 1994 Nov; 53(2):192-5. PubMed ID: 7856647 [TBL] [Abstract][Full Text] [Related]
31. Neurofibromatosis. A clinical and genetic study of 96 cases in Gothenburg, Sweden. Samuelsson B; Axelsson R Acta Derm Venereol Suppl (Stockh); 1981; 95():67-71. PubMed ID: 6807042 [TBL] [Abstract][Full Text] [Related]
32. Large number of cutaneous neurofibromas beyond age-appropriate incidence in a patient with a large deletion of NF1. Yoshida Y; Ehara Y; Kosaki K; Yamamoto O J Dermatol; 2018 Mar; 45(3):363-364. PubMed ID: 29498099 [No Abstract] [Full Text] [Related]
33. [Effect of the sex of the progenitor on the clinical manifestations of neurofibromatosis]. Carnevale A; Santillán Y Rev Invest Clin; 1991; 43(4):359-63. PubMed ID: 1798871 [TBL] [Abstract][Full Text] [Related]
35. [Epidemiology and genetics of neurocutaneous syndrome, with special reference to Recklinghausen neurofibromatosis and tuberous sclerosis]. Ohno K No To Shinkei; 1984 Jan; 36(1):17-25. PubMed ID: 6428437 [No Abstract] [Full Text] [Related]
36. Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis. Mathew CG; Thorpe K; Easton DF; Carter C; Wallis C; Wong Z; Jeffreys AJ; Ponder BA J Med Genet; 1987 Sep; 24(9):524-6. PubMed ID: 3118029 [TBL] [Abstract][Full Text] [Related]
37. [Oral, facial and cranial manifestations of von Recklinghausen neurofibromatosis (NF)]. Keutel C; Vees B; Krimmel M; Cornelius CP; Schwenzer N Mund Kiefer Gesichtschir; 1997 Sep; 1(5):268-71. PubMed ID: 9410636 [TBL] [Abstract][Full Text] [Related]
38. Linkage analysis of Von Recklinghausen neurofibromatosis: chromosomes 4 and 19. Dietz JN; Robbins T; Cannon LA; Schwartz CE; Carey JC; Johnson JP; Kivlin J; Skolnick MH Genet Epidemiol; 1986; 3(5):313-21. PubMed ID: 3096816 [TBL] [Abstract][Full Text] [Related]
39. Dermatoglyphics in von Recklinghausen neurofibromatosis. Pallotta R; Carlone G; Petrucci A; Chiarelli F Am J Med Genet; 1989 Oct; 34(2):233-6. PubMed ID: 2510518 [TBL] [Abstract][Full Text] [Related]
40. [Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome]. Seemanová E; Zenker M Cas Lek Cesk; 2014; 153(5):242-5. PubMed ID: 25370770 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]