141 related articles for article (PubMed ID: 2105472)
1. Paternal origin of new mutations in von Recklinghausen neurofibromatosis.
Jadayel D; Fain P; Upadhyaya M; Ponder MA; Huson SM; Carey J; Fryer A; Mathew CG; Barker DF; Ponder BA
Nature; 1990 Feb; 343(6258):558-9. PubMed ID: 2105472
[TBL] [Abstract][Full Text] [Related]
2. Mutations in von Recklinghausen neurofibromatosis: an hypothesis.
Zlotogora J
Am J Med Genet; 1993 Apr; 46(2):182-4. PubMed ID: 8484407
[TBL] [Abstract][Full Text] [Related]
3. The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations.
Riccardi VM; Dobson CE; Chakraborty R; Bontke C
Am J Med Genet; 1984 May; 18(1):169-76. PubMed ID: 6430086
[TBL] [Abstract][Full Text] [Related]
4. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
5. Parental origin of mutations in sporadic cases of Treacher Collins syndrome.
Splendore A; Jabs EW; Félix TM; Passos-Bueno MR
Eur J Hum Genet; 2003 Sep; 11(9):718-22. PubMed ID: 12939661
[TBL] [Abstract][Full Text] [Related]
6. Neurofibromatosis in Gothenburg, Sweden. IV. Genetic analyses.
Samuelsson B; Akesson HO
Neurofibromatosis; 1989; 2(2):107-15. PubMed ID: 2516454
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of von Recklinghausen neurofibromatosis in Dunedin, New Zealand.
Fuller LC; Cox B; Gardner RJ
Neurofibromatosis; 1989; 2(5-6):278-83. PubMed ID: 2518509
[TBL] [Abstract][Full Text] [Related]
8. A boy with neurofibromatosis 1 and Poland anomaly.
Alembik Y; Stoll C
Genet Couns; 1994; 5(2):167-70. PubMed ID: 7917126
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1.
Altarescu G; Brooks B; Kaplan Y; Eldar-Geva T; Margalioth EJ; Levy-Lahad E; Renbaum P
Hum Reprod; 2006 Aug; 21(8):2047-51. PubMed ID: 16740526
[TBL] [Abstract][Full Text] [Related]
11. Neurofibromatosis: novel and recurrent mutations in Turkish patients.
Terzi YK; Oguzkan S; Anlar B; Aysun S; Ayter S
Pediatr Neurol; 2007 Dec; 37(6):421-5. PubMed ID: 18021924
[TBL] [Abstract][Full Text] [Related]
12. Discounting an adverse maternal effect on severity of neurofibromatosis.
Riccardi VM; Wald JS
Pediatrics; 1987 Mar; 79(3):386-93. PubMed ID: 3103092
[TBL] [Abstract][Full Text] [Related]
13. Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic tool.
Elyakim S; Lerer I; Zlotogora J; Sagi M; Gelman-Kohan Z; Merin S; Abeliovich D
Am J Med Genet; 1994 Dec; 53(4):325-34. PubMed ID: 7864041
[TBL] [Abstract][Full Text] [Related]
14. Paternal age and sporadic neurofibromatosis 1: a case-control study and consideration of the methodologic issues.
Bunin GR; Needle M; Riccardi VM
Genet Epidemiol; 1997; 14(5):507-16. PubMed ID: 9358268
[TBL] [Abstract][Full Text] [Related]
15. Genetic and clinical considerations in six cases with neurofibromatosis type 1.
Buteică E; Stoicescu I; Burada F; Stănoiu B
Rom J Morphol Embryol; 2007; 48(3):243-8. PubMed ID: 17914490
[TBL] [Abstract][Full Text] [Related]
16. Parental origin of mutations of the retinoblastoma gene.
Dryja TP; Mukai S; Petersen R; Rapaport JM; Walton D; Yandell DW
Nature; 1989 Jun; 339(6225):556-8. PubMed ID: 2733786
[TBL] [Abstract][Full Text] [Related]
17. De novo mutations in familial adenomatous polyposis (FAP).
Ripa R; Bisgaard ML; Bülow S; Nielsen FC
Eur J Hum Genet; 2002 Oct; 10(10):631-7. PubMed ID: 12357334
[TBL] [Abstract][Full Text] [Related]
18. Example of somatic mosaicism in a series of de novo neurofibromatosis type 1 cases due to a maternally derived deletion.
Ainsworth PJ; Chakraborty PK; Weksberg R
Hum Mutat; 1997; 9(5):452-7. PubMed ID: 9143926
[TBL] [Abstract][Full Text] [Related]
19. Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?
Kehrer-Sawatzki H; Cooper DN
J Med Genet; 2008 Oct; 45(10):622-31. PubMed ID: 18511569
[TBL] [Abstract][Full Text] [Related]
20. Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.
Aretz S; Uhlhaas S; Caspari R; Mangold E; Pagenstecher C; Propping P; Friedl W
Eur J Hum Genet; 2004 Jan; 12(1):52-8. PubMed ID: 14523376
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]