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4. Spectral karyotyping of Werner syndrome fibroblast cultures. Melcher R; von Golitschek R; Steinlein C; Schindler D; Neitzel H; Kainer K; Schmid M; Hoehn H Cytogenet Cell Genet; 2000; 91(1-4):180-5. PubMed ID: 11173853 [TBL] [Abstract][Full Text] [Related]
5. Chromosomal diagnosis of the Werner syndrome. Jaramillo C; Jorgenson RJ; Miles DA; Moore CM Birth Defects Orig Artic Ser; 1985; 21(2):119-26. PubMed ID: 4041574 [No Abstract] [Full Text] [Related]
6. A population and cytogenetic study of the Werner syndrome in Sardinia. Fraccaro M; Scappaticci S; Cerimele D Adv Exp Med Biol; 1985; 190():547-52. PubMed ID: 4083163 [No Abstract] [Full Text] [Related]
7. Variegated translocation mosaicism in human skin fibroblast cultures. Hoehn H; Bryant EM; Au K; Norwood TH; Boman H; Martin GM Cytogenet Cell Genet; 1975; 15(5):282-98. PubMed ID: 1222585 [TBL] [Abstract][Full Text] [Related]
8. In vitro studies of Werner syndrome cells: aberrant growth and chromosome behavior. Salk D Basic Life Sci; 1985; 35():419-26. PubMed ID: 4062821 [No Abstract] [Full Text] [Related]
10. Spontaneous and X-ray-induced chromosomal aberrations in Werner syndrome cells detected by FISH using chromosome-specific painting probes. Grigorova M; Balajee AS; Natarajan AT Mutagenesis; 2000 Jul; 15(4):303-10. PubMed ID: 10887208 [TBL] [Abstract][Full Text] [Related]
11. Chromosome breaks in Werner's syndrome and their prevention in vitro by radical-scavenging enzymes. Nordenson I Hereditas; 1977; 87(2):151-4. PubMed ID: 608842 [No Abstract] [Full Text] [Related]
12. A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome. Brown WT; Kieras FJ; Houck GE; Dutkowski R; Jenkins EC Adv Exp Med Biol; 1985; 190():229-44. PubMed ID: 3909767 [No Abstract] [Full Text] [Related]
13. Atypical meningioma in Werner syndrome: a case report. Marton E; Bonaldi L; Busato S; Longatti P J Neurooncol; 2006 Sep; 79(2):181-5. PubMed ID: 16598422 [TBL] [Abstract][Full Text] [Related]
14. Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndrome. Scappaticci S; Forabosco A; Borroni G; Orecchia G; Fraccaro M Ann Genet; 1990; 33(1):5-8. PubMed ID: 2369072 [TBL] [Abstract][Full Text] [Related]
15. Extension of the life span in patients with Werner syndrome. Yokote K; Saito Y J Am Geriatr Soc; 2008 Sep; 56(9):1770-1. PubMed ID: 19166457 [No Abstract] [Full Text] [Related]
16. Telomere dysfunction as a cause of genomic instability in Werner syndrome. Crabbe L; Jauch A; Naeger CM; Holtgreve-Grez H; Karlseder J Proc Natl Acad Sci U S A; 2007 Feb; 104(7):2205-10. PubMed ID: 17284601 [TBL] [Abstract][Full Text] [Related]
17. Neurological involvement in Werner's syndrome: clinical and biopsy study of a familial case. Malandrini A; Dotti MT; Villanova M; Battisti C; Federico A Eur Neurol; 2000; 44(3):187-9. PubMed ID: 11053972 [No Abstract] [Full Text] [Related]
18. Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner's syndrome skin fibroblasts. Salk D; Au K; Hoehn H; Stenchever MR; Martin GM Cytogenet Cell Genet; 1981; 30(2):108-17. PubMed ID: 7273855 [TBL] [Abstract][Full Text] [Related]
19. Comparative aspects of the Werner syndrome gene. Oshima J In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074 [TBL] [Abstract][Full Text] [Related]