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Variegated translocation mosaicism in human skin fibroblast cultures.
Hoehn H, Bryant EM, Au K, Norwood TH, Boman H, Martin GM. Hoehn H, et al. Among authors: au k. Cytogenet Cell Genet. 1975;15(5):282-98. doi: 10.1159/000130526. Cytogenet Cell Genet. 1975. PMID: 1222585
Differences in human X isochromosomes.
Priest JH, Blackston RD, Au KS, Ray SL. Priest JH, et al. Among authors: au ks. J Med Genet. 1975 Dec;12(4):378-89. doi: 10.1136/jmg.12.4.378. J Med Genet. 1975. PMID: 1219118 Free PMC article.
Effects of radical-scavenging enzymes and reduced oxygen exposure on growth and chromosome abnormalities of Werner syndrome cultured skin fibroblasts.
Salk D, Au K, Hoehn H, Martin GM. Salk D, et al. Among authors: au k. Hum Genet. 1981;57(3):269-75. doi: 10.1007/BF00278942. Hum Genet. 1981. PMID: 7250969
Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts.
Salk D, Bryant E, Au K, Hoehn H, Martin GM. Salk D, et al. Among authors: au k. Hum Genet. 1981;58(3):310-6. doi: 10.1007/BF00294930. Hum Genet. 1981. PMID: 7327553
Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.
Salk D, Au K, Hoehn H, Martin GM. Salk D, et al. Among authors: au k. Cytogenet Cell Genet. 1981;30(2):92-107. doi: 10.1159/000131596. Cytogenet Cell Genet. 1981. PMID: 7273860
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. Salk D, et al. Among authors: au k. Cytogenet Cell Genet. 1981;30(2):108-17. doi: 10.1159/000131597. Cytogenet Cell Genet. 1981. PMID: 7273855
Somatic stability of variant C-band heterochromatin.
Hoehn H, Au K, Karp LE, Martin GM. Hoehn H, et al. Among authors: au k. Hum Genet. 1977 Feb 11;35(2):163-8. doi: 10.1007/BF00393965. Hum Genet. 1977. PMID: 844861
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locus.
Kirkpatrick TJ, Au KS, Mastrobattista JM, McCready ME, Bulman DE, Northrup H. Kirkpatrick TJ, et al. Among authors: au ks. J Med Genet. 2003 Jan;40(1):42-4. doi: 10.1136/jmg.40.1.42. J Med Genet. 2003. PMID: 12525541 Free PMC article. No abstract available.
Cytogenetic aspects of Werner syndrome.
Salk D, Au K, Hoehn H, Martin GM. Salk D, et al. Among authors: au k. Adv Exp Med Biol. 1985;190:541-6. doi: 10.1007/978-1-4684-7853-2_27. Adv Exp Med Biol. 1985. PMID: 4083162 No abstract available.
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele.
Au KS, Northrup H, Kirkpatrick TJ, Volcik KA, Fletcher JM, Townsend IT, Blanton SH, Tyerman GH, Villarreal G, King TM. Au KS, et al. Am J Med Genet A. 2005 Dec 15;139(3):194-8. doi: 10.1002/ajmg.a.31002. Am J Med Genet A. 2005. PMID: 16283668 Free PMC article.
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