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Results: 1-8 |
Results: 8

Authors: BIRCHMACHIN MA TINDALL M TURNER R HALDANE F REES JL
Citation: Ma. Birchmachin et al., MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTO RATHER THAN CHRONOLOGICAL AGING, Journal of investigative dermatology, 110(2), 1998, pp. 149-152

Authors: BIRCHMACHIN MA HALDANE F REES JL
Citation: Ma. Birchmachin et al., MITOCHONDRIAL-DNA DELETIONS IN HUMAN SKIN REFLECT PHOTOAGEING RATHER THAN CHRONOLOGICAL AGING, Journal of investigative dermatology, 109(3), 1997, pp. 436-436

Authors: BIRCHMACHIN MA HEALY E TURNER R HALDANE F BELGAID CE DARLINGTON S STEPHENSON AM MUNRO C MESSENGER AG REES JL
Citation: Ma. Birchmachin et al., MAPPING OF MONILETHRIX TO THE TYPE-II KERATIN GENE-CLUSTER AT CHROMOSOME 12Q13 IN 3 NEW FAMILIES, INCLUDING ONE WITH VARIABLE EXPRESSIVITY, British journal of dermatology, 137(3), 1997, pp. 339-343

Authors: VALVERDE P HEALY E SIKKINK S HALDANE F THODY AJ CAROTHERS A JACKSON IJ REES JL
Citation: P. Valverde et al., THE ASP84GLU VARIANT OF THE MELANOCORTIN-1 RECEPTOR (MC1R) IS ASSOCIATED WITH MELANOMA, Human molecular genetics, 5(10), 1996, pp. 1663-1666

Authors: ARMSTRONG M HALDANE F AVERY PJ MITCHESON J STEWART MW TURNBULL DM WALKER M
Citation: M. Armstrong et al., RELATIONSHIP BETWEEN INSULIN SENSITIVITY AND INSULIN-RECEPTOR SUBSTRATE-1 MUTATIONS IN NONDIABETIC RELATIVES OF NIDDM FAMILIES, Diabetic medicine, 13(4), 1996, pp. 341-345

Authors: ARMSTRONG M HALDANE F TAYLOR RW ALBERTI KGMM TURNBULL DM WALKER M
Citation: M. Armstrong et al., HUMAN INSULIN-RECEPTOR SUBSTRATE-1 - VARIANT SEQUENCES IN FAMILIAL NONINSULIN-DEPENDENT DIABETES-MELLITUS, Diabetic medicine, 13(2), 1996, pp. 133-138

Authors: TAYLOR RW CHINNERY PF HALDANE F MORRIS AAM BINDOFF LA WILSON J TURNBULL DM
Citation: Rw. Taylor et al., MELAS ASSOCIATED WITH A MUTATION IN THE VALINE TRANSFER-RNA GENE OF MITOCHONDRIAL-DNA, Annals of neurology, 40(3), 1996, pp. 459-462

Authors: MORTEN KJ HALDANE F WEBER K POULTON J BINDOFF L
Citation: Kj. Morten et al., A MTDNA MUTATION ASSOCIATED WITH AN RNA PROCESSING DEFECT AND BIOCHEMICAL-ABNORMALITIES IN SKELETAL-MUSCLE (LIMITATIONS OF RHO ZERO LINES), American journal of human genetics, 53(3), 1993, pp. 1743-1743
Risultati: 1-8 |