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Publisher: Wiley-Blackwell

Volume 62, Number 3, May 1998

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Free Content Phenylketonuria – a problem in eugenics
pp. 193-202(10)
Author: PENROSE, L. S.

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Free Content A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients
pp. 203-213(11)
Authors: YOUNG, J. M.; BURLEY, M. W.; JEREMIAH, S. J.; JEGANATHAN, D.; EKONG, R.; OSBORNE, J. P.; POVEY, S.

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Free Content Lactase haplotype frequencies in Caucasians: association with the lactase persistence/non-persistence polymorphism
pp. 215-223(9)
Authors: HARVEY, C. B.; HOLLOX, E. J.; POULTER, M.; WANG, Y.; ROSSI, M.; AURICCHIO, S.; IQBAL, T. H.; COOPER, B. T.; BARTON, R.; SARNER, M.; KORPELA, R.; SWALLOW, D. M.

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Free Content C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria
pp. 225-230(6)
Authors: FRANK, J.; WANG, X.; LAM, H-M.; AITA, V. M.; JUGERT, F. K.; GOERZ, G.; MERK, H. F.; POH-FITZPATRICK, M. B.; CHRISTIANO, A. M.

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Free Content Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3–13.4 by an intragenic polymorphic marker
pp. 231-234(4)
Authors: BELLINGHAM, J.; GREGORY-EVANS, K.; GREGORY-EVANS, C. Y.

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Free Content Increased parental age and number of pregnancies in Klippel–Trenaunay–Weber syndrome
pp. 235-239(5)
Authors: LORDA-SANCHEZ, I.; PRIETO, L.; RODRIGUEZ-PINILLA, E.; MARTINEZ-FRÍAS, M. L.

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Free Content Phylogeography of mitochondrial DNA in western Europe
pp. 241-260(20)
Authors: RICHARDS, M. B.; MACAULAY, V. A.; BANDELT, H.-J.; SYKES, B. C.

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Free Content Surnames, HLA genes and ancient migrations in the Po Valley (Italy)
pp. 261-269(9)
Authors: GUGLIELMINO, C. R.; SILVESTRI, A.; ROSSI, A.; MICHELI, V.

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Free Content Identification of a mutation (A1879G) of transferrin from cDNA prepared from peripheral blood cells
pp. 271-274(4)
Authors: PANG, H.; KODA, Y.; SOEJIMA, M.; KIMURA, H.

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