Research Article
Molecular cloning, functional characterization and genomic organization of four alternatively spliced isoforms of the human organic cation transporter 1 (hOCT1/SLC22A1)
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- 01 November 1999, pp. 473-482
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Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese
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- 01 November 1999, pp. 483-487
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Molecular instability of the mitochondrial haplogroup T sequences at nucleotide positions 16292 and 16296
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- 01 November 1999, pp. 489-497
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Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci
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- 01 November 1999, pp. 499-510
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Linking genotype to aorto-coronary atherosclerosis: a model using familial hypercholesterolemia and aorto-coronary calcification
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- 01 November 1999, pp. 511-520
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Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene
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- 01 November 1999, pp. 521-533
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Hardy–Weinberg quality control
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- 01 November 1999, pp. 535-538
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Familial association of disease and the structure of trivariate distributions
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- 01 November 1999, pp. 539-544
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Power of variance component linkage analysis to detect quantitative trait loci
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- 01 November 1999, pp. 545-563
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Book Review
Inherited Skin Disorders: The Genodermatoses. Edited by J. HARPER (Genetics Advisor: M. Pembrey; Illustrative Editor: S. Brown). Oxford: Butterworth/Heinemann. 1999 (1st hardback edition published 1996). Pp. 355. £49.50 (paperback).
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- 01 November 1999, p. 567
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