Mitochondrial and other enzymes in somatic cell hybrids by Van Heyningen, V

Genetic control of mitochondrial enzymes in human-mouse somatic cell hybrids. by Van Heyningen, V, Craig, I, Bodmer, W

Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and probably, for human... by Van Heyningen, V, Bobrow, M, Bodmer, W

Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human... by van Heyningen, V, Bobrow, M, Bodmer, W, Povey, S, Gardiner, SE, Hopkinson, D

Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13. by van Heyningen, V, Bobrow, M, Bodmer, W, Gardiner, SE, Povey, S, Hopkinson, D

Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human... by van Heyningen, V, Bobrow, M, Bodmer, W, Povey, S, Gardiner, SE, Hopkinson, D

Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus. by Pang, J, Pook, M, Eubanks, J, Jones, C, van Heyningen, V, Evans, G, Thakker, R

The beta2-microglobulin gene is on chromosome 15 and not in the HL-A region. by Goodfellow, P, Jones, E, Van Heyningen, V, Solomon, E, Bobrow, M, Miggiano, V, Bodmer, W

Linkage relationships of the HL-A system and beta 2 microglobulin. by Goodfellow, P, Jones, E, van Heyningen, V, Solomon, E, Kennett, R, Bobrow, M, Bodmer, W

Linkage relationships of the HL-A system and beta2 microglobulin. by Goodfellow, P, Jones, E, van Heyningen, V, Solomon, E, Kennett, R, Bobrow, M, Bodmer, W

The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis by Sansom, S, Griffiths, D, Faedo, A, Kleinjan, D, Ruan, Y, Smith, J, Van Heyningen, V, Rubenstein, J, Livesey, F

EagI and NotI linking clones from human chromosomes 11 and Xp. by Pook, M, Thakrar, R, Pottinger, B, Harding, B, Porteous, D, van Heyningen, V, Cowell, J, Jones, C, Povey, S, Davies, K, Thakker, R

Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. by Williamson, K, Rainger, J, Floyd, J, Ansari, M, Meynert, A, Aldridge, K, Rainger, J, Anderson, C, Moore, A, Hurles, M, Clarke, A, van Heyningen, V, Verloes, A, Taylor, MS, Wilkie, A, Fitzpatrick, DR