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Number of items: 3.

B

Bartoloni, L. and Blouin, J.L. and Maiti, A.K. and Sainsbury, A. and Rossier, C. and Gehrig, C. and She, J.X. and Marron, M.P. and Lander, E.S. and Meeks, M. and Chung, E. and Armengot, M. and Jorissen, M. and Scott, H.S. and Delozier-Blanchet, C.D. and Gardiner, R.M. and Antonarakis, S.E. (2001) Axonnemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia. Genomics , 72 (1) pp. 21-33. 10.1006/geno.2000.6462.

M

Mitchell, W.A. and Wheeler, R.B. and Sharp, J.D. and Bate, S.L. and Gardiner, R.M. and Ranta, U.S. and Lonka, L. and Williams, R.E. and Lehesjoki, A.-E. and Mole, S.E. (2001) Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8. European Journal of Paediatric Neurology , 5 (Supplement A) pp. 21-27.

S

Sharp, J.D. and Wheeler, R.B. and Schultz, R.A. and Joslin, J.M. and Mole, S.E. and Williams, R.E. and Gardiner, R.M. (2001) Analysis of candidate genes in the CLN6 critical region using in silico cloning. European Journal of Paediatric Neurology , 5 (Supplement A) pp. 29-31.

This list was generated on Tue May 21 13:53:44 2013 BST.