2002 William Allen Award address. Introductory speech for Albert de la Chapelle.
暂无分享,去创建一个
[1] A. de la Chapelle,et al. Apparent C trisomy in bone marrow cells. Report of two cases. , 2009, Scandinavian journal of haematology.
[2] M. Niemi,et al. XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE. , 2009, Acta medica Scandinavica.
[3] Bo Yuan,et al. Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. , 2001, American journal of human genetics.
[4] A. Chapelle,et al. Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia , 2001, Cell.
[5] A. Chapelle,et al. The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8 , 1999, Nature Genetics.
[6] F. Wright,et al. Linkage disequilibrium mapping in isolated populations: the example of Finland revisited. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[7] A. Chapelle,et al. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure , 1995, Cell.
[8] Eric S. Lander,et al. The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping , 1994, Cell.
[9] A. Chapelle,et al. Disease gene mapping in isolated human populations: the example of Finland. , 1993, Journal of medical genetics.
[10] K. Kinzler,et al. Clues to the pathogenesis of familial colorectal cancer. , 1993, Science.
[11] D. Page,et al. Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males , 1986, Science.
[12] J. Weissenbach,et al. Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes , 1985, Nature.
[13] J. Weissenbach,et al. Chromosome Y-specific DNA in related human XX males , 1985, Nature.
[14] A. Chapelle,et al. Genetic evidence of X–Y interchange in a human XX male , 1984, Nature.
[15] A. de la Chapelle,et al. Mapping of the gene for glutathione reductase on chromosome 8. , 1976, Annales de genetique.
[16] A. Chapelle,et al. 8‐trisomy in the bone marrow. Report of two cases , 1972, Clinical genetics.
[17] Peter Beighton,et al. de la Chapelle, A. , 1997 .
[18] L. Brown,et al. Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males , 1987, Nature.