论文信息 - Autosomal Deletion Mapping in Man

Autosomal Deletion Mapping in Man

Two families were observed in which morphologically similar dele tions involving a G-group chromosome were associated in the propositi with con spicuous abnormalities in ossification of the skull. The findings suggest that specific genetic information relating to morphogenesis of the skull may be located on a G-group chromosome.

W. Nance | E. Engel | Walter E. Nance

[1] W. Nance,et al. Pycnodysostosis, with a familial chromosome anomaly. , 1966, The American journal of medicine.

[2] V. McKusick. GENERALIZED GENETIC DISORDERS OF THE OSSEOUS SKELETON. , 1965, JAMA.

[3] J. Changeux,et al. Allosteric proteins and cellular control systems. , 1963, Journal of molecular biology.

[4] N. Franklin,et al. Transduction by bacteriophage P-1 and the properties of the lac genetic region in E. coli and S. dysenteriae. , 1961, Virology.

[5] J. Monod,et al. Genetic regulatory mechanisms in the synthesis of proteins. , 1961, Journal of molecular biology.

[6] P. Nowell,et al. Chromosome preparations of leukocytes cultured from human peripheral blood. , 1960, Experimental cell research.

[7] S. Benzer,et al. FINE STRUCTURE OF A GENETIC REGION IN BACTERIOPHAGE. , 1955, Proceedings of the National Academy of Sciences of the United States of America.

[8] H. Muller. A VIABLE TWO-GENE DEFICIENCYPhaenotypically Resenbling the Corresponding Hypomorphic Mutations , 1935 .

[9] O. Smithies. CHROMOSOMAL REARRANGEMENTS AND PROTEIN STRUCTURE. , 1964, Cold Spring Harbor symposia on quantitative biology.

[10] N. Talal,et al. Protein Structure and Biological Regulation , 1963 .

[11] B. Ames,et al. The Histidine Operon , 1963 .