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pro vyhledávání: '"Belinda Petrovic"'
Autor:
Jason J. Bisaillon, Legairre A. Radden II, Eric T. Szabo, Samantha R. Hughes, Aaron M. Feliciano, Alex V. Nesta, Belinda Petrovic, Kenneth M. Palanza, Dainius Lancinskas, Theodore A. Szmurlo, David C. Artus, Martin A. Kapper, James P. Mulrooney, Thomas R. King
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Because of the similar phenotypes they generate and their proximate reported locations on Chromosome 7, we tested the recessive retarded hair growth (rhg) and frizzy (fr) mouse mutations for allelism, but found instead that these defects complement.
Externí odkaz:
https://doaj.org/article/9efcf5e7a54343e2a3afd8cd858106f1
Autor:
Belinda Petrovic, David C. Artus, Dainius Lancinskas, Samantha R. Hughes, Legairre A. Radden, Eric T. Szabo, Martin A. Kapper, Jason J. Bisaillon, James P. Mulrooney, Aaron M Feliciano, Alex V. Nesta, Kenneth M. Palanza, Theodore A. Szmurlo, Thomas R. King
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Because of the similar phenotypes they generate and their proximate reported locations on Chromosome 7, we tested the recessive retarded hair growth (rhg) and frizzy (fr) mouse mutations for allelism, but found instead that these defects complement.