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Showing results (171-180 of 174) with videos related to

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Blood|December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
T. Brookhaven National Laboratory|February 19, 2014
Medical survey of Rongelap people five and six years after exposure to fallout (with an addendum on vegetation)R A CONARD, H E MACDONALD, A LOWREY, et al.
Nature Genetics|January 28, 2003
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6Qing Zhang, Baohui Zhao, Wei Li, et al.
Pageof 18

Showing results (171-180 of 174) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 174 results.
Blood|December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
T. Brookhaven National Laboratory|February 19, 2014
Medical survey of Rongelap people five and six years after exposure to fallout (with an addendum on vegetation)R A CONARD, H E MACDONALD, A LOWREY, et al.
Nature Genetics|January 28, 2003
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6Qing Zhang, Baohui Zhao, Wei Li, et al.
Pageof 18