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P J Mason

Showing results (41-50 of 80) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 1, 1996
Unproductive folding of the human G6PD-deficient variant A-F Gómez-Gallego, A Garrido-Pertierra, P J Mason, et al.
Cell|July 13, 1990
Human red cell glucose-6-phosphate dehydrogenase is encoded only on the X chromosomeP J Mason, J M Bautista, T J Vulliamy, et al.
Nucleic Acids Research|December 11, 1990
G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutationD J Stevens, W Wanachiwanawin, P J Mason, et al.
Leukemia|October 1, 1995
A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a reviewD Macdonald, R C Aguiar, P J Mason, et al.
Blood|July 15, 1995
Myeloproliferative disorder associated with 8p11 translocationsR C Aguiar, D Macdonald, P J Mason, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 1998
Sequence analysis of the 'Goodpasture antigen' of mammalsJ J Ryan, I Katbamna, P J Mason, et al.
Journal of Pediatric Psychology|September 1, 1989
AIDS and hemophilia: implications for interventions with familiesP J Mason, R A Olson, J G Myers, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 1, 1996
Unproductive folding of the human G6PD-deficient variant A-F Gómez-Gallego, A Garrido-Pertierra, P J Mason, et al.
Cell|July 13, 1990
Human red cell glucose-6-phosphate dehydrogenase is encoded only on the X chromosomeP J Mason, J M Bautista, T J Vulliamy, et al.
Nucleic Acids Research|December 11, 1990
G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutationD J Stevens, W Wanachiwanawin, P J Mason, et al.
Leukemia|October 1, 1995
A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a reviewD Macdonald, R C Aguiar, P J Mason, et al.
Blood|July 15, 1995
Myeloproliferative disorder associated with 8p11 translocationsR C Aguiar, D Macdonald, P J Mason, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 1998
Sequence analysis of the 'Goodpasture antigen' of mammalsJ J Ryan, I Katbamna, P J Mason, et al.
Journal of Pediatric Psychology|September 1, 1989
AIDS and hemophilia: implications for interventions with familiesP J Mason, R A Olson, J G Myers, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
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