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Blood
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June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene
W C Nichols, K A Cooney, K L Mohlke, et al.
Genomics
|
August 31, 2000
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium
R D Machado, M W Pauciulo, N Fretwell, et al.
Blood
|
March 26, 1999
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency
M Neerman-Arbez, K M Johnson, M A Morris, et al.
Blood
|
September 15, 1995
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene
W C Nichols, K A Cooney, K L Mohlke, et al.
Blood
|
December 15, 1996
Polymorphism of adhesion molecule CD31 is not a significant risk factor for graft-versus-host disease
W C Nichols, J H Antin, K L Lunetta, et al.
Journal of Medical Genetics
|
December 14, 2004
Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension
R Koehler, E Grünig, M W Pauciulo, et al.
Neurology
|
March 13, 2009
Variation in GIGYF2 is not associated with Parkinson disease
W C Nichols, D K Kissell, N Pankratz, et al.
Neurology
|
December 29, 2005
A mutation in myotilin causes spheroid body myopathy
T Foroud, N Pankratz, A P Batchman, et al.
Cell
|
April 18, 1998
Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
W C Nichols, U Seligsohn, A Zivelin, et al.
The New England Journal of Medicine
|
January 1, 1981
Randomized clinical trial of diethylstilbestrol versus tamoxifen in postmenopausal women with advanced breast cancer
J N Ingle, D L Ahmann, S J Green, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Blood
|
June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene
W C Nichols, K A Cooney, K L Mohlke, et al.
Genomics
|
August 31, 2000
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium
R D Machado, M W Pauciulo, N Fretwell, et al.
Blood
|
March 26, 1999
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency
M Neerman-Arbez, K M Johnson, M A Morris, et al.
Blood
|
September 15, 1995
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene
W C Nichols, K A Cooney, K L Mohlke, et al.
Blood
|
December 15, 1996
Polymorphism of adhesion molecule CD31 is not a significant risk factor for graft-versus-host disease
W C Nichols, J H Antin, K L Lunetta, et al.
Journal of Medical Genetics
|
December 14, 2004
Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension
R Koehler, E Grünig, M W Pauciulo, et al.
Neurology
|
March 13, 2009
Variation in GIGYF2 is not associated with Parkinson disease
W C Nichols, D K Kissell, N Pankratz, et al.
Neurology
|
December 29, 2005
A mutation in myotilin causes spheroid body myopathy
T Foroud, N Pankratz, A P Batchman, et al.
Cell
|
April 18, 1998
Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
W C Nichols, U Seligsohn, A Zivelin, et al.
The New England Journal of Medicine
|
January 1, 1981
Randomized clinical trial of diethylstilbestrol versus tamoxifen in postmenopausal women with advanced breast cancer
J N Ingle, D L Ahmann, S J Green, et al.
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of 8