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American Journal of Human Genetics
|
February 11, 1999
Mapping of primary congenital lymphedema to the 5q35.3 region
A L Evans, G Brice, V Sotirova, et al.
Journal of Medical Genetics
|
February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotype
G Brice, A H Child, A Evans, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 1, 1988
Ventilatory and PaCO2 responses to voluntary and electrically induced leg exercise
A G Brice, H V Forster, L G Pan, et al.
Journal of Medical Genetics
|
September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
A L Evans, R Bell, G Brice, et al.
Clinical Genetics
|
January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis
F C Connell, K Kalidas, P Ostergaard, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 1, 1988
Is the hyperpnea of muscular contractions critically dependent on spinal afferents?
A G Brice, H V Forster, L G Pan, et al.
Journal of Medical Genetics
|
August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing
T Aung, N D Ebenezer, G Brice, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
September 1, 1993
Effect of asthma and ventilatory loading on arterial PCO2 of humans during submaximal exercise
H V Forster, M B Dunning, T F Lowry, et al.
Journal of Medical Genetics
|
February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb
R Bell, G Brice, A H Child, et al.
Journal of Medical Genetics
|
December 24, 1998
Novel TIGR/MYOC mutations in families with juvenile onset primary open angle glaucoma
D Stoilova, A Child, G Brice, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
American Journal of Human Genetics
|
February 11, 1999
Mapping of primary congenital lymphedema to the 5q35.3 region
A L Evans, G Brice, V Sotirova, et al.
Journal of Medical Genetics
|
February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotype
G Brice, A H Child, A Evans, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 1, 1988
Ventilatory and PaCO2 responses to voluntary and electrically induced leg exercise
A G Brice, H V Forster, L G Pan, et al.
Journal of Medical Genetics
|
September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
A L Evans, R Bell, G Brice, et al.
Clinical Genetics
|
January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis
F C Connell, K Kalidas, P Ostergaard, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
January 1, 1988
Is the hyperpnea of muscular contractions critically dependent on spinal afferents?
A G Brice, H V Forster, L G Pan, et al.
Journal of Medical Genetics
|
August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing
T Aung, N D Ebenezer, G Brice, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
September 1, 1993
Effect of asthma and ventilatory loading on arterial PCO2 of humans during submaximal exercise
H V Forster, M B Dunning, T F Lowry, et al.
Journal of Medical Genetics
|
February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 Mb
R Bell, G Brice, A H Child, et al.
Journal of Medical Genetics
|
December 24, 1998
Novel TIGR/MYOC mutations in families with juvenile onset primary open angle glaucoma
D Stoilova, A Child, G Brice, et al.
Page
of 6