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Journal of Medical Genetics
|
October 12, 2001
Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions
P Syrris, A Murray, N D Carter, et al.
Clinical Genetics
|
May 8, 2010
A new classification system for primary lymphatic dysplasias based on phenotype
F Connell, G Brice, S Jeffery, et al.
Lancet (London, England)
|
December 20, 1980
Amniotic fluid carbonic anhydrase III not a predictor of Duchenne dystrophy
N D Carter, R Heath, S Jeffery, et al.
The Journal of Infectious Diseases
|
May 1, 1990
Prostatitis caused by Hansenula fabianii
D P Dooley, M L Beckius, C K McAllister, et al.
Journal of Medical Genetics
|
February 25, 1998
Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease
K D MacDermot, A K Saggar-Malik, D L Economides, et al.
Clinical Genetics
|
January 26, 2007
Three children with Milroy disease and de novo mutations in VEGFR3
C Carver, G Brice, S Mansour, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
January 1, 1982
Zinc and carbonic anhydrase III distribution in mammalian muscle
D Jeffery, Y H Edwards, M J Jackson, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
April 4, 2000
The impact of a pregnancy confirmation clinic on the commencement of antenatal care
B S Jeffery, M Tsuari, L R Pistorius, et al.
FEBS Letters
|
March 26, 1990
Chronic stimulation-induced effects point to a coordinated expression of carbonic anhydrase III and slow myosin heavy chain in skeletal muscle
S Jeffery, C D Kelly, N Carter, et al.
Journal of Human Hypertension
|
June 1, 1996
Factor V Leiden polymorphism (FV Q506) in patients with ischaemic heart disease, and in different populations groups
S Jeffery, E Leatham, Y Zhang, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 181) with videos related to
Sort By:
Page
of 19
Journal of Medical Genetics
|
October 12, 2001
Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions
P Syrris, A Murray, N D Carter, et al.
Clinical Genetics
|
May 8, 2010
A new classification system for primary lymphatic dysplasias based on phenotype
F Connell, G Brice, S Jeffery, et al.
Lancet (London, England)
|
December 20, 1980
Amniotic fluid carbonic anhydrase III not a predictor of Duchenne dystrophy
N D Carter, R Heath, S Jeffery, et al.
The Journal of Infectious Diseases
|
May 1, 1990
Prostatitis caused by Hansenula fabianii
D P Dooley, M L Beckius, C K McAllister, et al.
Journal of Medical Genetics
|
February 25, 1998
Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease
K D MacDermot, A K Saggar-Malik, D L Economides, et al.
Clinical Genetics
|
January 26, 2007
Three children with Milroy disease and de novo mutations in VEGFR3
C Carver, G Brice, S Mansour, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
January 1, 1982
Zinc and carbonic anhydrase III distribution in mammalian muscle
D Jeffery, Y H Edwards, M J Jackson, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
April 4, 2000
The impact of a pregnancy confirmation clinic on the commencement of antenatal care
B S Jeffery, M Tsuari, L R Pistorius, et al.
FEBS Letters
|
March 26, 1990
Chronic stimulation-induced effects point to a coordinated expression of carbonic anhydrase III and slow myosin heavy chain in skeletal muscle
S Jeffery, C D Kelly, N Carter, et al.
Journal of Human Hypertension
|
June 1, 1996
Factor V Leiden polymorphism (FV Q506) in patients with ischaemic heart disease, and in different populations groups
S Jeffery, E Leatham, Y Zhang, et al.
Page
of 19