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Journal of Medical Genetics
|
March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies
M A Patton, F Giannelli, A J Francis, et al.
Developmental Medicine and Child Neurology
|
February 1, 1997
Agenesis of the corpus callosum in Turner syndrome with ring X
S E Abd, L Wilson, P Howlin, et al.
Genetic Testing
|
February 24, 2001
Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversion
A R Afzal, R N FlorĂȘncio, R Taylor, et al.
Journal of Medical Genetics
|
May 1, 1990
Restrictive dermopathy: a report of three cases
Q Mok, R Curley, J L Tolmie, et al.
Journal of Dairy Science
|
February 23, 2008
Effect of supplementing rumen-protected methionine on production and nitrogen excretion in lactating dairy cows
G A Broderick, M J Stevenson, R A Patton, et al.
Journal of Medical Genetics
|
April 16, 1998
Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestation
A F Brady, P P Pandya, B Yuksel, et al.
The Journal of Biological Chemistry
|
June 23, 1998
Phospholipid- and GTP-dependent activation of cholera toxin and phospholipase D by human ADP-ribosylation factor-like protein 1 (HARL1)
J X Hong, F J Lee, W A Patton, et al.
British Heart Journal
|
December 1, 1992
Myocardial disarray in Noonan syndrome
M Burch, J M Mann, M Sharland, et al.
The British Journal of Dermatology
|
April 12, 2001
Homozygosity at chromosome 8qter in individuals affected by mal de Meleda (Meleda disease) originating from the island of Meleda
H Patel, M Nardelli, T Fenn, et al.
Work (Reading, Mass.)
|
June 16, 2011
Evaluation of anti-vibration interventions for the hand during sheet metal assembly work
Ann Marie Dale, A E Rohn, A Burwell, et al.
Page
of 42
Search research articles
Search
Showing results (251-260 of 412) with videos related to
Sort By:
Page
of 42
Journal of Medical Genetics
|
March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies
M A Patton, F Giannelli, A J Francis, et al.
Developmental Medicine and Child Neurology
|
February 1, 1997
Agenesis of the corpus callosum in Turner syndrome with ring X
S E Abd, L Wilson, P Howlin, et al.
Genetic Testing
|
February 24, 2001
Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversion
A R Afzal, R N FlorĂȘncio, R Taylor, et al.
Journal of Medical Genetics
|
May 1, 1990
Restrictive dermopathy: a report of three cases
Q Mok, R Curley, J L Tolmie, et al.
Journal of Dairy Science
|
February 23, 2008
Effect of supplementing rumen-protected methionine on production and nitrogen excretion in lactating dairy cows
G A Broderick, M J Stevenson, R A Patton, et al.
Journal of Medical Genetics
|
April 16, 1998
Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestation
A F Brady, P P Pandya, B Yuksel, et al.
The Journal of Biological Chemistry
|
June 23, 1998
Phospholipid- and GTP-dependent activation of cholera toxin and phospholipase D by human ADP-ribosylation factor-like protein 1 (HARL1)
J X Hong, F J Lee, W A Patton, et al.
British Heart Journal
|
December 1, 1992
Myocardial disarray in Noonan syndrome
M Burch, J M Mann, M Sharland, et al.
The British Journal of Dermatology
|
April 12, 2001
Homozygosity at chromosome 8qter in individuals affected by mal de Meleda (Meleda disease) originating from the island of Meleda
H Patel, M Nardelli, T Fenn, et al.
Work (Reading, Mass.)
|
June 16, 2011
Evaluation of anti-vibration interventions for the hand during sheet metal assembly work
Ann Marie Dale, A E Rohn, A Burwell, et al.
Page
of 42