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Journal of Medical Genetics
|
April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
H L Archer, J Evans, S Edwards, et al.
Journal of Medical Genetics
|
June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome
S Lindsay, M Ireland, O O'Brien, et al.
Journal of Genetic Counseling
|
July 5, 2015
Genetic Testing Considerations in Breast Cancer Patients
L France, J Gray, G Elwyn, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 19, 2005
A mobile screening programme for the cardiovascular and microvascular complications of Type 2 diabetes in primary care
M J Sampson, P Barrie, N Dozio, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 19, 2010
Cord blood telomere length, telomerase activity and inflammatory markers in pregnancies in women with diabetes or gestational diabetes
J A Cross, R C Temple, J C Hughes, et al.
Environmental Health Perspectives
|
October 26, 2000
Levels of seven urinary phthalate metabolites in a human reference population
B C Blount, M J Silva, S P Caudill, et al.
The Journal of Heredity
|
February 13, 1999
Use of cosmid-derived and chromosome-specific canine microsatellites
H F Dickens, N G Holmes, E Ryder, et al.
Biological Trace Element Research
|
April 26, 2003
Serum selenium levels in the US population: Third National Health and Nutrition Examination Survey, 1988-1994
Amanda S Niskar, Daniel C Paschal, Stephanie M Kieszak, et al.
Archives of Environmental Contamination and Toxicology
|
July 1, 1993
Contaminants in L-tryptophan associated with eosinophilia myalgia syndrome
R H Hill, S P Caudill, R M Philen, et al.
International Journal of Systematic and Evolutionary Microbiology
|
July 11, 2006
Enterococcus caccae sp. nov., isolated from human stools
Maria da Glória S Carvalho, P Lynn Shewmaker, Arnold G Steigerwalt, et al.
Page
of 42
Search research articles
Search
Showing results (351-360 of 411) with videos related to
Sort By:
Page
of 42
Journal of Medical Genetics
|
April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients
H L Archer, J Evans, S Edwards, et al.
Journal of Medical Genetics
|
June 1, 1997
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome
S Lindsay, M Ireland, O O'Brien, et al.
Journal of Genetic Counseling
|
July 5, 2015
Genetic Testing Considerations in Breast Cancer Patients
L France, J Gray, G Elwyn, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 19, 2005
A mobile screening programme for the cardiovascular and microvascular complications of Type 2 diabetes in primary care
M J Sampson, P Barrie, N Dozio, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 19, 2010
Cord blood telomere length, telomerase activity and inflammatory markers in pregnancies in women with diabetes or gestational diabetes
J A Cross, R C Temple, J C Hughes, et al.
Environmental Health Perspectives
|
October 26, 2000
Levels of seven urinary phthalate metabolites in a human reference population
B C Blount, M J Silva, S P Caudill, et al.
The Journal of Heredity
|
February 13, 1999
Use of cosmid-derived and chromosome-specific canine microsatellites
H F Dickens, N G Holmes, E Ryder, et al.
Biological Trace Element Research
|
April 26, 2003
Serum selenium levels in the US population: Third National Health and Nutrition Examination Survey, 1988-1994
Amanda S Niskar, Daniel C Paschal, Stephanie M Kieszak, et al.
Archives of Environmental Contamination and Toxicology
|
July 1, 1993
Contaminants in L-tryptophan associated with eosinophilia myalgia syndrome
R H Hill, S P Caudill, R M Philen, et al.
International Journal of Systematic and Evolutionary Microbiology
|
July 11, 2006
Enterococcus caccae sp. nov., isolated from human stools
Maria da Glória S Carvalho, P Lynn Shewmaker, Arnold G Steigerwalt, et al.
Page
of 42