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Circulation
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March 1, 1994
Blood pressure and endocrine responses to changes in dietary sodium intake in cardiac transplant recipients. Implications for the control of sodium balance
D R Singer, N D Markandu, M G Buckley, et al.
Familial Cancer
|
October 24, 2003
Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?
L Lipton, H J Thomas, R A Eeles, et al.
Human Genetics
|
August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene
R Bell, G Brice, A H Child, et al.
Journal of Medical Genetics
|
December 1, 1998
Germline PTEN mutations in Cowden syndrome-like families
D J Marsh, P L Dahia, S Caron, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 24, 2004
Comparison of survival following coronary artery bypass grafting vs. percutaneous coronary intervention in diabetic and non-diabetic patients: retrospective cohort study of 6320 procedures
J P Pell, A C H Pell, R R Jeffrey, et al.
American Journal of Human Genetics
|
April 1, 1996
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q
H J Thomas, S C Whitelaw, S E Cottrell, et al.
Gastroenterology
|
February 1, 1997
Clinical and molecular features of the hereditary mixed polyposis syndrome
S C Whitelaw, V A Murday, I P Tomlinson, et al.
American Journal of Human Genetics
|
July 27, 1999
A gene for lymphedema-distichiasis maps to 16q24.3
J Mangion, N Rahman, S Mansour, et al.
Nature Genetics
|
September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
American Journal of Human Genetics
|
April 16, 2003
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
E E M Jaeger, K L Woodford-Richens, M Lockett, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Circulation
|
March 1, 1994
Blood pressure and endocrine responses to changes in dietary sodium intake in cardiac transplant recipients. Implications for the control of sodium balance
D R Singer, N D Markandu, M G Buckley, et al.
Familial Cancer
|
October 24, 2003
Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?
L Lipton, H J Thomas, R A Eeles, et al.
Human Genetics
|
August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene
R Bell, G Brice, A H Child, et al.
Journal of Medical Genetics
|
December 1, 1998
Germline PTEN mutations in Cowden syndrome-like families
D J Marsh, P L Dahia, S Caron, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 24, 2004
Comparison of survival following coronary artery bypass grafting vs. percutaneous coronary intervention in diabetic and non-diabetic patients: retrospective cohort study of 6320 procedures
J P Pell, A C H Pell, R R Jeffrey, et al.
American Journal of Human Genetics
|
April 1, 1996
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q
H J Thomas, S C Whitelaw, S E Cottrell, et al.
Gastroenterology
|
February 1, 1997
Clinical and molecular features of the hereditary mixed polyposis syndrome
S C Whitelaw, V A Murday, I P Tomlinson, et al.
American Journal of Human Genetics
|
July 27, 1999
A gene for lymphedema-distichiasis maps to 16q24.3
J Mangion, N Rahman, S Mansour, et al.
Nature Genetics
|
September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
American Journal of Human Genetics
|
April 16, 2003
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
E E M Jaeger, K L Woodford-Richens, M Lockett, et al.
Page
of 7