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Journal of Medical Genetics
|
June 1, 1994
Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?
C Eng, V Murday, S Seal, et al.
Human Molecular Genetics
|
November 1, 1995
The mutational spectrum in Waardenburg syndrome
M Tassabehji, V E Newton, X Z Liu, et al.
British Journal of Cancer
|
August 12, 2004
A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes
P Hopwood, D Wonderling, M Watson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli
L Varesco, H J Thomas, S Cottrell, et al.
Scottish Medical Journal
|
November 18, 2011
Impact of national guidelines on family history breast cancer surveillance
J D Saldanha, R M Garrett, L Snaddon, et al.
Journal of Medical Genetics
|
April 4, 2006
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
N C M Hearle, M F Rudd, W Lim, et al.
American Journal of Human Genetics
|
October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
M A Simpson, R Hsu, L S Keir, et al.
British Journal of Cancer
|
July 17, 2003
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome
W Lim, N Hearle, B Shah, et al.
British Journal of Cancer
|
February 20, 2008
Prospective surveillance of women with a family history of breast cancer: auditing the risk threshold
E Anderson, J Berg, R Black, et al.
Human Mutation
|
November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome
V Laugel, C Dalloz, M Durand, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Journal of Medical Genetics
|
June 1, 1994
Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?
C Eng, V Murday, S Seal, et al.
Human Molecular Genetics
|
November 1, 1995
The mutational spectrum in Waardenburg syndrome
M Tassabehji, V E Newton, X Z Liu, et al.
British Journal of Cancer
|
August 12, 2004
A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes
P Hopwood, D Wonderling, M Watson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli
L Varesco, H J Thomas, S Cottrell, et al.
Scottish Medical Journal
|
November 18, 2011
Impact of national guidelines on family history breast cancer surveillance
J D Saldanha, R M Garrett, L Snaddon, et al.
Journal of Medical Genetics
|
April 4, 2006
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
N C M Hearle, M F Rudd, W Lim, et al.
American Journal of Human Genetics
|
October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
M A Simpson, R Hsu, L S Keir, et al.
British Journal of Cancer
|
July 17, 2003
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome
W Lim, N Hearle, B Shah, et al.
British Journal of Cancer
|
February 20, 2008
Prospective surveillance of women with a family history of breast cancer: auditing the risk threshold
E Anderson, J Berg, R Black, et al.
Human Mutation
|
November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome
V Laugel, C Dalloz, M Durand, et al.
Page
of 3