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The New England Journal of Medicine
|
October 26, 1978
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group
L S Levine, M Zachmann, M I New, et al.
Journal of Medical Genetics
|
December 1, 1995
Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting
A Schinzel, I Lorda-Sanchez, F Binkert, et al.
Transplantation Proceedings
|
December 1, 1978
Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group
S Y Yang, L S Levine, M Zachmann, et al.
British Medical Journal
|
March 31, 1973
Familial occurrence of persistent Mullerian structures in otherwise normal males
C G Brook, H Wagner, M Zachmann, et al.
Clinical Endocrinology
|
March 5, 2002
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complications
J Woelfle, W Hoepffner, W G Sippell, et al.
Page
of 17
Search research articles
Search
Showing results (161-170 of 165) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 165 results.
The New England Journal of Medicine
|
October 26, 1978
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group
L S Levine, M Zachmann, M I New, et al.
Journal of Medical Genetics
|
December 1, 1995
Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting
A Schinzel, I Lorda-Sanchez, F Binkert, et al.
Transplantation Proceedings
|
December 1, 1978
Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group
S Y Yang, L S Levine, M Zachmann, et al.
British Medical Journal
|
March 31, 1973
Familial occurrence of persistent Mullerian structures in otherwise normal males
C G Brook, H Wagner, M Zachmann, et al.
Clinical Endocrinology
|
March 5, 2002
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complications
J Woelfle, W Hoepffner, W G Sippell, et al.
Page
of 17