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La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
October 9, 1977
[Evaluation of the results of treatment of Graves' disease by synthetic antithyroid drugs]
D Fischer, J Poncin, R Dunet, et al.
Human Genetics
|
September 1, 1990
Prevalence of the delta F508 deletion of the cystic fibrosis gene in Belgian patients
P Cochaux, R van Geffel, D Baran, et al.
Acta Gastro-Enterologica Belgica
|
March 1, 1979
[Cystadenoma of the pancreas. Case report (author's transl)]
J Poncin, M Deschreyer, J P Serste, et al.
The Journal of Pathology
|
November 26, 1998
APC mutations in human colorectal adenomas: analysis of the mutation cluster region with temperature gradient gel electrophoresis and clinicopathological features
J Mulkens, J Poncin, J W Arends, et al.
Annales De Medecine Interne
|
January 1, 1984
[Diagnostic value of the determination of nephrogenic cyclic AMP, and the value of cervical echography for localization in primary hyperparathyroidism. 13 cases]
M Bentata-Pessayre, A Krivitzky, B Fond, et al.
Biochemical and Biophysical Research Communications
|
April 7, 1997
Luteinizing hormone increases the abundance of various transcripts, independently of the androgens, in the rat prostate
E Reiter, J Poncin, B Hennuy, et al.
Endocrinology
|
September 28, 1999
A novel gene overexpressed in the prostate of castrated rats: hormonal regulation, relationship to apoptosis and to acquired prostatic cell androgen independence
M Bruyninx, B Hennuy, A Cornet, et al.
American Journal of Human Genetics
|
June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis
B D Gelb, J P Willner, T M Dunn, et al.
American Journal of Human Genetics
|
May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2
V Biancalana, M L Briard, A David, et al.
Human Mutation
|
January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
J Poncin, R Abs, B Velkeniers, et al.
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of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
October 9, 1977
[Evaluation of the results of treatment of Graves' disease by synthetic antithyroid drugs]
D Fischer, J Poncin, R Dunet, et al.
Human Genetics
|
September 1, 1990
Prevalence of the delta F508 deletion of the cystic fibrosis gene in Belgian patients
P Cochaux, R van Geffel, D Baran, et al.
Acta Gastro-Enterologica Belgica
|
March 1, 1979
[Cystadenoma of the pancreas. Case report (author's transl)]
J Poncin, M Deschreyer, J P Serste, et al.
The Journal of Pathology
|
November 26, 1998
APC mutations in human colorectal adenomas: analysis of the mutation cluster region with temperature gradient gel electrophoresis and clinicopathological features
J Mulkens, J Poncin, J W Arends, et al.
Annales De Medecine Interne
|
January 1, 1984
[Diagnostic value of the determination of nephrogenic cyclic AMP, and the value of cervical echography for localization in primary hyperparathyroidism. 13 cases]
M Bentata-Pessayre, A Krivitzky, B Fond, et al.
Biochemical and Biophysical Research Communications
|
April 7, 1997
Luteinizing hormone increases the abundance of various transcripts, independently of the androgens, in the rat prostate
E Reiter, J Poncin, B Hennuy, et al.
Endocrinology
|
September 28, 1999
A novel gene overexpressed in the prostate of castrated rats: hormonal regulation, relationship to apoptosis and to acquired prostatic cell androgen independence
M Bruyninx, B Hennuy, A Cornet, et al.
American Journal of Human Genetics
|
June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis
B D Gelb, J P Willner, T M Dunn, et al.
American Journal of Human Genetics
|
May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2
V Biancalana, M L Briard, A David, et al.
Human Mutation
|
January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
J Poncin, R Abs, B Velkeniers, et al.
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of 2