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American Journal of Medical Genetics
|
August 9, 1996
Slight instability of a FMR-1 allele over three generations in a family from the general population
M J Abramowicz, J Parma, P Cochaux
Journal of Molecular Biology
|
August 20, 1987
Structural organization of the 5' region of the thyroglobulin gene. Evidence for intron loss and "exonization" during evolution
J Parma, D Christophe, V Pohl, et al.
Bulletin of Environmental Contamination and Toxicology
|
August 15, 2002
Inhibition of plasma cholinesterase and acute toxicity of monocrotophos in a neotropical fish Prochilodus lineatus (pisces, curimatidae)
M J Parma De Croux, A Loteste, J Cazenave
Bailliere'S Clinical Endocrinology and Metabolism
|
January 1, 1996
The TSH receptor and thyroid diseases
R Paschke, J Van Sande, J Parma, et al.
Journal of Environmental Biology
|
August 28, 2007
Changes of hematological parameters in Prochilodus lineatus (Pisces, Prochilodontidae) exposed to sublethal concentration of cypermethrin
M J Parma, A Loteste, M Campana, et al.
La Revue Du Praticien
|
December 15, 1994
[Genes, heredity and colorectal cancer]
T Velu, N Ravelingien, J Parma, et al.
European Journal of Endocrinology
|
January 1, 1994
Molecular genetics of thyroid diseases
C Ledent, J Parma, J Dumont, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 24, 2004
Prevalence of germline mutations in the TSH receptor gene as a cause of juvenile thyrotoxicosis
L Lavard, B Brock Jacobsen, H Perrild, et al.
Human Mutation
|
April 11, 2001
A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years
R Demeester, J Parma, P Cochaux, et al.
The Journal of Clinical Investigation
|
June 15, 1997
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland
M J Abramowicz, L Duprez, J Parma, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 69) with videos related to
Sort By:
Page
of 7
American Journal of Medical Genetics
|
August 9, 1996
Slight instability of a FMR-1 allele over three generations in a family from the general population
M J Abramowicz, J Parma, P Cochaux
Journal of Molecular Biology
|
August 20, 1987
Structural organization of the 5' region of the thyroglobulin gene. Evidence for intron loss and "exonization" during evolution
J Parma, D Christophe, V Pohl, et al.
Bulletin of Environmental Contamination and Toxicology
|
August 15, 2002
Inhibition of plasma cholinesterase and acute toxicity of monocrotophos in a neotropical fish Prochilodus lineatus (pisces, curimatidae)
M J Parma De Croux, A Loteste, J Cazenave
Bailliere'S Clinical Endocrinology and Metabolism
|
January 1, 1996
The TSH receptor and thyroid diseases
R Paschke, J Van Sande, J Parma, et al.
Journal of Environmental Biology
|
August 28, 2007
Changes of hematological parameters in Prochilodus lineatus (Pisces, Prochilodontidae) exposed to sublethal concentration of cypermethrin
M J Parma, A Loteste, M Campana, et al.
La Revue Du Praticien
|
December 15, 1994
[Genes, heredity and colorectal cancer]
T Velu, N Ravelingien, J Parma, et al.
European Journal of Endocrinology
|
January 1, 1994
Molecular genetics of thyroid diseases
C Ledent, J Parma, J Dumont, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 24, 2004
Prevalence of germline mutations in the TSH receptor gene as a cause of juvenile thyrotoxicosis
L Lavard, B Brock Jacobsen, H Perrild, et al.
Human Mutation
|
April 11, 2001
A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years
R Demeester, J Parma, P Cochaux, et al.
The Journal of Clinical Investigation
|
June 15, 1997
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland
M J Abramowicz, L Duprez, J Parma, et al.
Page
of 7