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Human Genetics
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December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosis
M C Romey, P Aguilar-Martinez, J Demaille, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1990
[Male pseudo-hermaphroditism. Prenatal factors]
P Aguilar-Martinez, F Montoya, P Montoya, et al.
Blood
|
September 1, 1996
A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome
P Aguilar-Martinez, C Biron, C Masmejean, et al.
Presse Medicale (Paris, France : 1983)
|
February 23, 1991
[Endothelial mediators regulating vascular tonus]
J C Gris, J F Schved, P Aguilar-Martinez, et al.
Presse Medicale (Paris, France : 1983)
|
July 6, 1991
[Recurrent venous thromboembolism caused by heparin cofactor II deficiency. A case]
J F Schved, J C Gris, P Aguilar-Martinez, et al.
Blood Cells, Molecules & Diseases
|
November 27, 1999
Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations
P Aguilar-Martinez, C Thelcide, P Jeanjean, et al.
Dermatology (Basel, Switzerland)
|
April 9, 2002
No evidence of Y250X transferrin receptor type 2 mutation in patients with porphyria cutanea tarda. A study of 38 cases
O Dereure, C Esculier, P Aguilar-Martinez, et al.
British Journal of Haematology
|
February 13, 2001
Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome
M Giansily, C Beaumont, C Desveaux, et al.
Annales De Medecine Interne
|
January 1, 1993
[Prevalence of minor beta-thalassemia in the region of Gard]
C Maugard, P Aguilar-Martinez, J C Gris, et al.
Prenatal Diagnosis
|
November 1, 1992
Potential co-existence of haemophilia A and B carrier status in two sisters
P Aguilar-Martinez, R Navarro, J F Schved, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Human Genetics
|
December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosis
M C Romey, P Aguilar-Martinez, J Demaille, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1990
[Male pseudo-hermaphroditism. Prenatal factors]
P Aguilar-Martinez, F Montoya, P Montoya, et al.
Blood
|
September 1, 1996
A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome
P Aguilar-Martinez, C Biron, C Masmejean, et al.
Presse Medicale (Paris, France : 1983)
|
February 23, 1991
[Endothelial mediators regulating vascular tonus]
J C Gris, J F Schved, P Aguilar-Martinez, et al.
Presse Medicale (Paris, France : 1983)
|
July 6, 1991
[Recurrent venous thromboembolism caused by heparin cofactor II deficiency. A case]
J F Schved, J C Gris, P Aguilar-Martinez, et al.
Blood Cells, Molecules & Diseases
|
November 27, 1999
Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations
P Aguilar-Martinez, C Thelcide, P Jeanjean, et al.
Dermatology (Basel, Switzerland)
|
April 9, 2002
No evidence of Y250X transferrin receptor type 2 mutation in patients with porphyria cutanea tarda. A study of 38 cases
O Dereure, C Esculier, P Aguilar-Martinez, et al.
British Journal of Haematology
|
February 13, 2001
Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome
M Giansily, C Beaumont, C Desveaux, et al.
Annales De Medecine Interne
|
January 1, 1993
[Prevalence of minor beta-thalassemia in the region of Gard]
C Maugard, P Aguilar-Martinez, J C Gris, et al.
Prenatal Diagnosis
|
November 1, 1992
Potential co-existence of haemophilia A and B carrier status in two sisters
P Aguilar-Martinez, R Navarro, J F Schved, et al.
Page
of 4