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Human Mutation
|
October 26, 1999
Protein truncation test for screening hamartin gene mutations and report of new disease-causing mutations
P Bénit, A Kara-Mostefa, S Hadj-Rabia, et al.
Human Mutation
|
November 3, 2000
Mutation analysis of the hamartin gene using denaturing high performance liquid chromatography
P Bénit, A Kara-Mostefa, M Berthelon, et al.
The Annals of Thoracic Surgery
|
June 5, 2001
Effect of ethanol and ether in the prevention of calcification of bioprostheses
M Shen, A Kara-Mostefa, L Chen, et al.
Prenatal Diagnosis
|
April 5, 2001
Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis
P Bénit, J P Bonnefont, A Kara Mostefa, et al.
Virologie (Montrouge, France)
|
November 4, 2021
[HIV1 group O: diagnostic difficulties]
A Kara-Mostefa, V Schneider, C Amiel, et al.
American Journal of Human Genetics
|
April 17, 1999
Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism
A Kara-Mostefa, O Raoul, S Lyonnet, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Human Mutation
|
October 26, 1999
Protein truncation test for screening hamartin gene mutations and report of new disease-causing mutations
P Bénit, A Kara-Mostefa, S Hadj-Rabia, et al.
Human Mutation
|
November 3, 2000
Mutation analysis of the hamartin gene using denaturing high performance liquid chromatography
P Bénit, A Kara-Mostefa, M Berthelon, et al.
The Annals of Thoracic Surgery
|
June 5, 2001
Effect of ethanol and ether in the prevention of calcification of bioprostheses
M Shen, A Kara-Mostefa, L Chen, et al.
Prenatal Diagnosis
|
April 5, 2001
Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis
P Bénit, J P Bonnefont, A Kara Mostefa, et al.
Virologie (Montrouge, France)
|
November 4, 2021
[HIV1 group O: diagnostic difficulties]
A Kara-Mostefa, V Schneider, C Amiel, et al.
American Journal of Human Genetics
|
April 17, 1999
Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism
A Kara-Mostefa, O Raoul, S Lyonnet, et al.
Page
of 1