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Molecular Human Reproduction
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June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy
A Girardet, S Hamamah, H Déchaud, et al.
Molecular Human Reproduction
|
September 13, 2003
Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting
T Anahory, B Andréo, G Régnier-Vigouroux, et al.
Human Genetics
|
December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies
M Claustres, S Tuffery, M P Chevron, et al.
Human Mutation
|
January 1, 1994
A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patient
P Aguilar-Martinez, M C Romey, J C Gris, et al.
Human Genetics
|
September 1, 1994
Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applications
P Aguilar-Martinez, M C Romey, J F Schved, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies
C F Schmitt-Bernard, C Guittard, B Arnaud, et al.
Annals of Hematology
|
May 1, 1993
Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patient
P Aguilar-Martinez, F Galacteros, J F Schved, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Direct carrier detection for severe haemophilia A: application to families with no available affected male
C Maugard, P Aguilar-Martinez, J F Schved, et al.
Genetic Testing
|
April 19, 2002
Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness
N Pallares-Ruiz, P Blanchet, M Mondain, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
September 10, 1975
[Primary liver cancer and hepatitis B infection in Senegal. Comparison of cancer patients with 2 control groups]
J Michon, A M Prince, W Szmuness, et al.
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Search research articles
Search
Showing results (81-90 of 112) with videos related to
Sort By:
Page
of 12
Molecular Human Reproduction
|
June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy
A Girardet, S Hamamah, H Déchaud, et al.
Molecular Human Reproduction
|
September 13, 2003
Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting
T Anahory, B Andréo, G Régnier-Vigouroux, et al.
Human Genetics
|
December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies
M Claustres, S Tuffery, M P Chevron, et al.
Human Mutation
|
January 1, 1994
A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patient
P Aguilar-Martinez, M C Romey, J C Gris, et al.
Human Genetics
|
September 1, 1994
Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applications
P Aguilar-Martinez, M C Romey, J F Schved, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies
C F Schmitt-Bernard, C Guittard, B Arnaud, et al.
Annals of Hematology
|
May 1, 1993
Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patient
P Aguilar-Martinez, F Galacteros, J F Schved, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Direct carrier detection for severe haemophilia A: application to families with no available affected male
C Maugard, P Aguilar-Martinez, J F Schved, et al.
Genetic Testing
|
April 19, 2002
Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness
N Pallares-Ruiz, P Blanchet, M Mondain, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
September 10, 1975
[Primary liver cancer and hepatitis B infection in Senegal. Comparison of cancer patients with 2 control groups]
J Michon, A M Prince, W Szmuness, et al.
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of 12