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Human Genetics
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May 31, 2001
Segregation of a mutation in CNGB1 encoding the beta-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa
C Bareil, C P Hamel, V Delague, et al.
Trends in Microbiology
|
July 7, 2009
Gene Ontology and the annotation of pathogen genomes: the case of Candida albicans
Martha B Arnaud, Maria C Costanzo, Prachi Shah, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
European Journal of Applied Physiology
|
May 3, 2005
Ulnar and tibial bending stiffness as an index of bone strength in synchronized swimmers and gymnasts
Michael T C Liang, Sara B Arnaud, Charles R Steele, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Nouvelle Revue Francaise D'Hematologie
|
April 14, 1978
[Ocular localization appearing in a child with acute lymphoblastosis after hematological remission for 18 months]
D Dossa, B Arnaud, M Weil, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene
F Marlhens, J M Griffoin, C Bareil, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1994
[Trans-scleral cyclo-photocoagulation. Results over 6 months]
I Aubry, B Arnaud, C Reda, et al.
Experimental Eye Research
|
January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutations
L Beaufrère, S Tuffery, C Hamel, et al.
Laboratory Animal Science
|
December 1, 1994
Metabolic cages for a space flight model in the rat
J S Harper, G M Mulenburg, J Evans, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 207) with videos related to
Sort By:
Page
of 21
Human Genetics
|
May 31, 2001
Segregation of a mutation in CNGB1 encoding the beta-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa
C Bareil, C P Hamel, V Delague, et al.
Trends in Microbiology
|
July 7, 2009
Gene Ontology and the annotation of pathogen genomes: the case of Candida albicans
Martha B Arnaud, Maria C Costanzo, Prachi Shah, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
European Journal of Applied Physiology
|
May 3, 2005
Ulnar and tibial bending stiffness as an index of bone strength in synchronized swimmers and gymnasts
Michael T C Liang, Sara B Arnaud, Charles R Steele, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Nouvelle Revue Francaise D'Hematologie
|
April 14, 1978
[Ocular localization appearing in a child with acute lymphoblastosis after hematological remission for 18 months]
D Dossa, B Arnaud, M Weil, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene
F Marlhens, J M Griffoin, C Bareil, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1994
[Trans-scleral cyclo-photocoagulation. Results over 6 months]
I Aubry, B Arnaud, C Reda, et al.
Experimental Eye Research
|
January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutations
L Beaufrère, S Tuffery, C Hamel, et al.
Laboratory Animal Science
|
December 1, 1994
Metabolic cages for a space flight model in the rat
J S Harper, G M Mulenburg, J Evans, et al.
Page
of 21