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Annales D'Immunologie
|
May 1, 1983
[Polyacrylamide-induced subcutaneous inflammation in mice]
F Hérodin, P Calvas, D Dormont, et al.
Bulletin De L'Association Des Anatomistes
|
December 1, 1987
[Chromosome anomalies and male infertility. A study of 1,444 subjects]
G Bourrouillou, A Mansat, P Calvas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 4, 1999
Expression of a liver/bone-intestinal hybrid of alkaline phosphatase in neutrophils of Down's syndrome patients
H Vergnes, J Grozdea, C Denier, et al.
Human Mutation
|
January 26, 2006
Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia
N Chassaing, S Bourthoumieu, M Cossee, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
August 1, 1994
Length polymorphism of a microsatellite in human and non human primates
P Calvas, A Blancher, I Salvignol, et al.
Acta Haematologica
|
March 22, 2000
Neutrophil alkaline phosphatase activity in Turner syndrome
J Grozdea, H Vergnes, J P Cambus, et al.
Journal of Medical Genetics
|
May 17, 2005
Pseudoxanthoma elasticum: a clinical, pathophysiological and genetic update including 11 novel ABCC6 mutations
N Chassaing, L Martin, P Calvas, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia
M C Vincent, V Biancalana, D Ginisty, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 21, 2018
Prenatal diagnosis of Norrie disease based on ultrasound findings
C Dubucs, M Merveille, S Kessler, et al.
Annales De Genetique
|
October 20, 1999
Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity
L Naiglin, J Clayton, C Gazagne, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Annales D'Immunologie
|
May 1, 1983
[Polyacrylamide-induced subcutaneous inflammation in mice]
F Hérodin, P Calvas, D Dormont, et al.
Bulletin De L'Association Des Anatomistes
|
December 1, 1987
[Chromosome anomalies and male infertility. A study of 1,444 subjects]
G Bourrouillou, A Mansat, P Calvas, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 4, 1999
Expression of a liver/bone-intestinal hybrid of alkaline phosphatase in neutrophils of Down's syndrome patients
H Vergnes, J Grozdea, C Denier, et al.
Human Mutation
|
January 26, 2006
Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia
N Chassaing, S Bourthoumieu, M Cossee, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
August 1, 1994
Length polymorphism of a microsatellite in human and non human primates
P Calvas, A Blancher, I Salvignol, et al.
Acta Haematologica
|
March 22, 2000
Neutrophil alkaline phosphatase activity in Turner syndrome
J Grozdea, H Vergnes, J P Cambus, et al.
Journal of Medical Genetics
|
May 17, 2005
Pseudoxanthoma elasticum: a clinical, pathophysiological and genetic update including 11 novel ABCC6 mutations
N Chassaing, L Martin, P Calvas, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia
M C Vincent, V Biancalana, D Ginisty, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 21, 2018
Prenatal diagnosis of Norrie disease based on ultrasound findings
C Dubucs, M Merveille, S Kessler, et al.
Annales De Genetique
|
October 20, 1999
Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity
L Naiglin, J Clayton, C Gazagne, et al.
Page
of 8