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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Clinical approach to the dysmorphic child]
V Cormier-Daire
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 26, 2004
[Genetics and the SHOX gene]
C Huber, V Cormier-Daire
American Journal of Medical Genetics
|
July 31, 2001
Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome
A Mégarbané, V Cormier-Daire
American Journal of Medical Genetics
|
March 14, 2002
Allelic and nonallelic heterogeneity in dyschondrosteosis (Leri-Weill syndrome)
V Cormier-Daire, C Huber, A Munnich
Clinical Genetics
|
March 4, 2014
Myhre syndrome
C Le Goff, C Michot, V Cormier-Daire
Journal of Medical Genetics
|
April 7, 2006
High incidence of SHOX anomalies in individuals with short stature
C Huber, M Rosilio, A Munnich, et al.
Clinical Genetics
|
August 25, 2004
New insights in congenital bowing of the femora
V Cormier-Daire, D Geneviève, A Munnich, et al.
Pediatric Radiology
|
August 10, 2000
Schmid type metaphyseal chondrodysplasia: a spondylometaphyseal dysplasia identical to the "Japanese" type
R Savarirayan, V Cormier-Daire, R S Lachman, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 28, 2008
[Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)]
G Baujat, A-S Lebre, V Cormier-Daire, et al.
American Journal of Medical Genetics
|
March 10, 2001
No evidence of unbalanced growth-related gene inheritance in a series of overgrowth syndrome patients
L Faivre, M Vekemans, D Sanlaville, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 144) with videos related to
Sort By:
Page
of 15
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Clinical approach to the dysmorphic child]
V Cormier-Daire
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 26, 2004
[Genetics and the SHOX gene]
C Huber, V Cormier-Daire
American Journal of Medical Genetics
|
July 31, 2001
Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome
A Mégarbané, V Cormier-Daire
American Journal of Medical Genetics
|
March 14, 2002
Allelic and nonallelic heterogeneity in dyschondrosteosis (Leri-Weill syndrome)
V Cormier-Daire, C Huber, A Munnich
Clinical Genetics
|
March 4, 2014
Myhre syndrome
C Le Goff, C Michot, V Cormier-Daire
Journal of Medical Genetics
|
April 7, 2006
High incidence of SHOX anomalies in individuals with short stature
C Huber, M Rosilio, A Munnich, et al.
Clinical Genetics
|
August 25, 2004
New insights in congenital bowing of the femora
V Cormier-Daire, D Geneviève, A Munnich, et al.
Pediatric Radiology
|
August 10, 2000
Schmid type metaphyseal chondrodysplasia: a spondylometaphyseal dysplasia identical to the "Japanese" type
R Savarirayan, V Cormier-Daire, R S Lachman, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 28, 2008
[Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)]
G Baujat, A-S Lebre, V Cormier-Daire, et al.
American Journal of Medical Genetics
|
March 10, 2001
No evidence of unbalanced growth-related gene inheritance in a series of overgrowth syndrome patients
L Faivre, M Vekemans, D Sanlaville, et al.
Page
of 15