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M L Chauvet

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Pediatric Radiology|May 1, 1997
Osteochondrodysplasias, dysostoses, disorders of calcium metabolism, congenital malformations with skeletal involvement mapped on human chromosomesJ Frézal, M L Merrer, M L Chauvet
Journal De Genetique Humaine|June 1, 1988
[Marfan disease]M L Briard, M L Chauvet, J Kaplan
Journal De Genetique Humaine|May 1, 1987
[An unrecognized etiology of sexual ambiguity: Smith-Lemli-Opitz syndrome or a new entity?]M Le Merrer, M L Briard, M L Chauvet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Genetic diseases in mapping gene databases, genome interactive databases (GID)]A Munnich, M Le Merrer, M L Chauvet, et al.
Molecular Genetics and Metabolism|August 13, 1999
Human genes involved in chromatin remodeling in transcription initiation, and associated diseases: An overview using the GENATLAS databaseM Roux-Rouquie, M L Chauvet, A Munnich, et al.
Annales De Genetique|January 1, 1988
Genetic counselling, carrier detection, and prenatal diagnosis in hemophilia. A service experienceJ Kaplan, M L Chauvet, M L Briard, et al.
Annales De Pediatrie|January 1, 1991
[Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease]M le Merrer, M L Briard, M L Chauvet, et al.
Archives Francaises De Pediatrie|May 1, 1984
[Epidemiological and genetic study of 3 congenital cardiopathies with neonatal disclosure]M L Briard, M L Chauvet, M Le Merrer, et al.
Ophthalmic Genetics|March 1, 1995
Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritanceE Souied, P Amalric, M L Chauvet, et al.
Journal of Medical Genetics|July 7, 2000
Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardationV Cormier-Daire, M L Chauvet, S Lyonnet, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatric Radiology|May 1, 1997
Osteochondrodysplasias, dysostoses, disorders of calcium metabolism, congenital malformations with skeletal involvement mapped on human chromosomesJ Frézal, M L Merrer, M L Chauvet
Journal De Genetique Humaine|June 1, 1988
[Marfan disease]M L Briard, M L Chauvet, J Kaplan
Journal De Genetique Humaine|May 1, 1987
[An unrecognized etiology of sexual ambiguity: Smith-Lemli-Opitz syndrome or a new entity?]M Le Merrer, M L Briard, M L Chauvet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Genetic diseases in mapping gene databases, genome interactive databases (GID)]A Munnich, M Le Merrer, M L Chauvet, et al.
Molecular Genetics and Metabolism|August 13, 1999
Human genes involved in chromatin remodeling in transcription initiation, and associated diseases: An overview using the GENATLAS databaseM Roux-Rouquie, M L Chauvet, A Munnich, et al.
Annales De Genetique|January 1, 1988
Genetic counselling, carrier detection, and prenatal diagnosis in hemophilia. A service experienceJ Kaplan, M L Chauvet, M L Briard, et al.
Annales De Pediatrie|January 1, 1991
[Autosomal recessive metaphyseal chondrodysplasia and Hirschsprung's disease]M le Merrer, M L Briard, M L Chauvet, et al.
Archives Francaises De Pediatrie|May 1, 1984
[Epidemiological and genetic study of 3 congenital cardiopathies with neonatal disclosure]M L Briard, M L Chauvet, M Le Merrer, et al.
Ophthalmic Genetics|March 1, 1995
Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritanceE Souied, P Amalric, M L Chauvet, et al.
Journal of Medical Genetics|July 7, 2000
Genitopatellar syndrome: a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardationV Cormier-Daire, M L Chauvet, S Lyonnet, et al.
Pageof 2