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M Le Merrer

Showing results (51-60 of 188) with videos related to

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Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
Journal De Genetique Humaine|September 1, 1980
[Pregnancy abnormalities as alerting signs of Steinert's congenital myotonic dystrophy]M L Briard, M Le Merrer, F Goutieres, et al.
American Journal of Medical Genetics|March 29, 1996
Genetic study of scaphocephalyE Lajeunie, M Le Merrer, C Bonaïti-Pellie, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Long-term follow-up in a patient with metatropic dysplasiaD Geneviève, M Le Merrer, A Munnich, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 30, 2005
[Ghosal haematodiaphyseal dysplasia: a new case]C Vignon-Savoye, M Le Merrer, A Vincens, et al.
American Journal of Medical Genetics|February 13, 1995
Genetic study of nonsyndromic coronal craniosynostosisE Lajeunie, M Le Merrer, C Bonaïti-Pellie, et al.
Journal De Genetique Humaine|August 1, 1988
[Genetic counseling in craniostenosis. Results of a prospective study performed with a group of studies on craniofacial malformations]M Le Merrer, V Ledinot, D Renier, et al.
Archives Francaises De Pediatrie|October 1, 1980
[Epidemiologic and genetic studies of spina bifida (author's transl)]M Le Merrer, M L Briard, F Demenais, et al.
Journal of Neurosurgery|April 13, 2000
Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcomeD Renier, V El-Ghouzzi, J Bonaventure, et al.
European Journal of Pediatrics|May 1, 1995
Acral dysostosis dyserythropoiesis syndromeM Le Merrer, R Girot, P Parent, et al.
Pageof 19

Showing results (51-60 of 188) with videos related to

Sort By:
Pageof 19
Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
Journal De Genetique Humaine|September 1, 1980
[Pregnancy abnormalities as alerting signs of Steinert's congenital myotonic dystrophy]M L Briard, M Le Merrer, F Goutieres, et al.
American Journal of Medical Genetics|March 29, 1996
Genetic study of scaphocephalyE Lajeunie, M Le Merrer, C Bonaïti-Pellie, et al.
American Journal of Medical Genetics. Part A|May 13, 2005
Long-term follow-up in a patient with metatropic dysplasiaD Geneviève, M Le Merrer, A Munnich, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 30, 2005
[Ghosal haematodiaphyseal dysplasia: a new case]C Vignon-Savoye, M Le Merrer, A Vincens, et al.
American Journal of Medical Genetics|February 13, 1995
Genetic study of nonsyndromic coronal craniosynostosisE Lajeunie, M Le Merrer, C Bonaïti-Pellie, et al.
Journal De Genetique Humaine|August 1, 1988
[Genetic counseling in craniostenosis. Results of a prospective study performed with a group of studies on craniofacial malformations]M Le Merrer, V Ledinot, D Renier, et al.
Archives Francaises De Pediatrie|October 1, 1980
[Epidemiologic and genetic studies of spina bifida (author's transl)]M Le Merrer, M L Briard, F Demenais, et al.
Journal of Neurosurgery|April 13, 2000
Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcomeD Renier, V El-Ghouzzi, J Bonaventure, et al.
European Journal of Pediatrics|May 1, 1995
Acral dysostosis dyserythropoiesis syndromeM Le Merrer, R Girot, P Parent, et al.
Pageof 19