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L Faivre

Showing results (11-20 of 131) with videos related to

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American Journal of Medical Genetics|December 14, 1999
Can Hutchinson-Gilford progeria syndrome be a neonatal condition?L Faivre, P Khau Van Kien, N Madinier-Chappat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 7, 1999
[Prion diseases in pediatrics]I Sol-Caubel, F Castela, V Brousse, et al.
Bone Marrow Transplantation|July 11, 2017
Cord blood attached segment: is this a relevant quality control to predict a good hematopoietic stem cell graft?L Faivre, H Boucher, R Zerbib, et al.
Prenatal Diagnosis|July 5, 2001
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephalyC Thauvin-Robinet, T Rousseau, C Durand, et al.
American Journal of Medical Genetics|March 14, 2002
Septo-optic dysplasia and digital anomalies: another observationL Faivre, J Amiel, M Ouachée-Chardin, et al.
Clinical Dysmorphology|July 12, 2001
A novel syndrome with dwarfism, poorly muscled build, absent clavicles, humeroradial fusion, slender bones, oligodactyly and micrognathiaL Faivre, V Cormier-Daire, D Geneviève, et al.
Journal of Medical Genetics|February 12, 2002
Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome?J Amiel, L Faivre, L Wilson, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
Human Genetics|January 26, 2002
Mutation spectrum and splicing variants in the OPA1 geneC Delettre, J M Griffoin, J Kaplan, et al.
Pageof 14

Showing results (11-20 of 131) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics|December 14, 1999
Can Hutchinson-Gilford progeria syndrome be a neonatal condition?L Faivre, P Khau Van Kien, N Madinier-Chappat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 7, 1999
[Prion diseases in pediatrics]I Sol-Caubel, F Castela, V Brousse, et al.
Bone Marrow Transplantation|July 11, 2017
Cord blood attached segment: is this a relevant quality control to predict a good hematopoietic stem cell graft?L Faivre, H Boucher, R Zerbib, et al.
Prenatal Diagnosis|July 5, 2001
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephalyC Thauvin-Robinet, T Rousseau, C Durand, et al.
American Journal of Medical Genetics|March 14, 2002
Septo-optic dysplasia and digital anomalies: another observationL Faivre, J Amiel, M Ouachée-Chardin, et al.
Clinical Dysmorphology|July 12, 2001
A novel syndrome with dwarfism, poorly muscled build, absent clavicles, humeroradial fusion, slender bones, oligodactyly and micrognathiaL Faivre, V Cormier-Daire, D Geneviève, et al.
Journal of Medical Genetics|February 12, 2002
Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome?J Amiel, L Faivre, L Wilson, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
Human Genetics|January 26, 2002
Mutation spectrum and splicing variants in the OPA1 geneC Delettre, J M Griffoin, J Kaplan, et al.
Pageof 14