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P Edery

Showing results (1-10 of 54) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 26, 2004
[From morphological features to diagnostics of unexplained mental retardation: a new clinical classification?]P Edery
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|May 1, 1997
RET in human development and oncogenesisP Edery, C Eng, A Munnich, et al.
Pathologie-Biologie|May 10, 2008
[New chromosomal syndromes]C Schluth-Bolard, M Till, P Edery, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|August 1, 1996
Waardenburg-Hirschsprung disease in two sisters: a possible clue to the genetics of this association?J P Bonnet, M Till, P Edery, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Identification of mutation of RET proto-oncogene in Hirschsprung disease]T Attié, P Edery, S Lyonnet, et al.
Clinical Genetics|March 1, 2005
Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardationG Lesca, Om Sinilnikova, G Theuil, et al.
Neuropediatrics|June 21, 2001
Mitochondrial respiratory chain deficiency revealed by hypothermiaF Cholley, P Edery, D Ricquier, et al.
Neuro-Chirurgie|October 13, 2019
Genetic bases of craniosynostoses: An updateT Armand, E Schaefer, F Di Rocco, et al.
Journal Francais D'Ophtalmologie|July 5, 2003
[The genetics of hereditary cataract]F Beby, L Morle, L Michon, et al.
Annales De Genetique|May 20, 2000
Cerebellar ataxia and mental retardation in a child with an inherited satellited chromosome 4qL Faivre, I Radford, G Viot, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 26, 2004
[From morphological features to diagnostics of unexplained mental retardation: a new clinical classification?]P Edery
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|May 1, 1997
RET in human development and oncogenesisP Edery, C Eng, A Munnich, et al.
Pathologie-Biologie|May 10, 2008
[New chromosomal syndromes]C Schluth-Bolard, M Till, P Edery, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|August 1, 1996
Waardenburg-Hirschsprung disease in two sisters: a possible clue to the genetics of this association?J P Bonnet, M Till, P Edery, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Identification of mutation of RET proto-oncogene in Hirschsprung disease]T Attié, P Edery, S Lyonnet, et al.
Clinical Genetics|March 1, 2005
Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardationG Lesca, Om Sinilnikova, G Theuil, et al.
Neuropediatrics|June 21, 2001
Mitochondrial respiratory chain deficiency revealed by hypothermiaF Cholley, P Edery, D Ricquier, et al.
Neuro-Chirurgie|October 13, 2019
Genetic bases of craniosynostoses: An updateT Armand, E Schaefer, F Di Rocco, et al.
Journal Francais D'Ophtalmologie|July 5, 2003
[The genetics of hereditary cataract]F Beby, L Morle, L Michon, et al.
Annales De Genetique|May 20, 2000
Cerebellar ataxia and mental retardation in a child with an inherited satellited chromosome 4qL Faivre, I Radford, G Viot, et al.
Pageof 6