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S Rossignol

Showing results (111-120 of 116) with videos related to

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Progress in Brain Research|November 21, 2002
The cat model of spinal injuryS Rossignol, C Chau, N Giroux, et al.
Hormone Research in Paediatrics|December 17, 2013
Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillanceF Brioude, A Lacoste, I Netchine, et al.
Journal of Medical Genetics|September 26, 2013
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndromeF Brioude, I Oliver-Petit, A Blaise, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 4, 2014
Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumorsF Bertoin, E Letouzé, P Grignani, et al.
Pediatric Blood & Cancer|August 24, 2013
Malformations, genetic abnormalities, and Wilms tumorS Dumoucel, M Gauthier-Villars, D Stoppa-Lyonnet, et al.
Clinical Genetics|October 6, 2012
OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairmentC Thauvin-Robinet, S Thomas, M Sinico, et al.
Pageof 12

Showing results (111-120 of 116) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 116 results.
Progress in Brain Research|November 21, 2002
The cat model of spinal injuryS Rossignol, C Chau, N Giroux, et al.
Hormone Research in Paediatrics|December 17, 2013
Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillanceF Brioude, A Lacoste, I Netchine, et al.
Journal of Medical Genetics|September 26, 2013
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndromeF Brioude, I Oliver-Petit, A Blaise, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 4, 2014
Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumorsF Bertoin, E Letouzé, P Grignani, et al.
Pediatric Blood & Cancer|August 24, 2013
Malformations, genetic abnormalities, and Wilms tumorS Dumoucel, M Gauthier-Villars, D Stoppa-Lyonnet, et al.
Clinical Genetics|October 6, 2012
OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairmentC Thauvin-Robinet, S Thomas, M Sinico, et al.
Pageof 12