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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.Pageof 37