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The Biochemical Journal|August 15, 1992
Intrinsic factor receptor during fetal development of the human intestineH Schohn, J L Guéant, B Leheup, et al.Molecular Genetics and Metabolism|September 21, 2013
Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?A Wiedemann, B Leheup, S-F Battaglia-Hsu, et al.American Journal of Medical Genetics. Part A|May 19, 2009
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardationC Bonnet, B Leheup, M Béri, et al.Journal of Human Genetics|July 25, 2008
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) geneC Bonnet, M-J Grégoire, M Vibert, et al.Neuroscience Letters|September 17, 2002
Unilateral trigeminal anaesthesia modifies postural control in human subjectsPierre Gangloff, Philippe P PerrinPresse Medicale (Paris, France : 1983)|October 28, 1995
[Early diagnosis and screening of cancer of the prostate]J P Fendler, P PerrinLa Revue Du Praticien|May 1, 1993
[Viewpoints of the urologist on acute pyelonephritis]J P Fendler, P PerrinThe International Journal of Developmental Biology|August 7, 1998
Differentiated aspect of female and male mouse mesonephroiM D Vazquez, P Bouchet, B Foliguet, et al.Anatomia, Histologia, Embryologia|November 18, 1998
3D reconstruction of the mouse's mesonephrosM D Vazquez, P Bouchet, J L Mallet, et al.Pediatric Dermatology|January 1, 1997
Eruptive familial lingual papillitis: a new entity?J P Lacour, C PerrinPageof 90