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C Piussan

Showing results (91-100 of 112) with videos related to

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Chirurgie Pediatrique|January 1, 1985
[A new case of non-secreting adrenocortical tumor in a child]J P Canarelli, J C Pautard, B Pautard, et al.
American Journal of Human Genetics|January 1, 1995
X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21C Piussan, A Hanauer, N Dahl, et al.
Annales De Pediatrie|September 1, 1989
[Diverticulum of the stomach in children. Apropos of a case of congenital diverticulum]P H Benhamou, C Lenaerts, J P Canarelli, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
Nephrologie|January 1, 1987
[Evaluation of maximal filtration capacity and renal functional reserve by an oral protein-loading test in adults and children]M F Colome, B Boudailliez, H Renaud, et al.
American Journal of Human Genetics|April 1, 1995
Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26N Dahl, J Laporte, L Hu, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 1997
Possible person-to-person transmission of Escherichia coli O111--associated hemolytic uremic syndromeB Boudailliez, P Berquin, P Mariani-Kurkdjian, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.
Presse Medicale (Paris, France : 1983)|June 17, 1989
[African trypanosomiasis in children treated with eflornithine. A case]P H Benhamou, J Chandenier, P J Schechter, et al.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Chirurgie Pediatrique|January 1, 1985
[A new case of non-secreting adrenocortical tumor in a child]J P Canarelli, J C Pautard, B Pautard, et al.
American Journal of Human Genetics|January 1, 1995
X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21C Piussan, A Hanauer, N Dahl, et al.
Annales De Pediatrie|September 1, 1989
[Diverticulum of the stomach in children. Apropos of a case of congenital diverticulum]P H Benhamou, C Lenaerts, J P Canarelli, et al.
American Journal of Medical Genetics|January 30, 1995
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?P Saugier-Veber, A Munnich, S Lyonnet, et al.
Nephrologie|January 1, 1987
[Evaluation of maximal filtration capacity and renal functional reserve by an oral protein-loading test in adults and children]M F Colome, B Boudailliez, H Renaud, et al.
American Journal of Human Genetics|April 1, 1995
Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26N Dahl, J Laporte, L Hu, et al.
Pediatric Nephrology (Berlin, Germany)|February 1, 1997
Possible person-to-person transmission of Escherichia coli O111--associated hemolytic uremic syndromeB Boudailliez, P Berquin, P Mariani-Kurkdjian, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.
Presse Medicale (Paris, France : 1983)|June 17, 1989
[African trypanosomiasis in children treated with eflornithine. A case]P H Benhamou, J Chandenier, P J Schechter, et al.
Pageof 12