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M Clementi
C Stoll

Showing results (41-50 of 650) with videos related to

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Pathologica|November 1, 1986
[Registry of congenital malformation. Performing the follow-up]R Tenconi, M Clementi
Advances in Biochemical Engineering/Biotechnology|January 1, 1987
Serum-free growth of human hepatoma cells. A reviewP Bagnarelli, M Clementi
Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C Stoll
Annales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P Sauvage
Annales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D Eyer
Annales De Pediatrie|January 1, 1979
[Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18]C Stoll, J Messer
Clinical Genetics|November 27, 1998
Autosomal dominant carpal tunnel syndromeC Stoll, D Maitrot
Lancet (London, England)|December 21, 1996
Routine fetal echocardiography and detection of congenital heart diseaseY Alembik, C Stoll
Der Internist|December 25, 2010
[Complementary therapy in palliative medicine]J Hübner, C Stoll
Annales De Genetique|January 9, 1999
A patient with 13q-syndrome with mild mental retardation and with growth retardationC Stoll, Y Alembik
Pageof 65

Showing results (41-50 of 650) with videos related to

Sort By:
Pageof 65
Pathologica|November 1, 1986
[Registry of congenital malformation. Performing the follow-up]R Tenconi, M Clementi
Advances in Biochemical Engineering/Biotechnology|January 1, 1987
Serum-free growth of human hepatoma cells. A reviewP Bagnarelli, M Clementi
Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C Stoll
Annales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P Sauvage
Annales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D Eyer
Annales De Pediatrie|January 1, 1979
[Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18]C Stoll, J Messer
Clinical Genetics|November 27, 1998
Autosomal dominant carpal tunnel syndromeC Stoll, D Maitrot
Lancet (London, England)|December 21, 1996
Routine fetal echocardiography and detection of congenital heart diseaseY Alembik, C Stoll
Der Internist|December 25, 2010
[Complementary therapy in palliative medicine]J Hübner, C Stoll
Annales De Genetique|January 9, 1999
A patient with 13q-syndrome with mild mental retardation and with growth retardationC Stoll, Y Alembik
Pageof 65