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S Lyonnet

Showing results (51-60 of 223) with videos related to

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Lancet (London, England)|September 16, 1989
Localisation of focal lesion permitting partial pancreatectomy in infantsS Lyonnet, J P Bonnefont, J M Saudubray, et al.
The New England Journal of Medicine|August 12, 2000
Familial forms of thyroid dysgenesis among infants with congenital hypothyroidismM Castanet, S Lyonnet, C Bonaïti-Pellié, et al.
Heart (British Cardiac Society)|August 24, 2000
Mechanical properties of the common carotid artery in Williams syndromeY Aggoun, D Sidi, B I Levy, et al.
Journal of Medical Genetics|May 5, 1999
Tricuspid atresia and conotruncal malformations in five familiesD Bonnet, L Fermont, J Kachaner, et al.
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
Journal of Medical Genetics|January 1, 1992
Blepharophimosis, eczema, and growth and developmental delay in a young adult: late features of Dubowitz syndrome?S Lyonnet, G Schwartz, G Gatin, et al.
Annales De Dermatologie Et De Venereologie|November 7, 1998
[Angiomatous and cerulodermic macules: early cutaneous signs of neurofibromatosis type I]P Vabres, P de Lonlay, J Amiel, et al.
Journal of Medical Genetics|January 1, 1991
Two distinct mutations at a single BamHI site in phenylketonuriaD Melle, P Verelst, F Rey, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Pageof 23

Showing results (51-60 of 223) with videos related to

Sort By:
Pageof 23
Lancet (London, England)|September 16, 1989
Localisation of focal lesion permitting partial pancreatectomy in infantsS Lyonnet, J P Bonnefont, J M Saudubray, et al.
The New England Journal of Medicine|August 12, 2000
Familial forms of thyroid dysgenesis among infants with congenital hypothyroidismM Castanet, S Lyonnet, C Bonaïti-Pellié, et al.
Heart (British Cardiac Society)|August 24, 2000
Mechanical properties of the common carotid artery in Williams syndromeY Aggoun, D Sidi, B I Levy, et al.
Journal of Medical Genetics|May 5, 1999
Tricuspid atresia and conotruncal malformations in five familiesD Bonnet, L Fermont, J Kachaner, et al.
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
Journal of Medical Genetics|January 1, 1992
Blepharophimosis, eczema, and growth and developmental delay in a young adult: late features of Dubowitz syndrome?S Lyonnet, G Schwartz, G Gatin, et al.
Annales De Dermatologie Et De Venereologie|November 7, 1998
[Angiomatous and cerulodermic macules: early cutaneous signs of neurofibromatosis type I]P Vabres, P de Lonlay, J Amiel, et al.
Journal of Medical Genetics|January 1, 1991
Two distinct mutations at a single BamHI site in phenylketonuriaD Melle, P Verelst, F Rey, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Pageof 23