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P Guibaud

Showing results (131-140 of 147) with videos related to

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Journal De Genetique Humaine|September 1, 1985
[Fetal ascites as a manifestation of infantile sialidosis. Significance of a study of oligosaccharides in amniotic fluid]P Guibaud, X Cottin, I Maire, et al.
Annales De Genetique|March 1, 1978
[7 cases of trisomy 2q34 leads to 2qter resulting from a familial t(2;8)(q34;23)]C Laurent, M C Biemont, P Guibaud, et al.
European Journal of Pediatrics|April 1, 1986
Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus materialE A Kvittingen, P P Guibaud, P Divry, et al.
Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.
Journal De Genetique Humaine|February 1, 1981
[Acetylcholinesterase: an additional test for diagnosis of fetal malformations]S Guibaud, A Simplot, M Bonnet, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Human Mutation|January 1, 1992
A splice junction mutation in intron 2 of the carbonic anhydrase II gene of osteopetrosis patients from Arabic countriesP Y Hu, D E Roth, L A Skaggs, et al.
Pediatrie|December 1, 1984
[Cysteamine in the treatment of cystinosis in children. In vitro and in vivo studies]J J Louis, P Guibaud, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Primapterinuria: a new variant of atypical phenylketonuriaN Blau, H C Curtius, T Kuster, et al.
Journal De Genetique Humaine|August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]H Plauchu, M P Cordier, H N Carrier, et al.
Pageof 15

Showing results (131-140 of 147) with videos related to

Sort By:
Pageof 15
Journal De Genetique Humaine|September 1, 1985
[Fetal ascites as a manifestation of infantile sialidosis. Significance of a study of oligosaccharides in amniotic fluid]P Guibaud, X Cottin, I Maire, et al.
Annales De Genetique|March 1, 1978
[7 cases of trisomy 2q34 leads to 2qter resulting from a familial t(2;8)(q34;23)]C Laurent, M C Biemont, P Guibaud, et al.
European Journal of Pediatrics|April 1, 1986
Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus materialE A Kvittingen, P P Guibaud, P Divry, et al.
Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.
Journal De Genetique Humaine|February 1, 1981
[Acetylcholinesterase: an additional test for diagnosis of fetal malformations]S Guibaud, A Simplot, M Bonnet, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Human Mutation|January 1, 1992
A splice junction mutation in intron 2 of the carbonic anhydrase II gene of osteopetrosis patients from Arabic countriesP Y Hu, D E Roth, L A Skaggs, et al.
Pediatrie|December 1, 1984
[Cysteamine in the treatment of cystinosis in children. In vitro and in vivo studies]J J Louis, P Guibaud, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Primapterinuria: a new variant of atypical phenylketonuriaN Blau, H C Curtius, T Kuster, et al.
Journal De Genetique Humaine|August 1, 1987
[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)]H Plauchu, M P Cordier, H N Carrier, et al.
Pageof 15