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C Dorche

Showing results (41-50 of 48) with videos related to

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American Journal of Obstetrics and Gynecology|October 1, 1990
Antenatal diagnosis of molybdenum cofactor deficiencyR G Gray, A Green, S N Basu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1994
[Sulfite oxidase deficiency presenting as Leigh syndrome]J Amiel, V Gagey, D Rabier, 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.
Annales De Biologie Clinique|January 1, 1977
["Enzymology" commission. Current enzymology in clinical chemistry and recommendations for the measurement of catalytic activities in the serum at 30 degrees C]M Mathieu, J P Bretaudiere, M M Galteau, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markersA Shalata, H Mandel, C Dorche, et al.
Pediatrics|June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Y Pang, M A Wallace, L Hofman, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a gene for molybdenum cofactor deficiency, on the short arm of chromosome 6, by homozygosity mappingA Shalata, H Mandel, J Reiss, et al.
Bone Marrow Transplantation|June 11, 2003
Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sourcesG Souillet, N Guffon, I Maire, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
American Journal of Obstetrics and Gynecology|October 1, 1990
Antenatal diagnosis of molybdenum cofactor deficiencyR G Gray, A Green, S N Basu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1994
[Sulfite oxidase deficiency presenting as Leigh syndrome]J Amiel, V Gagey, D Rabier, 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.
Annales De Biologie Clinique|January 1, 1977
["Enzymology" commission. Current enzymology in clinical chemistry and recommendations for the measurement of catalytic activities in the serum at 30 degrees C]M Mathieu, J P Bretaudiere, M M Galteau, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markersA Shalata, H Mandel, C Dorche, et al.
Pediatrics|June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Y Pang, M A Wallace, L Hofman, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a gene for molybdenum cofactor deficiency, on the short arm of chromosome 6, by homozygosity mappingA Shalata, H Mandel, J Reiss, et al.
Bone Marrow Transplantation|June 11, 2003
Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sourcesG Souillet, N Guffon, I Maire, et al.
Pageof 5