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A Munnich

Showing results (271-280 of 426) with videos related to

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American Journal of Human Genetics|February 1, 1995
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13S Gerber, J M Rozet, D Bonneau, et al.
Nature Genetics|March 1, 1994
A gene for achondroplasia-hypochondroplasia maps to chromosome 4pM Le Merrer, F Rousseau, L Legeai-Mallet, et al.
Human Molecular Genetics|May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19pM Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
American Journal of Human Genetics|July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiencyJ C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
British Journal of Haematology|June 1, 1994
Refractory anaemia and mitochondrial cytopathy in childhoodB Bader-Meunier, A Rötig, F Mielot, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
American Journal of Human Genetics|April 1, 1991
Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5P Sheth, S Abdelhak, M F Bachelot, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
[Mutations of RET proto-oncogene in Hirschsprung disease]S Lyonnet, P Edery, L M Mulligan, et al.
Nature|January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's diseaseP Edery, S Lyonnet, L M Mulligan, et al.
Pageof 43

Showing results (271-280 of 426) with videos related to

Sort By:
Pageof 43
American Journal of Human Genetics|February 1, 1995
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13S Gerber, J M Rozet, D Bonneau, et al.
Nature Genetics|March 1, 1994
A gene for achondroplasia-hypochondroplasia maps to chromosome 4pM Le Merrer, F Rousseau, L Legeai-Mallet, et al.
Human Molecular Genetics|May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19pM Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
American Journal of Human Genetics|July 31, 1998
A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiencyJ C von Kleist-Retzow, V Cormier-Daire, P de Lonlay, et al.
British Journal of Haematology|June 1, 1994
Refractory anaemia and mitochondrial cytopathy in childhoodB Bader-Meunier, A Rötig, F Mielot, et al.
Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.
American Journal of Human Genetics|April 1, 1991
Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5P Sheth, S Abdelhak, M F Bachelot, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
[Mutations of RET proto-oncogene in Hirschsprung disease]S Lyonnet, P Edery, L M Mulligan, et al.
Nature|January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's diseaseP Edery, S Lyonnet, L M Mulligan, et al.
Pageof 43