L Bachner|J C Kaplan - JoVE Visualize

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The European Respiratory Journal|November 1, 1996

Genotype-phenotype relationships in a cohort of adult cystic fibrosis patientsD Hubert, T Bienvenu, N Desmazes-Dufeu, et al.

The European Respiratory Journal|August 13, 1999

Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritisX Puéchal, I Fajac, T Bienvenu, et al.

British Journal of Haematology|April 1, 1990

Ras activation in myelodysplastic syndromes: clinical and molecular study of the chronic phase of the diseaseC Melani, A Haliassos, J C Chomel, et al.

Croatian Medical Journal|November 7, 2000

Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophyN Canki-Klain, D Récan, D Milicić, et al.

Human Genetics|November 1, 1994

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in AlgeriaK Nafa, A Reghis, N Osmani, et al.

The European Respiratory Journal|January 7, 1999

Relationships between nasal potential difference and respiratory function in adults with cystic fibrosisI Fajac, D Hubert, T Bienvenu, et al.

Antimicrobial Agents and Chemotherapy|February 1, 1994

Resistance to 2',3'-dideoxycytidine conferred by a mutation in codon 65 of the human immunodeficiency virus type 1 reverse transcriptaseD Zhang, A M Caliendo, J J Eron, et al.

Annales De Medecine Interne|January 1, 1986

[Prenatal diagnosis of hemophilia A by analysis of DNA]M Delpech, P Maisonneuve, M Baudis, et al.

American Journal of Medical Genetics|July 12, 1996

X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pterV des Portes, L Bachner, T Brüls, et al.

Human Genetics|April 1, 1990

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in AlgeriaK Nafa, F Meriane, A Reghis, et al.

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Showing results (131-140 of 185) with videos related to

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Pageof 19

The European Respiratory Journal|November 1, 1996

Genotype-phenotype relationships in a cohort of adult cystic fibrosis patientsD Hubert, T Bienvenu, N Desmazes-Dufeu, et al.

The European Respiratory Journal|August 13, 1999

Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritisX Puéchal, I Fajac, T Bienvenu, et al.

British Journal of Haematology|April 1, 1990

Ras activation in myelodysplastic syndromes: clinical and molecular study of the chronic phase of the diseaseC Melani, A Haliassos, J C Chomel, et al.

Croatian Medical Journal|November 7, 2000

Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophyN Canki-Klain, D Récan, D Milicić, et al.

Human Genetics|November 1, 1994

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in AlgeriaK Nafa, A Reghis, N Osmani, et al.

The European Respiratory Journal|January 7, 1999

Relationships between nasal potential difference and respiratory function in adults with cystic fibrosisI Fajac, D Hubert, T Bienvenu, et al.

Antimicrobial Agents and Chemotherapy|February 1, 1994

Resistance to 2',3'-dideoxycytidine conferred by a mutation in codon 65 of the human immunodeficiency virus type 1 reverse transcriptaseD Zhang, A M Caliendo, J J Eron, et al.

Annales De Medecine Interne|January 1, 1986

[Prenatal diagnosis of hemophilia A by analysis of DNA]M Delpech, P Maisonneuve, M Baudis, et al.

American Journal of Medical Genetics|July 12, 1996

X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pterV des Portes, L Bachner, T Brüls, et al.

Human Genetics|April 1, 1990

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in AlgeriaK Nafa, F Meriane, A Reghis, et al.

Pageof 19