Ouragini Houyem | Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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概要
- OURAGINI Houyemの詳細を見る
- 同名の論文著者
- Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Instituteの論文著者
関連著者
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Abdelhak Sonia
Molecular Investigation Of Genetic Orphan Diseases Institut Pasteur De Tunis
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Abdelhak Sonia
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (ur04/sp03) Institut Pasteur
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Ouragini Houyem
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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OURAGINI Houyem
"Molecular Investigation of Genetic Orphan Diseases" Research Unit (MIGOD), Institut Pasteur de Tuni
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CHERIF Faika
"Molecular Investigation of Genetic Orphan Diseases" Research Unit (MIGOD), Institut Pasteur de Tuni
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KASSAR Selma
Service d'Anatomo-Pathologie, Institut Pasteur de Tunis
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FLORIDDIA Giovanna
Laboratorio di Biologia Molecolare e Cellulare, Istituto Dermopatico dell'Immacolata-IRCCS
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PASCUCCI Monica
Laboratorio di Biologia Molecolare e Cellulare, Istituto Dermopatico dell'Immacolata-IRCCS
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DAOUD Wafa
Service de Dermatologie, Hopital La Rabta de Tunis
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OSMAN-DHAHRI Amel
Service de Dermatologie, Hopital La Rabta de Tunis
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BOUBAKER Samir
Service d'Anatomo-Pathologie, Institut Pasteur de Tunis
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CASTIGLIA Daniele
Laboratorio di Biologia Molecolare e Cellulare, Istituto Dermopatico dell'Immacolata-IRCCS
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ABDELHAK Sonia
"Molecular Investigation of Genetic Orphan Diseases" Research Unit (MIGOD), Institut Pasteur de Tuni
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Daoud Wafa
Service De Dermatologie Hopital La Rabta De Tunis
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Kassar Selma
Hereditary Keratinization Disorders" Research Unit Hopital La Rabta De Tunis
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Cherif Faika
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (migod) Institut Pasteur De T
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Boubaker Samir
Pathology Department Institut Pasteur De Tunis
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Ouragini Houyem
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (migod) Institut Pasteur De T
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Pascucci Monica
Laboratorio Di Biologia Molecolare E Cellulare Istituto Dermopatico Dell'immacolata-irccs
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Castiglia Daniele
Laboratorio Di Biologia Molecolare E Cellulare Istituto Dermopatico Dell'immacolata-irccs
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Osman Amel
Service De Dermatologie Hopital La Rabta De Tunis
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Floriddia Giovanna
Laboratorio Di Biologia Molecolare E Cellulare Istituto Dermopatico Dell'immacolata-irccs
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Kassar Selma
Service D'anatomo-pathologie Institut Pasteur De Tunis
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Boubaker Samir
Service D'anatomo-pathologie Institut Pasteur De Tunis
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Nouira Sonia
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur De Tunis
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Abdelhak Sonia
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (ur04/sp03) Institut Pasteur
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BRICK Sabrine
"Molecular Investigation of Genetic Orphan Diseases" Research Unit, Institut Pasteur de Tunis
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NOUIRA Sonia
"Molecular Investigation of Genetic Orphan Diseases" Research Unit, Institut Pasteur de Tunis
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KEFI Rym
"Molecular Investigation of Genetic Orphan Diseases" Research Unit, Institut Pasteur de Tunis
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MAHDHAOUI Nabiha
Service de Neonatologie, Hopital Farhat Hached
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MRAD Ridha
Service des maladies congenitales et hereditaires, Hopital Charles Nicolles
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RIDHA KAMOUN
Service de Dermatologie, Hopital Charles Nicolles
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DENGUEZLI Mohamed
Service de Dermatologie, Hopital Farhat Hached
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MONASTIRI Kamel
"Epidemiologie, Ethiopathogenie et Therapeutique des Malformations Congenitales en Tunisie" Research
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SEBOUI Hassen
Service de Neonatologie, Hopital Farhat Hached
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MOKNI Mourad
Service de Dermatologie, Hopital La Rabta de Tunis
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Brick Sabrine
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur De Tunis
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Ridha Kamoun
Service De Dermatologie Hopital Charles Nicolles
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Mrad Ridha
Service Des Maladies Congenitales Et Hereditaires Hopital Charles Nicolles
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Kefi Rym
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur De Tunis
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Mokni Mourad
Service De Dermatologie Hopital La Rabta De Tunis
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Seboui Hassen
Service De Neonatologie Hopital Farhat Hached
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Monastiri Kamel
Epidemiologie Ethiopathogenie Et Therapeutique Des Malformations Congenitales En Tunisie" Resea
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Mahdhaoui Nabiha
Service De Neonatologie Hopital Farhat Hached
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Denguezli Mohamed
Service De Dermatologie Hopital Farhat Hached
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Munier Francis
Unit Of Oculogenomics Institute For Research In Ophthalmology
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Rebai Ahmed
Department Of Bioinformatics Center Of Biotechnology Of Sfax
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Nouira Sonia
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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OUECHTATI Farah
Molecular Investigation of Genetic Orphan Diseases Research Unit UR04/SP03, Pasteur Institute
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MERDASSI Ahlem
Oculogenetics Research Unit 17/04, Hedi Rais Institute of Ophthalmology
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BOUYACOUB Yosra
Molecular Investigation of Genetic Orphan Diseases Research Unit UR04/SP03, Pasteur Institute
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LARGUECHE Leila
Oculogenetics Research Unit 17/04, Hedi Rais Institute of Ophthalmology
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DEROUICHE Kaouther
Oculogenetics Research Unit 17/04, Hedi Rais Institute of Ophthalmology
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TIAB Leila
Unit of Oculogenomics, Institute for Research in Ophthalmology
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BAKLOUTI Karim
Oculogenetics Research Unit 17/04, Hedi Rais Institute of Ophthalmology
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SCHORDERET Daniel
Unit of Oculogenomics, Institute for Research in Ophthalmology
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ZOGRAFOS Leonidas
Swiss Federal Institute of Technology, University of Lausanne
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MATRI Leila
Oculogenetics Research Unit 17/04, Hedi Rais Institute of Ophthalmology
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Tiab Leila
Unit Of Oculogenomics Institute For Research In Ophthalmology
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Matri Leila
Oculogenetics Research Unit 17/04 Hedi Rais Institute Of Ophthalmology
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Baklouti Karim
Oculogenetics Research Unit 17/04 Hedi Rais Institute Of Ophthalmology
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Largueche Leila
Oculogenetics Research Unit 17/04 Hedi Rais Institute Of Ophthalmology
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Ouechtati Farah
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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Zografos Leonidas
Swiss Federal Institute Of Technology University Of Lausanne
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Derouiche Kaouther
Oculogenetics Research Unit 17/04 Hedi Rais Institute Of Ophthalmology
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Schorderet Daniel
Unit Of Oculogenomics Institute For Research In Ophthalmology
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Bouyacoub Yosra
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
著作論文
- Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family
- Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
- Clinical and genetic investigation of a large Tunisian family with complete achromatopsia : identification of a new nonsense mutation in GNAT2 gene