Mokni Mourad | Service De Dermatologie Hopital La Rabta De Tunis
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概要
関連著者
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Kassar Selma
Hereditary Keratinization Disorders" Research Unit Hopital La Rabta De Tunis
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Abdelhak Sonia
Molecular Investigation Of Genetic Orphan Diseases Institut Pasteur De Tunis
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Boubaker Samir
Pathology Department 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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Mokni Mourad
Service De Dermatologie Hopital La Rabta De Tunis
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Abdelhak Sonia
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (ur04/sp03) Institut Pasteur
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BOUBAKER Samir
Service d'Anatomo-Pathologie, Institut Pasteur de Tunis
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ABDELHAK Sonia
"Molecular Investigation of Genetic Orphan Diseases" Research Unit (MIGOD), Institut Pasteur de Tuni
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Osman Amel
Service De Dermatologie Hopital La Rabta De Tunis
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MOKNI Mourad
Service de Dermatologie, Hopital La Rabta de Tunis
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REBAI Ahmed
Bioinformatic department, Centre de Biotechnologie de Sfax
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Rebai Ahmed
Bioinformatic Department Centre De Biotechnologie De Sfax
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Boubaker Samir
Service D'anatomo-pathologie Institut Pasteur De Tunis
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Charfeddine Cherine
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur De Tunis
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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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CASTIGLIA Daniele
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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Cherif Faika
Molecular Investigation Of Genetic Orphan Diseases" Research Unit (migod) Institut Pasteur De T
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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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Floriddia Giovanna
Laboratorio Di Biologia Molecolare E Cellulare Istituto Dermopatico Dell'immacolata-irccs
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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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BCHETNIA Mbarka
"Molecular Investigation of Genetic Orphan Diseases" Research Unit, Institut Pasteur de Tunis
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CHARFEDDINE Cherine
"Molecular Investigation of Genetic Orphan Diseases" Research Unit, Institut Pasteur de Tunis
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KASSAR Selma
"Hereditary Keratinization Disorders" Research Unit, Hopital La Rabta de Tunis
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HANCHI Imen
Dermatology Department, Hopital La Rabta
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TOUNSI-GUETTITI Haifa
Pathology Department, Institut Pasteur de Tunis
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DHAHRI-BEN OSMAN
Dermatology Department, Hopital La Rabta
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KUBISCH Christian
Institute of Human Genetics, University Hospital Cologne
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MOKNI Mourad
"Hereditary Keratinization Disorders" Research Unit, Hopital La Rabta de Tunis
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CHARFEDDINE Cherine
Research Unit (MIGOD), Institut Pasteur de Tunis
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KASSAR Selma
Research Unit, Hopital La Rabta de Tunis
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ZRIBI Hela
Service de Dermatologie, Hopital de la Rabta de Tunis
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BOUCHLAKA Chiraz
Research Unit (MIGOD), Institut Pasteur de Tunis
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REBAI Ahmed
Service de Bioinformatique, Centre de Biotechnologie de Sfax
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OSMAN Amel
Research Unit, Hopital La Rabta de Tunis
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ABDELHAK Sonia
Research Unit (MIGOD), Institut Pasteur 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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Kassar Selma
Service D'anatomo-pathologie 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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Zribi Hela
Service De Dermatologie Hopital De La Rabta De Tunis
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Dhahri-ben Osman
Dermatology Department Hopital La Rabta
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Nouira Sonia
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur 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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Bouchlaka Chiraz
Molecular Investigation Of Genetic Orphan Diseases Institut Pasteur De Tunis
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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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Hanchi Imen
Dermatology Department Hopital La Rabta
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Bchetnia Mbarka
Molecular Investigation Of Genetic Orphan Diseases" Research Unit Institut Pasteur De Tunis
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Kubisch Christian
Institute Of Human Genetics University Hospital Cologne
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Tounsi-guettiti Haifa
Pathology Department Institut Pasteur De Tunis
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Ouragini Houyem
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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Abdelhak Sonia
Research Unit Of Molecular Investigation Of Genetic Orphan Diseases Ur04sp03 Pasteur Institute
著作論文
- Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
- Clinical, histological and genetic investigation of Buschke-Fischer-Brauer's disease in Tunisian families
- Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region