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Search Results - Sefiani, Said
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La prise de decision de lancement d’alerte : quels cadres theoriques pour les Sciences de Gestion ?
by
Sefiani, Saïd
Published in
Vie & sciences de l'entreprise
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Expérimentation d’une matrice RST (Responsabilité Sociale des Territoires) auprès d’une association utilisant la boxe comme support de lien social
by
Goujon Belghit, Anne
,
Husser, Jocelyn
,
Cuénoud, Thibault
,
Sefiani, Saïd
Published in
La revue des sciences de gestion
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Synthesis and pyrolysis of organometallic precursors of SiCGe alloy amorphous thin films
by
Mazerolles, Pierre
,
Reynes, Alex
,
Sefiani, Said
,
Morancho, Roland
Published in
Journal of analytical and applied pyrolysis
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Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature
by
Zrhidri, Abdelali
,
Jaouad, Imane Cherkaoui
,
Lyahyai, Jaber
,
Raymond, Laure
,
Egéa, Grégory
,
Taoudi, Mohamed
,
El Mouatassim, Said
,
Sefiani, Abdelaziz
Published in
Gene
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IoT-Based Data Logger for solar systems applications
by
Rerhrhaye, Fathallah
,
Lahlouh, Ilyas
,
Ennaciri, Yassine
,
Benzazah, Chirine
,
El Akkary, Ahmed
,
Sefiani, Nacer
,
Bouftane, Said
Published in
ITM web of conferences
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A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report
by
Cherkaoui Jaouad, Imane
,
Zrhidri, Abdelali
,
Jdioui, Wafaa
,
Lyahyai, Jaber
,
Raymond, Laure
,
Egéa, Grégory
,
Taoudi, Mohamed
,
El Mouatassim, Said
,
Sefiani, Abdelaziz
Published in
BMC medical genetics
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Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
by
Adadi, Najlae
,
Sahli, Maryem
,
Egéa, Grégory
,
Ratbi, Ilham
,
Taoudi, Mohamed
,
Zniber, Layla
,
Jdioui, Wafaa
,
El Mouatassim, Said
,
Sefiani, Abdelaziz
Published in
Journal of medical case reports
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Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease
by
Zrhidri, Abdelali
,
Amasdl, Saadia
,
Lyahyai, Jaber
,
Elouardi, Hanane
,
Chkirate, Bouchra
,
Raymond, Laure
,
Egéa, Grégory
,
Taoudi, Mohamed
,
El Mouatassim, Said
,
Sefiani, Abdelaziz
Published in
Pediatric rheumatology online journal
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Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome
by
Baziz, Meriem
,
Hamouli-Said, Zohra
,
Ratbi, Ilham
,
Habel, Mohamed
,
Guaoua, Soukaina
,
Sbiti, Aziza
,
Sefiani, Abdelaziz
Published in
Iranian journal of public health
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Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies
by
Natiq, Abdelhafid
,
Elalaoui, Siham Chafai
,
Liehr, Thomas
,
Amzazi, Saïd
,
Sefiani, Abdelaziz
Published in
Indian journal of human genetics
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Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies
by
Natiq, Abdelhafid
,
Elalaoui, Siham Chafai
,
Liehr, Thomas
,
Amzazi, Saïd
,
Sefiani, Abdelaziz
Published in
Indian journal of human genetics
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