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Issue Date	Title	Author(s)
2013	Roˆle potentiel du facteur angioge´nique « EG-VEGF » dans les maladies gestationnelles trophoblastiques	Boufettal, Houssine; Feige, Jean-Jacques; Benharouga, Mohamed; Aboussaouira, Touria; Nadifi, Sellama; Mahdaoui, Sakher; Samouh, Naima; Alfaidy, Nadia
2013	Profil épidémiologique des cancers de la cavité orale et de la lèvre inférieure au service de stomatologie et chirurgie maxillofaciale de l’hôpital du 20-Août, CHU Ibn-Rochd de Casablanca	Slimani, F.; Nadifi, Sellama; Oukerroum, A.; Chekkoury-Idrissi, A.; Aboussaouira, Touria; Belhallaj, M.
2009	The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population	Dieterich, Klaus; Zouari, Raoudha; Harbuz, Radu; Vialard, Franc¸ois; Martinez, Delphine; Bellayou, Hanane; Prisant, Nadia; Zoghmar, Abdelali; Guichaoua, Marie Roberte; Koscinski, Isabelle; Kharouf, Mahmoud; Noruzinia, Mehrdad; Nadifi, Sellama; Sefiani, Abdelaziz; Lornage, Jacqueline; Zahi, Mohamed; Viville, Ste´phane; Se`le, Bernard; Jouk, Pierre-Simon; Jacob, Marie-Christine; Escalier, Denise; Nikas, Yorgos; Hennebicq, Sylviane; Lunardi, Joe¨l; F. Ray, Pierre
2017	A genetic overview of Atlantic coastal populations from Europe and North-West Africa based on a 17 X-STR panel	Prieto-Fernández, Endika; Díaz-de Usera, Ana; Baeta, Miriam; Núñez, Carolina; Chbel, Faiza; Nadifi, Sellama; Rouault, Karen; Férec, Claude; Hardiman, Orla; Pinheiro, Fátima; M. de Pancorbo, Marian
2016	Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population	Marouf, Chaymaa; Göhler, Stella; Da Silva Filho, Miguel Inacio; Hajji, Omar; Hemminki, Kari; Nadifi, Sellama; Försti, Asta
2003	Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS a protein that associates with the USH1C protein harmonin	Weil, Dominique; El-Amraoui, Aziz; Masmoudi, Saber; Mustapha, Mirna; Kikkawa, Yoshiaki; Laine, Sophie; Delmaghani, Sedigheh; Adato, Avital; Nadifi, Sellama; Ben Zina, Zeineb; Hamel, Christian; Gal, Andreas; Ayadi, Hammadi; Yonekawa, Hiromichi; Petit, Christine
2015	A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: Case report	Karkar, Adnane; Barakat, Abdelhamid; Bakhchane, Amina; Fettah, Houda; Slassi, Ilham; Dorboz, Imen; Boespflug-Tanguy, Odile; Nadifi, Sellama
2003	Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework.	Chbel, Faiza; Nadifi, Sellama; Martinez-Bouzas, Cristina; Louahlia, Said; Azeddoug, Houssine; Martinez De Pancorbo, Marian
2014	Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels	Sassi, Atfa; Lazaroski, Sandra; Wu, Gang; M. Haslam, Stuart; Fliegauf, Manfred; Mellouli, Fethi; Patiroglu, Turkan; Unal, Ekrem; Akif Ozdemir, Mehmet; Jouhadi, Zineb; Khadir, Khadija; Ben-Khemis, Leila; Ben-Ali, Meriem; Ben-Mustapha, Imen; Borchani, Lamia; Pfeifer, Dietmar; Jakob, Thilo; Khemiri, Monia; Asplund, A. Charlotta; O. Gustafsson, l Manuela; E. Lundin, l Karin; Falk-Sorqvist, l Elin; N. Moens, Lotte; Eke Gungor, Hatice; R. Engelhardt, Karin; Dziadzio, Magdalena; Stauss, Hans; Fleckenstein, Bernhard; Meier, Rebecca; Prayitno, Khairunnadiya; Maul-Pavicic, Andrea; Schaffer, Sandra; Rakhmanov, Mirzokhid; Henneke, Philipp; Kraus, Helene; Eibel, Hermann; Kolsch, Uwe; Nadifi, Sellama; Nilsson, Mats; Bejaoui, Mohamed; A. Schaffer, Alejandro; Smith, Edvard; Dell, Anne; Barbouche, Mohamed-Ridha; Grimbacher, Bodo
2013	Sickle cell disease with double stroke in a moroccan family	Hamzi, Khalil; Ben Itto, Afaf; Jouhadi, Zineb; Slassi, Ilham; Nadifi, Sellama