Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome von Chbel, Faiza, Hamdaoui, Hasna, Mossafa, Houssein, Ouldim, Karim, Benrahma, Houda

Volltext

Multiple Myeloma: Bioinformatic Analysis for Identification of Key Genes and Pathways von Saadoune, Chaimaa, Nouadi, Badreddine, Hamdaoui, Hasna, Chegdani, Fatima, Bennis, Faiza

Volltext

Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia von Chbel, Faiza, Charroute, Hicham, Boulouiz, Redouane, Hamdaoui, Hasna, Mossafa, Houssein, Benrahma, Houda, Ouldim, Karim

Volltext

Cytogenetic Abnormalities Correlate With Clinico-Biological Characteristics in 30 Moroccan Multiple Myeloma Patients von Hamdaoui, Hasna, Nouadi, Badreddine, Benlarroubia, Oumaima, Chbel, Faiza, Saadoune, Chaimaa, Bennis, Faïza, Lamzouri, Afaf, Chegdani, Fatima

Volltext

Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma von Hamdaoui, Hasna, Natiq, Abdelhafid, Benlarroubia, Oumaima, Liehr, Thomas, Dehbi, Hind, Loukhmas, Latifa, Chegdani, Fatima

Volltext

Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients von Hamdaoui, Hasna, Benlarroubia, Oumaima, Ait Boujmia, Oum Kaltoum, Mossafa, Hossein, Ouldim, Karim, Belkhayat, Aziza, Smyej, Imane, Benrahma, Houda, Dehbi, Hind, Chegdani, Fatima

Volltext

Report of a New Case of Pentasomy X Revealed by Status Epilepticus von Chekhlabi, Nabila, Haoudar, Amal, Hamdaoui, Hasna, Dini, Nezha

Volltext

Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations von Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, Otmani, Ihssane El, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha

Volltext

Marqueurs chromosomiques: à propos d'un cas von Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, El Otmani, Ihsan, El Omairi, Nissrine, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim

Volltext

Le syndrome de Cri du Chat : A propos d’une observation von Ouldim, Karim, Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Hbibi, Mohamed, Chaouki, Sana, Hida, Moustapha

Volltext

Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations von Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

Volltext

Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases von Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, Otmani, Ihssane El, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha

Volltext

Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations von Bouguenouch, Laila, Samri, Imane, Abbassi, Meryem, Hamdaoui, Hasna, El Otmani, Ihssane, Sayel, Hanane, Trhanint, Said, Benmiloud, Sara, Amrani, Moncif, Bennis, Sanae, Ouldim, Karim, Hida, Mustapha

Volltext

Marqueurs chromosomiques: à propos d'un cas von Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Omairi, Nissrine El, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim

Volltext

Report of a New Case of Pentasomy X Revealed by Status Epilepticus von Chekhlabi, Nabila, Haoudar, Amal, Hamdaoui, Hasna, Dini, Nezha

Volltext

Cytogenetic abnormalities correlate with clinico-biological characteristics in 30 Moroccan multiple myeloma patients von Hamdaoui, Hasna, Nouadi, Badreddine, Benlarroubia, Oumaima, Chbel, Faiza, Saadoune, Chaimaa, Bennis, Faïza, Lamzouri, Afaf, Chegdani, Fatima

Volltext

Chromosome markers: case report von Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, El Otmani, Ihsan, El Omairi, Nissrine, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim

Volltext

The Cri du Chat syndrome: report of an observation von Ouldim, Karim, Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Hbibi, Mohamed, Chaouki, Sana, Hida, Moustapha

Volltext

Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma von Hamdaoui, Hasna, Natiq, Abdelhafid, Benlarroubia, Oumaima, Liehr, Thomas, Dehbi, Hind, Loukhmas, Latifa, Chegdani, Fatima

Volltext

Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations von Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

Volltext