Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hasna Hamdaoui

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Cureus|August 9, 2021
Report of a New Case of Pentasomy X Revealed by Status EpilepticusNabila Chekhlabi, Amal Haoudar, Hasna Hamdaoui, et al.
Bioinformatics and Biology Insights|August 12, 2022
Multiple Myeloma: Bioinformatic Analysis for Identification of Key Genes and PathwaysChaimaa Saadoune, Badreddine Nouadi, Hasna Hamdaoui, et al.
Clinical Case Reports|March 28, 2022
Detection of a new deleterious <i>SGCE</i> gene variant in Moroccan family with inherited myoclonus-dystoniaFaiza Chbel, Hicham Charroute, Redouane Boulouiz, et al.
Leukemia Research Reports|August 8, 2020
Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myelomaHasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, et al.
Leukemia Research Reports|November 30, 2023
Cytogenetic abnormalities correlate with clinico-biological characteristics in 30 Moroccan multiple myeloma patientsHasna Hamdaoui, Badreddine Nouadi, Oumaima Benlarroubia, et al.
The Pan African Medical Journal|February 28, 2012
[The Cri du Chat syndrome: report of an observation]Karim Ouldim, Imane Samri, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
The Pan African Medical Journal|February 28, 2012
[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations]Karim Ouldim, Laila Bouguenouch, Imane Samri, et al.
Molecular Genetics & Genomic Medicine|June 24, 2020
Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patientsHasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, et al.
The Pan African Medical Journal|June 27, 2018
[Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases]Laila Bouguenouch, Imane Samri, Meryem Abbassi, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Cureus|August 9, 2021
Report of a New Case of Pentasomy X Revealed by Status EpilepticusNabila Chekhlabi, Amal Haoudar, Hasna Hamdaoui, et al.
Bioinformatics and Biology Insights|August 12, 2022
Multiple Myeloma: Bioinformatic Analysis for Identification of Key Genes and PathwaysChaimaa Saadoune, Badreddine Nouadi, Hasna Hamdaoui, et al.
Clinical Case Reports|March 28, 2022
Detection of a new deleterious <i>SGCE</i> gene variant in Moroccan family with inherited myoclonus-dystoniaFaiza Chbel, Hicham Charroute, Redouane Boulouiz, et al.
Leukemia Research Reports|August 8, 2020
Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myelomaHasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, et al.
Leukemia Research Reports|November 30, 2023
Cytogenetic abnormalities correlate with clinico-biological characteristics in 30 Moroccan multiple myeloma patientsHasna Hamdaoui, Badreddine Nouadi, Oumaima Benlarroubia, et al.
The Pan African Medical Journal|February 28, 2012
[The Cri du Chat syndrome: report of an observation]Karim Ouldim, Imane Samri, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
The Pan African Medical Journal|February 28, 2012
[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations]Karim Ouldim, Laila Bouguenouch, Imane Samri, et al.
Molecular Genetics & Genomic Medicine|June 24, 2020
Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patientsHasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, et al.
The Pan African Medical Journal|June 27, 2018
[Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases]Laila Bouguenouch, Imane Samri, Meryem Abbassi, et al.
Pageof 1