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1دورية أكاديمية
المؤلفون: Abdelhamid Bouramtane, Fatima Zahra Moufid, Mohamed Ahakoud, Laila Bouguenouch, Karim Ouldim
المصدر: Genetics in Medicine Open, Vol 1, Iss 1, Pp 100065- (2023)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Achraf El Asri, Karim Ouldim, Laila Bouguenouch, Mohammed Sekal, Fatima Zahra Moufid, Ellen Kampman, Inge Huybrechts, Marc J. Gunter, Sanae Abbaoui, Kaoutar Znati, Mehdi Karkouri, Khaoula El Kinany, Zineb Hatime, Meimouna Mint Sidi Deoula, Laila Chbani, Btissame Zarrouq, Karima El Rhazi
المصدر: Nutrients, Vol 14, Iss 2, p 318 (2022)
مصطلحات موضوعية: colorectal cancer, KRAS mutations, diet, fat intake, Moroccan population, Nutrition. Foods and food supply, TX341-641
وصف الملف: electronic resource
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3
المؤلفون: Mohamed Iraqui Houssaini, Ihssane El Bouchikhi, Laila Bouguenouch, Karim Ouldim, Fatima Zahra Moufid
المصدر: The Turkish Journal of Gastroenterology. :701-704
مصطلحات موضوعية: Genetic Markers, 0301 basic medicine, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Genetic counseling, Case Report, Cecal Neoplasms, MLH1, Frameshift mutation, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Gene duplication, medicine, Humans, Genetic Predisposition to Disease, Frameshift Mutation, Germ-Line Mutation, Genetics, business.industry, Gastroenterology, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Pedigree, Morocco, 030104 developmental biology, MSH2, 030220 oncology & carcinogenesis, Female, MutL Protein Homolog 1, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9644a12c4d54874a0ab4e1a10f6af875
https://doi.org/10.5152/tjg.2018.17761 -
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المؤلفون: Hanan El Ouahabi, Fatima Zahra Moufid, Hanane Latrech, Karim Ouldim, Bahia Bennani, Ihssane El Bouchikhi, Sana Abourazzak, Nadia Maazouzi, Laila Bouguenouch, Salma Benyakhlef, Lahsen El Ghadraoui, Said Trhanint
المصدر: International journal of pediatricsadolescent medicine. 9(2)
مصطلحات موضوعية: Genetics, Sanger sequencing, business.industry, Disease, medicine.disease, Asymptomatic, Maturity onset diabetes of the young, HNF1A, symbols.namesake, Diabetes mellitus, Pediatrics, Perinatology and Child Health, medicine, symbols, Missense mutation, Multiplex ligation-dependent probe amplification, medicine.symptom, business
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المؤلفون: Mohamed Iraqui Houssaini, Laila Bouguenouch, Karim Ouldim, Bahia Bennani, Laila Chbani, Fatima Zahra Moufid, Ihssane El Bouchikhi, Mohamed Sekal, Khadija Belhassan
المصدر: Genetic Testing and Molecular Biomarkers. 22:492-497
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Colorectal cancer, DNA Mutational Analysis, MLH1, DNA Mismatch Repair, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Internal medicine, Prevalence, medicine, Humans, Genetic Predisposition to Disease, Gene, Early Detection of Cancer, Germ-Line Mutation, Genetics (clinical), Aged, Aged, 80 and over, Molecular screening, business.industry, General Medicine, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Morocco, MutS Homolog 2 Protein, Increased risk, MSH2, 030220 oncology & carcinogenesis, Female, 030211 gastroenterology & hepatology, Age of onset, Colorectal Neoplasms, MutL Protein Homolog 1, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ec5c8fede2f12d225079f07c395c8f
https://doi.org/10.1089/gtmb.2018.0067 -
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المؤلفون: M. Hida, Laila Bouguenouch, Driss Couissi, Jamila El-Akhal, Ihssane El Bouchikhi, Karim Ouldim, Hanane Sayel, Touhami Mejtoute, Fatima Zahra Moufid
المصدر: Human Genome Variation. 4
مصطلحات موضوعية: 0301 basic medicine, Genetics, business.industry, Familial Mediterranean fever, medicine.disease, MEFV, Biochemistry, Pyrin domain, 03 medical and health sciences, Exon, 030104 developmental biology, 0302 clinical medicine, Mutation (genetic algorithm), Gene duplication, Medicine, Insertion, business, Molecular Biology, 030217 neurology & neurosurgery, Exome sequencing