المؤلفون: EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Bouguenouch, Laila, Samri, Imane, Iraqui Houssaïni, Mohammed, Ouldim, Karim, Atmani, Samir

المساهمون: Hassan II University Hospital of Fez, Faculty of Medicine and Pharmacy of Fez

المصدر: Egyptian Journal of Medical Human Genetics ; volume 22, issue 1 ; ISSN 2090-2441

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1186/s43042-021-00136-1Test

المؤلفون: El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Samri, Imane, Abdouss, Fatima, Melhouf, Moulay Abdelilah, Iraqui Houssaini, Mohammed, Belhassan, Khadija, Atmani, Samir, Ouldim, Karim

المساهمون: Hassan II University Hospital of Fez

المصدر: Egyptian Journal of Medical Human Genetics ; volume 21, issue 1 ; ISSN 2090-2441

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1186/s43042-020-0047-9Test

المؤلفون: EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Bouguenouch, Laila, Samri, Imane, Bouhrim, Mohamed, Ouldim, Karim, Atmani, Samir

المصدر: African Health Sciences; Vol 18, No 4 (2018); 922-930 ; 1680-6905

مصطلحات موضوعية: Tetralogy of Fallot, GATA4, molecular screening, risk factors

وصف الملف: application/pdf

العلاقة: https://www.ajol.info/index.php/ahs/article/view/180224/169570Test; https://www.ajol.info/index.php/ahs/article/view/180224Test

الإتاحة: https://www.ajol.info/index.php/ahs/article/view/180224Test

المؤلفون: El Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Houssaini, Mohammed Iraqui, Bouguenouch, Laila, Samri, Imane, Atmani, Samir, Ouldim, Karim

المصدر: International Journal of Pediatrics and Adolescent Medicine ; volume 3, issue 4, page 133-142 ; ISSN 2352-6467

الإتاحة: https://doi.org/10.1016/j.ijpam.2016.06.003Test
https://api.elsevier.com/content/article/PII:S2352646716300321?httpAccept=text/plainTest
https://api.elsevier.com/content/article/PII:S2352646716300321?httpAccept=text/xmlTest
https://journals.lww.com/01863514-201603040-00001Test

المؤلفون: El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Belhassan, Khadija, Samri, Imane, Chaouti, Amal, Houssaïni, Mohammed Iraqui, Atmani, Samir, Ouldim, Karim

المصدر: Eurasian Journal of Medicine; Oct2020, Vol. 52 Issue 3, p283-287, 5p

مصطلحات موضوعية: DNA analysis, ALGORITHMS, ATRIAL septal defects, CONGENITAL heart disease, LONGITUDINAL method, GENETIC mutation, POLYMERASE chain reaction, TETRALOGY of Fallot, TRANSCRIPTION factors, GENETIC testing, DATA analysis software, DESCRIPTIVE statistics, SEQUENCE analysis

مصطلحات جغرافية: MOROCCO

المؤلفون: Bouguenouch, Laila, Samri, Imane, Belhassan, Khadija, Sayel, Hanane, Abbassi, Meriame, Bennis, Sanae, Benajah, Dafr Allah, Ibrahimi, Adil, Amarti, Afaf, Ouldim, Karim

المصدر: Pan African Medical Journal; Vol 24, No 1 (2016) ; 1937-8688

العلاقة: http://www.ajol.info/index.php/pamj/article/view/144019Test

الإتاحة: http://www.ajol.info/index.php/pamj/article/view/144019Test

المؤلفون: BOUCHIKHI, IHSSANE EL, SAMRI, IMANE, HOUSSAINI, MOHAMMED IRAQUI, TRHANINT, SAAID, BOUGUENOUCH, LAILA, SAYEL, HANANE, HIDA, MOUSTAPHA, ATMANI, SAMIR, OULDIM, KARIM

المصدر: Turkish Journal of Medical Sciences

مصطلحات موضوعية: Noonan syndrome, PTPN11, mutation analysis, SHP-2, mutation rate comparison, Medical Sciences

وصف الملف: application/pdf

العلاقة: https://journals.tubitak.gov.tr/medical/vol45/iss2/8Test; https://journals.tubitak.gov.tr/context/medical/article/2849/viewcontent/sag_45_2_8_1310_50.pdfTest

الإتاحة: https://doi.org/10.3906/sag-1310-50Test
https://journals.tubitak.gov.tr/medical/vol45/iss2/8Test
https://journals.tubitak.gov.tr/context/medical/article/2849/viewcontent/sag_45_2_8_1310_50.pdfTest

المؤلفون: Janati Idrissi, Meryem, Samri, Imane, Khabbal, Youssef, El Hassouni, Mohammed, Ouldim, Karim

المصدر: Clinics and Research in Hepatology and Gastroenterology ; volume 39, issue 4, page e55-e56 ; ISSN 2210-7401

مصطلحات موضوعية: Gastroenterology, Hepatology

الإتاحة: https://doi.org/10.1016/j.clinre.2014.11.002Test
https://api.elsevier.com/content/article/PII:S2210740114002873?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2210740114002873?httpAccept=text/plainTest

العنوان البديل: Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases.

المؤلفون: Bouguenouch, Laila¹, Samri, Imane¹, Abbassi, Meryem¹, Hamdaoui, Hasna¹, El Otmani, Ihssane¹, Sayel, Hanane¹, Trhanint, Said¹, Benmiloud, Sara^2,3, Amrani, Moncif^2,4, Bennis, Sanae^1,2, Ouldim, Karim^1,2, Hida, Mustapha^2,3

المصدر: Pan African Medical Journal. 2017, Vol. 28, p1-8. 8p.

المؤلفون: Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

المصدر: The Pan African Medical Journal, Vol 11, Iss 3 (2012)
Pan African Medical Journal; Vol 11, No 1 (2012)
The Pan African Medical Journal

مصطلحات موضوعية: Williams Syndrome, fish, lcsh:R5-920, 22q11 Deletion Syndrome, lcsh:Public aspects of medicine, Infant, Genetic Counseling, lcsh:RA1-1270, Syndromes microdélétionnels, FISH, Syndrome de Williams, 22q11, syndromes microdélétionnels, 22q11, Cytogenetics, Humans, Case Series, Female, Child, lcsh:Medicine (General), syndrome de williams

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4b0dac6b1fc92ab48bc3c90025843643Test
https://doaj.org/article/387eb3e453944dfab9b6ce6eaa9baf23Test