Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę ""Al-Mutairi, Fuad"" wg kryterium: Autor


Wyświetlanie 1-8 z 8
Tytuł:
What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations.
Autorzy:
Alfares A; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia. .; Department of Pediatrics, College of Medicine, Qassim University, Qassim, Saudi Arabia. .; Qassim University, Department of Pediatrics, Almulyda, Saudi Arabia. .
Alsubaie L; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Aloraini T; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Alaskar A; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Althagafi A; Computer, Electrical & Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Alahmad A; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Rashid M; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Alswaid A; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Alothaim A; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Eyaid W; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Ababneh F; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Albalwi M; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Alotaibi R; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Almutairi M; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Altharawi N; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Alsamer A; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdelhakim M; Computer, Electrical & Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Kafkas S; Computer, Electrical & Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Mineta K; Computer, Electrical & Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Cheung N; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Abdallah AM; Department of Basic Medical Sciences, College of Medicine, QU Health, Qatar University, Doha, Qatar.
Büchmann-Møller S; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Fukasawa Y; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Zhao X; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Rajan I; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Hoehndorf R; King Abdullah University of Science and Technology (KAUST), Core Labs, Thuwal, 23955-6900, Saudi Arabia.
Al Mutairi F; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Gojobori T; Biological and Environmental Science and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Alfadhel M; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.; King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Pokaż więcej
Źródło:
BMC medical genomics [BMC Med Genomics] 2020 Jul 17; Vol. 13 (1), pp. 103. Date of Electronic Publication: 2020 Jul 17.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
Consanguinity*
Exome*
Family*
Genetic Markers*
Genetic Predisposition to Disease*
Genetic Testing*
Genetic Variation*
Adult ; Child ; Female ; Humans ; Male ; Retrospective Studies ; Exome Sequencing
Czasopismo naukowe
Tytuł:
Expanding the phenotype of PPP1R21‐related neurodevelopmental disorder.
Autorzy:
Almannai, Mohammed (AUTHOR)
Marafi, Dana (AUTHOR)
Zaki, Maha S. (AUTHOR)
Maroofian, Reza (AUTHOR)
Efthymiou, Stephanie (AUTHOR)
Saadi, Nebal Waill (AUTHOR)
Filimban, Bilal (AUTHOR)
Dafsari, Hormos Salimi (AUTHOR)
Rahman, Fatima (AUTHOR)
Maqbool, Shazia (AUTHOR)
Faqeih, Eissa (AUTHOR)
Al Mutairi, Fuad (AUTHOR)
Alsharhan, Hind (AUTHOR)
Abdelaty, Omar (AUTHOR)
Bin‐Hasan, Saadoun (AUTHOR)
Duan, Ruizhi (AUTHOR)
Noureldeen, Mahmoud M. (AUTHOR)
Alqattan, Alaa (AUTHOR)
Houlden, Henry (AUTHOR)
Hunter, Jill V. (AUTHOR)
Pokaż więcej
Źródło:
Clinical Genetics. Feb2024, p1. 10p. 4 Illustrations, 1 Chart.
Czasopismo naukowe
    Wyświetlanie 1-8 z 8

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies