Որոնման արդյունքները - Salwa Alkhalifi
- Ցուցադրվում են 1 - 3 արդյունքները 3
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1
Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability Francjan J. van Spronsen, Nastassja Himmelreich, Véronique Rüfenacht, Nan Shen, Danique van Vliet, Mohammed Al‐Owain, Khushnooda Ramzan, Salwa Alkhalifi, Roelineke J. Lunsing, Rebecca Heiner‐Fokkema, Anahita Rassi, Corinne Gemperle-Britschgi, Georg F. Hoffmann, Nenad Blau, Beat Thöny
Հրապարակվել է 2017Artigo -
2
Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases Lama AlAbdi, Hanan E. Shamseldin, Ebtissal Khouj, Rana Helaby, Bayan Mohammed Aljamal, Mashael Alqahtani, Aisha Almulhim, Halima Hamid, Mais Hashem, Firdous Abdulwahab, Omar Abouyousef, Amal Jaafar, Tarfa Alshidi, Mohammed Al‐Owain, Amal Alhashem, Saeed Al Tala, Arif O. Khan, Elham Al Mardawi, Hisham Alkuraya, Eissa Faqeih, Manal Afqi, Salwa Alkhalifi, Zuhair Rahbeeni, Samya Hagos, Wijdan Al‐Ahmadi, Seba Nadeef, Sateesh Maddirevula, Khalid S.A. Khabar, Alexander Putra, Angel Angelov, Changsook Park, Ana M. Reyes-Ramos, Husen M. Umer, Ikram Ullah, Patrick Driguez, Yoshinori Fukasawa, Ming Sin Cheung, Imed‐Eddine Gallouzi, Fowzan S. Alkuraya
Հրապարակվել է 2023Artigo -
3
Genomic and phenotypic delineation of congenital microcephaly Ranad Shaheen, Sateesh Maddirevula, Nour Ewida, Saud Alsahli, Ghada M. H. Abdel‐Salam, Maha S. Zaki, Saeed Al Tala, Amal Alhashem, Ameen Softah, Mohammed Al‐Owain, Anas M. Alazami, Basma Abadel, Nisha Patel, Tarfa Al‐Sheddi, Rana Alomar, Eman Alobeid, Niema Ibrahim, Mais Hashem, Firdous Abdulwahab, Muddathir H. Hamad, Brahim Tabarki, Ali H. Alwadei, Fahad Al-Hazzani, Fahad A. Bashiri, Amal Y. Kentab, Serdar Şahintürk, Elliott H. Sherr, Brieana Fregeau, Samira Sogati, Saad AlShahwan, Salwa Alkhalifi, Zainab Alhumaidi, Samia A. Temtamy, Mona Aglan, Ghada A. Otaify, Katta M. Girisha, Maha Tulbah, Mohammed Zain Seidahmed, Mustafa A. Salih, Mohamed Abouelhoda, Afaque A. Momin, Muna Al Saffar, Jennifer N. Partlow, Stefan T. Arold, Eissa Faqeih, Christopher A. Walsh, Fowzan S. Alkuraya
Հրապարակվել է 2018Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Exome
Exome sequencing
Mendelian inheritance
Phenotype
Allele
Amino acid
Bioinformatics
Biopterin
Compound heterozygosity
Computational biology
DNA sequencing
Dwarfism
Dystonia
Endocrinology
Genetic heterogeneity
Genome
Homovanillic acid
Human genetics
Hyperphenylalaninemia
Internal medicine
Locus (genetics)
Microcephaly
Mutation
Neuroscience
Nitric oxide
Nitric oxide synthase