Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sarah A. Ababtain"'
Autor:
Mohrah A. Alalshaikh, Ammar H. Alsughayir, Alyazeed S. Alsaif, Sarah A. Ababtain, Shaika Y. Aloyouni, Khawlah E. Aldilaijan, Sahar F. Alsubaie
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 12, Iss 3, Pp 210-215 (2024)
Background: The RHD gene is one of the most complex blood group genes. The molecular background of the RHD gene in RhD-negative and RhD-positive individuals varies within and among different populations. Knowing the molecular basis of the RHD gene in
Externí odkaz:
https://doaj.org/article/139905b61cd64ae295aa37d31371d165
Autor:
Nader Alrahili, Mansour Abdulaziz Al Harthi, Sarah Jassim Ababtain, Salma Saad Al Sharif, Mohammed Abdulaziz Alnuwaysir, Roaa Fahad Al Huzaimi
Publikováno v:
Psych, Vol 4, Iss 2, Pp 238-246 (2022)
The present study was designed to investigate attitudes and beliefs among parents of patients with attention deficit hyperactivity disorder (ADHD), with regard to symptoms, causes, prognosis, and management. The study was of a cross-sectional descrip
Externí odkaz:
https://doaj.org/article/ed7f3d9fbff24556a670cf5b6181c764
Autor:
Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-10 (2024)
Abstract Background Chromosome 16p11.2 deletions and duplications were found to be the second most common copy number variation (CNV) reported in cases with clinical presentation suggestive of chromosomal syndromes. Chromosome 16p11.2 deletion syndro
Externí odkaz:
https://doaj.org/article/c35507dced82439484a71711a4834fd0
Autor:
Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/e24a3331985f49f8bdc8961b2c06b84b