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Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary and Mohammad H. Al-Qahtani
Neurosciences Journal October 2018, 23 (4) 346-350; DOI: https://doi.org/10.17712/nsj.2018.4.20180095
Muhammad I. Naseer
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
M.phil, PhDMahmood Rasool
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhDAngham A. Abdulkareem
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhD studentRanda I. Bassiouni
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
MDHussein Algahtani
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
MD, FRCPSAdeel G. Chaudhary
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhDMohammad H. Al-Qahtani
From the Center of Excellence in Genomic Medicine Research (Naseer, Rasool Abdulkareem, Chaudhary, Al-Qahtan) King Abdulaziz University, and from King Abdulaziz Medical City (Algahtani), King Saud bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia, and from Clinical Genetic Division of Human Genetics & Genome Research, National Research Center (Bassiouni), Dokki, Giza, Egypt
PhDReferences
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In this issue
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary, Mohammad H. Al-Qahtani
Neurosciences Journal Oct 2018, 23 (4) 346-350; DOI: 10.17712/nsj.2018.4.20180095
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
Muhammad I. Naseer, Mahmood Rasool, Angham A. Abdulkareem, Randa I. Bassiouni, Hussein Algahtani, Adeel G. Chaudhary, Mohammad H. Al-Qahtani
Neurosciences Journal Oct 2018, 23 (4) 346-350; DOI: 10.17712/nsj.2018.4.20180095
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