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Publications by Mohammed H. AL-Qahtani
The Evaluation of DiGeorge Syndrome Gene Deletion Using Molecular Cytogenetic Techniques
BMC Genomics
Biotechnology
Genetics
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Recurrence of DiGeorge Syndrome: Prenatal Detection by FISH of a Molecular 22q11 Deletion.
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Molecular Cytogenetic Study of the Nf2 Gene Deletion in Meningioma in Sudanese Patients
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Molecular Cytogenetic Evaluation of Xq Deletion Mosaicism in a Case of Primary Amenorrhea
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DiGeorge Syndrome (Chromosome 22q11.2 Deletion Syndrome): A Historical Perspective With Review of 66 Patients
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In the Line-Up: Deleted Genes Associated With DiGeorge/22q11.2 Deletion Syndrome: Are They All Suspects?
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Myeloproliferative Hypereosinophilic Syndrome: Retrospective Analysis of Cytogenetic and Molecular Features
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HIRA, a DiGeorge Syndrome Candidate Gene, Is Required for Cardiac Outflow Tract Septation
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Treatment Challenges of Refractory Thrombocytopenia in DiGeorge Syndrome
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