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Publications by A Oohira
Deletion of a Single Chromosome Band 4q26 in a Malformed Girl: Exclusion of Rieger Syndrome Associated Gene(s) From the 4q26 Segment.
Journal of Medical Genetics
Genetics
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Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome
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Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
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Gene Expression From the Aneuploid Chromosome in a Trisomy Mouse Model of Down Syndrome
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DiGeorge Syndrome (Chromosome 22q11.2 Deletion Syndrome): A Historical Perspective With Review of 66 Patients
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Chromosome 10q26 Deletion Syndrome: Two New Cases and a Review of the Literature
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Infantile Spasms Is Associated With Deletion of the MAGI2 Gene on Chromosome 7q11.23-Q21.11
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Axenfeld Rieger Syndrome: A Rare Case Report of Two Siblings
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