Genotype-phenotype correlation in 22q11.2 deletion syndrome
<p>Abstract</p> <p>Background</p> <p>The 22q11.2 deletion syndrome (22q11.2DS) is caused by hemizygous microdeletions on chromosome 22q11.2 with highly variable physical and neuropsychiatric manifestations. We explored the genotype-phenotype relationship in a relatively...
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Main Authors: | Michaelovsky Elena (Author), Frisch Amos (Author), Carmel Miri (Author), Patya Miriam (Author), Zarchi Omer (Author), Green Tamar (Author), Basel-Vanagaite Lina (Author), Weizman Abraham (Author), Gothelf Doron (Author) |
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Format: | Book |
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BMC,
2012-12-01T00:00:00Z.
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