Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome
<p>Abstract</p> <p>Background</p> <p>Chromosome 22q11 deletion syndrome (22q11DS) causes a developmental disorder during the embryonic stage, usually because of hemizygous deletions. The clinical pictures of patients with 22q11DS vary because of polymorphisms: on averag...
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Principais autores: | , , , , , , , , , |
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Formato: | Livro |
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BMC,
2009-02-01T00:00:00Z.
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Número de Chamada: |
A1234.567 |
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