Deleção do cromossomo 9 na região q22q32 em bebê com cariótipo 46XY: relato de um caso Deletion of chromosome 9 in the region q22q32 in a male baby with karyotype 46XY: report of a case
Este trabalho teve como objetivo o estudo laboratorial e por imagem das malformações de um bebê do sexo masculino que apresentou, por ocasião do parto, prematuridade, cardiopatia congênita, insuficiência respiratória e malformação congênita. O estudo ecográfico gestacional mostrou o osso...
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Main Authors: | Seme Youssef Reda (Author), Jean Ricardo Nicareta (Author) |
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Format: | Book |
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Sociedade Brasileira de Patologia Clínica,
2008-10-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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