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mlpa
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1 Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes.
2 prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18
3 detección de un caso de síndrome de williams-beuren por mlpa
4 sÍndrome de digeorge/velocardiofacial: resultados do laboratÓrio de citogenÉtica do cgmjm por tÉcnicas de fish e mlpa
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