Brockington, M., Sewry, C. A., Herrmann, R., Naom, I., Dearlove, A., Rhodes, M., . . . Muntoni, F. (2000). Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42. The American Society of Human Genetics.
Citación estilo ChicagoBrockington, Martin, et al. Assignment of a Form of Congenital Muscular Dystrophy With Secondary Merosin Deficiency to Chromosome 1q42. The American Society of Human Genetics, 2000.
Cita MLABrockington, Martin, et al. Assignment of a Form of Congenital Muscular Dystrophy With Secondary Merosin Deficiency to Chromosome 1q42. The American Society of Human Genetics, 2000.
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