Revista Chilena de Pediatría
 2016
DOI: 10.1016/j.rchipe.2016.04.010
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Un caso de deleción parcial 1p36.1 y trisomía parcial 6p diagnosticadas por cariotipo

Monica Fernández Pineda
1
,
Julián Ramírez-Cheyne
2
,
Carolina Isaza
3
et al.

Abstract: The development of new techniques in molecular biology has improved diagnostic possibilities in medical genetics. However, the traditional karyotype remains as an important diagnostic tool in patients with multiple congenital anomalies.

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