An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14)
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Published in American journal of medical genetics. Part A (01.04.2012)
Published in American journal of medical genetics. Part A (01.04.2012)
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A CRYGC gene mutation associated with autosomal dominant pulverulent cataract
González-Huerta, Luz Ma, Messina-Baas, Olga, Urueta, Héctor, Toral-López, Jaime, Cuevas-Covarrubias, Sergio A.
Published in Gene (15.10.2013)
Published in Gene (15.10.2013)
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