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Browsing by Author MacDonald, Alexandra

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Issue DateTitleAuthor(s)
2015Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to dateMartínez-Fernández, María Luisa; Fernández Toral, Joaquín; Llano Rivas, Isabel; Bermejo-Sánchez, Eva; MacDonald, Alexandra; Martínez-Frías, María Luisa
2014Haploinsufficiency of BMP4 Gene May be the Underlying Cause of Frias SyndromeMartínez-Fernández, María Luisa; Bermejo-Sánchez, Eva; Fernández Colomer, María Belén; MacDonald, Alexandra; Fernández Toral, Joaquín; Martínez-Frías, María Luisa
Showing results 1 to 2 of 2

 

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