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Lymphology|July 27, 2022
A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?P S Buonuomo, M El Hachem, G Mastrogiorgio, et al.European Journal of Medical Genetics|November 11, 2021
Congenital heart defects in the recurrent 2q13 deletion syndromeM C Digilio, M L Dentici, S Loddo, et al.Clinical Genetics|December 6, 2012
Syndromic non-compaction of the left ventricle: associated chromosomal anomaliesM C Digilio, L Bernardini, M G Gagliardi, et al.Clinical Genetics|October 2, 2009
Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints locationC Surace, S Piazzolla, P Sirleto, et al.Pageof 2