G. Gentile

TRISOMY-18 SYNDROME DUE TO DE-NOVO TRANSLOCATION

F. Hecht, E. Kaplan, J. Bryant, 1963 .

Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome

M. Kinali, V. Salpietro, K. McElreavey, 2015, Journal Genetika.

Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome

M. Kinali, V. Salpietro, K. McElreavey, 2015, Journal of Genetics.