(Q50310730)
Statements
A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1. (English)
1 reference
Reiner Siebert
1 reference
Inga Mohrmann
1 reference
Gabriele Gillessen-Kaesbach
1 reference
Almuth Caliebe
1 reference
Yorck Hellenbroich
1 reference
29 April 2011
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54
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4
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e461-4
1 reference