(Q51911636)
Statements
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome. (English)
1 reference
Isabel Filges
1 reference
Benno Röthlisberger
1 reference
Nemya Boesch
1 reference
Peter Weber
1 reference
Friedel Wenzel
1 reference
Andreas R Huber
1 reference
Karl Heinimann
1 reference
Peter Miny
1 reference
1 April 2010
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152A
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4
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987-993
1 reference