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Publications by StefanM. Pulst

A 163-Bp Deletion at the C-Terminus of the Schwannomin Gene Associated With Variable Phenotypes of Neurofibromatosis Type 2

Human Genetics
Genetics
1995English

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Heterogeneous Phenotypes of Japanese Cases With a Growth Hormone Gene Deletion

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Calvarial Defects Associated With Neurofibromatosis Type 1

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A Small Recurrent Deletion Within 15q13.3 Is Associated With a Range of Neurodevelopmental Phenotypes

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