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Hennie Voshart-van Heeren
Hennie Voshart-van Heeren
Chromosome
Uniparental disomy
Genetics
Gene duplication
Point mutation
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Deletion atChromosome16pI3.3as a CauseofRubinstein- TaybiSyndrome: Clinical Aspects
1993
Marcel Tilanus
Hennie Voshart-van Heeren
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