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Publications by C S Perrotta

Duplications in Addition to Terminal Deletions Are Present in a Proportion of Ring Chromosomes: Clues to the Mechanisms of Formation

Journal of Medical Genetics

English

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De Novo Deletions and Duplications of 17q25.3 Cause Susceptibility to Cardiovascular Malformations

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Deletions of the RUNX2 Gene Are Present in About 10% of Individuals With Cleidocranial Dysplasia

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The Clues Are in the History

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Opposite Deletions/Duplications of the X Chromosome: Two Novel Reciprocal Rearrangements

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Thousands of RNA-cached Copies of Whole Chromosomes Are Present in the Ciliate Oxytricha During Development

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FISHing for Mechanisms of Cytogenetically Defined Terminal Deletions Using Chromosome-Specific Subtelomeric Probes

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