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Publications by Joan E. Pellegrino

Myoclonus-Dystonia Syndrome Associated With Russell Silver Syndrome

Movement Disorders
Neurology
2013English

Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child With Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes

JIMD Reports
Internal MedicineGeneticsMolecular BiologyBiochemistryEndocrinologyMetabolismDiabetes
2014English

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