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Publications by D. Heron

MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2018English

Molecular Analysis of Pericentrin Gene (PCNT) in a Series of 24 Seckel/Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II) Families

Journal of Medical Genetics
Genetics
2009English

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