Montserrat Milà (Editor)
Biochemistry and Molecular Genetics Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Dr. Mila has dedicated her research to the study of molecular and cytogenetic pathology. Her diagnostic and research has been focused on the study of the Fragile X Syndrome and the molecular basis of intellectual disability. She has been the Principal Investigator of 12 projects and has collaborated in 8 more. She has 135 papers in peer review journals and 10 book chapters.
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Allelic Forms of the FMR1 Gene: Fragile X Syndrome, Primary Ovarian Insufficiency and Tremor Ataxia Syndrome among Others
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