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Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees.
Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence.
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Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence.
Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence. medRxiv. 2020 May 13.
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authors with profiles
Vineet Arora
David Meltzer
Julian Solway
Tamara Vokes