Items where authors include "Miller, D.T."
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Number of items: 2.
Article
Zarate, Y.A., Bosanko, K.A., Thomas, M.A. et al. (18 more authors) (2021) Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Clinical Genetics, 99 (4). pp. 547-557. ISSN 0009-9163
Koczkowska, M., Chen, Y., Callens, T. et al. (72 more authors) (2018) Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848. American Journal of Human Genetics, 102 (1). pp. 69-87. ISSN 0002-9297