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Clinical Epigenetics|January 7, 2021
DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndromeL C Schenkel, E Aref-Eshghi, K Rooney, et al.Tissue Antigens|January 1, 1996
Large-scale DRB and DQB1 oligonucleotide typing for the NMDP registry: progress report from year 2J Ng, C K Hurley, C Carter, et al.Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.Molecular Therapy. Methods & Clinical Development|November 25, 2021
Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx miceShelby E Hamm, Daniel D Fathalikhani, Katherine E Bukovec, et al.Molecular Therapy. Methods & Clinical Development|April 14, 2021
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx miceShelby E Hamm, Daniel D Fathalikhani, Katherine E Bukovec, et al.Bone Marrow Transplantation|March 30, 2010
An update to HLA nomenclature, 2010S G E Marsh, E D Albert, W F Bodmer, et al.Molecular Psychiatry|April 17, 2013
Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalitiesJ C Hodge, E Mitchell, V Pillalamarri, et al.Pageof 41