Publications

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Author Title [ Year(Desc)]
Filters: Author is Ng, Bobby G and Keyword is Phenotype  [Clear All Filters]
2015
Ng, B. G. et al. Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Hum Mutat 36, 1048-51 (2015).
2016
Wheeler, P. G. et al. SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. Am J Med Genet A 170, 3165-3171 (2016).