Desmond A. Brown, Ph.D. - Publications
Affiliations: | 2012 | Molecular Biology | Princeton University, Princeton, NJ |
Area:
Molecular Biology, Human Development, Neuroscience BiologyYear | Citation | Score | |||
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2010 | Walczak-Sztulpa J, Eggenschwiler J, Osborn D, Brown DA, Emma F, Klingenberg C, Hennekam RC, Torre G, Garshasbi M, Tzschach A, Szczepanska M, Krawczynski M, Zachwieja J, Zwolinska D, Beales PL, et al. Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. American Journal of Human Genetics. 86: 949-56. PMID 20493458 DOI: 10.1016/J.Ajhg.2010.04.012 | 0.561 | |||
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