Chromosome 17p13.1 deletion syndrome is a phenotype in humans that is designed DEL17P13.1.[1][2]
References
- ^ "Entrez Gene: Chromosome 17p13.1 deletion syndrome".
- ^ Carvalho CM, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, et al. (November 2014). "Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes". American Journal of Human Genetics. 95 (5): 565–78. doi:10.1016/j.ajhg.2014.10.006. PMC 4225592. PMID 25439725.