DEL17P13.1
Protein-coding gene in humans
Chromosome 17p13.1 deletion syndrome
is a
phenotype
in humans that is designed DEL17P13.1.
[
1
]
[
2
]
^
"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
.