The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability
Crossref DOI link: https://doi.org/10.1186/s13039-016-0286-0
Published Online: 2016-09-29
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Ha, Kyungsoo
Shen, Yiping
Graves, Tyler
Kim, Cheol-Hee
Kim, Hyung-Goo