Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report.
- DOI
- 10.1186/s12920-018-0471-6
- Published
- 2019 Jan 10
- Container
- BMC medical genomics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s12920-018-0471-6,
title = {Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report.},
author = {Danyel M and Suk EK and Raile V and Gellermann J and Knaus A and Horn D},
year = {2019},
journal = {BMC medical genomics},
doi = {10.1186/s12920-018-0471-6},
url = {https://doi.org/10.1186/s12920-018-0471-6}
}RIS
TY - JOUR TI - Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report. AU - Danyel M AU - Suk EK AU - Raile V AU - Gellermann J AU - Knaus A AU - Horn D PY - 2019 JO - BMC medical genomics DO - 10.1186/s12920-018-0471-6 UR - https://doi.org/10.1186/s12920-018-0471-6 ER -
APA
M, D., EK, S., V, R., J, G., A, K., & D, H. (2019). Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report.. BMC medical genomics. https://doi.org/10.1186/s12920-018-0471-6
Source records
- pubmed · retrieved 2026-09-25T15:24:04.196Z