A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene
- DOI
- 10.1002/ccr3.4882
- Published
- 2021-12
- Container
- Clinical Case Reports
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/ccr3.4882,
title = {A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene},
author = {Claire Balza and Giulia Garofalo and Teresa Cos and Julie Désir and Xin Kang and Kathelijn Keymolen and Julie Soblet and Kim Van Berkel and Catheline Vilain and Wafa Ben Abbou and Marie Cassart},
year = {2021},
journal = {Clinical Case Reports},
doi = {10.1002/ccr3.4882},
url = {https://doi.org/10.1002/ccr3.4882}
}RIS
TY - JOUR TI - A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene AU - Claire Balza AU - Giulia Garofalo AU - Teresa Cos AU - Julie Désir AU - Xin Kang AU - Kathelijn Keymolen AU - Julie Soblet AU - Kim Van Berkel AU - Catheline Vilain AU - Wafa Ben Abbou AU - Marie Cassart PY - 2021 JO - Clinical Case Reports DO - 10.1002/ccr3.4882 UR - https://doi.org/10.1002/ccr3.4882 ER -
APA
Balza, C., Garofalo, G., Cos, T., Désir, J., Kang, X., Keymolen, K., Soblet, J., Berkel, K. V., Vilain, C., Abbou, W. B., & Cassart, M. (2021). A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene. Clinical Case Reports. https://doi.org/10.1002/ccr3.4882
Source records
- crossref · retrieved 2026-09-27T12:06:02.290Z