2021
DOI: 10.1002/ccr3.4882
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Abstract: Reelinopathies cause a distinctive lissencephaly type associated with cerebellar hypoplasia. To help further management, we wanted to report here the first prenatal diagnosis due to a homozygous inherited reelinopathy.

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Cited by 3 publications
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“…In the article entitled “A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene,” which was previously published in Volume 9 Issue 12 of Clinical Case Reports, the statement regarding the shared first authorship was missed out in the original publication 1 . Both Claire Balza and Giulia Garofalo share the first authorship for this article.…”
mentioning
confidence: 99%
“…In the article entitled “A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene,” which was previously published in Volume 9 Issue 12 of Clinical Case Reports, the statement regarding the shared first authorship was missed out in the original publication 1 . Both Claire Balza and Giulia Garofalo share the first authorship for this article.…”
mentioning
confidence: 99%