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Another case of holoprosencephaly associated with RAD21 loss-of-function variant.

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Bibliographic Details
Title: Another case of holoprosencephaly associated with RAD21 loss-of-function variant.
Authors: Goel H; Hunter Genetics, Waratah, NSW 2298, Australia., Parasivam G; Hunter Genetics, Waratah, NSW 2298, Australia.
Source: Brain : a journal of neurology [Brain] 2020 Aug 01; Vol. 143 (8), pp. e64.
Publication Type: Letter; Comment
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE
Database: MEDLINE Ultimate
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Description
ISSN:1460-2156
DOI:10.1093/brain/awaa173