Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.1007/s13258-022-01344-8
dc.identifier.other
WOS:000882351800003
dc.description.volume
dc.description.issue
Publisher
SPRINGER
DOI
10.1007/s13258-022-01344-8