Leiden University Scholarly Publications

Persistent URL of this record https://hdl.handle.net/1887/97398

Beta release

Statistics of Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus
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202400
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2024-0800
2024-0900
2024-1000