ArticleClinical genetics2019
Novel heterozygous variants in KMT2D associated with holoprosencephaly.
Cedrik Tekendo-Ngongang et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleClinical genetics2019
Cedrik Tekendo-Ngongang et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.