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5. Exon skip‐inducing variants in FLNA in an attenuated form of frontometaphyseal dysplasia. Issue 12 (17th July 2021)

7. Genomic and signalling pathway characterization of the NZM panel of melanoma cell lines: A valuable model for studying the impact of genetic diversity in melanoma. (4th July 2020)

8. Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome. Issue 3 (29th November 2019)