Danielle C. Lynch
Calgary, AB, Canada
Last Updated: 09/26/2026
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Found 8 publications
Fifty years of recognizable patterns of human malformation: Insights and opportunities.
Journal: American journal of medical genetics. Part A
Published: February 03, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Journal: Nature communications
Published: October 15, 2020
Men's Mate Value Correlates with a Less Restricted Sociosexual Orientation: A Meta-Analysis.
Journal: Archives of sexual behavior
Published: September 30, 2019
Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings.
Journal: American journal of medical genetics. Part A
Published: October 27, 2015
Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome.
Journal: Nature communications
Published: February 07, 2014
Identification of novel mutations confirms PDE4D as a major gene causing acrodysostosis.
Journal: Human mutation
Published: April 16, 2012
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly.
Journal: American journal of human genetics
Published: October 27, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026