«Fascinating
genetic studies had been done on SMCHD1 that linked the gene to FSHD2, a rare muscular dystrophy involving the interaction of multiple genetic sites, but it had never been connected to craniofacial abnormalities,» says Michael Talkowski, PhD, of the MGH Center for Human Genetic Research, co-senior author of the Nature Genetics
genetic studies had been done on SMCHD1 that linked the gene to FSHD2, a
rare muscular dystrophy involving the interaction of multiple
genetic sites, but it had never been connected to craniofacial abnormalities,» says Michael Talkowski, PhD, of the MGH Center for Human Genetic Research, co-senior author of the Nature Genetics
genetic sites, but it had never been connected to craniofacial
abnormalities,» says Michael Talkowski, PhD, of the MGH Center for Human
Genetic Research, co-senior author of the Nature Genetics
Genetic Research, co-senior author of the Nature Genetics paper.