T. Blaine Crowley
0000-0002-3272-5458
4 papers found
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Expanding Genetic Counselor Roles: A Model for Global Research Development
Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition
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