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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 23, 2020
Airway Morphological Changes in Pierre Robin Sequence: A Retrospective StudyLaura S Humphries, Tulsi Roy, Anne Huang, et al.
Plastic and Reconstructive Surgery. Global Open|February 22, 2018
SSET Project: Cost-effectiveness Analysis of Surgical Specialty Emergency Trays in the Emergency DepartmentLaura S Humphries, Deana S Shenaq, Chad M Teven, et al.
Human Genetics|January 1, 1989
The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6G Lindahl, E Gersdorf, H J Menzel, et al.
Clinical Genetics|July 1, 1991
Identification of the 664 proline to leucine mutation in the low density lipoprotein receptor in four unrelated patients with familial hypercholesterolaemia in the UKL King-Underwood, V Gudnason, S Humphries, et al.
Arteriosclerosis (Dallas, Tex.)|July 1, 1990
Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in MunichH Schuster, G Rauh, B Kormann, et al.
The Journal of Clinical Investigation|November 1, 1988
Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemiaP J Talmud, J K Lloyd, D P Muller, et al.
Arteriosclerosis (Dallas, Tex.)|January 1, 1989
Gene probes in diagnosis of familial hypercholesterolemiaS Humphries, R Taylor, M Jeenah, et al.
European Journal of Clinical Investigation|March 27, 1999
Cholesteryl ester transfer protein gene effect on CETP activity and plasma high-density lipoprotein in European populations. The EARS GroupV Gudnason, S Kakko, V Nicaud, et al.
Human Genetics|May 17, 2001
Elite swimmers and the D allele of the ACE I/D polymorphismD Woods, M Hickman, Y Jamshidi, et al.
Atherosclerosis|August 1, 1991
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaP Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.
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