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Journal of Medical Genetics|June 1, 1992
No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palateG M Vintiner, S E Holder, R M Winter, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 23, 2002
Changes in high molecular weight kininogen levels during and after cardiopulmonary bypass surgery measured using a chromogenic peptide substrate assayM J Gallimore, D W Jones, M Winter, et al.
Physical Review Letters|March 16, 2018
Probing α-RuCl_{3} Beyond Magnetic Order: Effects of Temperature and Magnetic FieldStephen M Winter, Kira Riedl, David Kaib, et al.
European Journal of Psychotraumatology|November 18, 2025
Effectiveness of early psychotherapeutic interventions for trauma-exposed children and adolescents: insights from a trauma outpatient clinicElise Rohde, Lea Bentz, Romina Hübler, et al.
Frontiers in Oncology|February 27, 2019
Corrigendum: Metabolic Dependencies in Pancreatic CancerAli Vaziri-Gohar, Mahsa Zarei, Jonathan R Brody, et al.
Nature|September 28, 1989
A nuclear DNA attachment element mediates elevated and position-independent gene activityA Stief, D M Winter, W H Strätling, et al.
Journal of Medical Genetics|October 1, 1987
Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritanceK D MacDermot, S C Roth, C Hall, et al.
Drugs & Aging|December 15, 2025
Therapeutic Management of Glucocorticoid-Induced Osteoporosis with a Focus on Older Adults: A Narrative ReviewElena Tsourdi, Ulrike Baschant, Martina Rauner, et al.
European Journal of Cardiovascular Nursing|February 12, 2024
Beyond validation: getting wearable activity trackers into cardiovascular care-a discussion paperNicola Straiton, Philip Moons, Axel Verstrael, et al.
Clinical Dysmorphology|January 29, 2000
Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?A S Plomp, M Baraitser, S F Slaney, et al.
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