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Molecular Cytogenetics|June 1, 2010
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pairDilek Aktas, Eda G Utine, Kristin Mrasek, et al.Clinical and Experimental Immunology|May 18, 2026
CD137 deficiency patients: two new patients and review of the literatureZehra Genc Ozbay, Busra Kocali, Deniz Ilgun Gurel, et al.American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.Journal of Tissue Viability|October 23, 2021
Impact of tailored training about pressure injuries on nurses' knowledge levels and pressure injury point prevalence: The case of TurkeyZehra Gocmen Baykara, Ayise Karadag, Sevilay Senol Celik, et al.Journal of Wound, Ostomy, and Continence Nursing : Official Publication of the Wound, Ostomy and Continence Nurses Society|July 19, 2023
Pressure Injury Prevalence and Risk Factors: A National Multicenter Analytical StudyZehra Gocmen Baykara, Ayise Karadag, Hulya Bulut, et al.Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.Thrombosis and Haemostasis|December 22, 2010
Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activityJürgen Klammt, Louise Kobelt, Dilek Aktas, et al.American Journal of Human Genetics|April 6, 2010
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfectaYasemin Alanay, Hrispima Avaygan, Natalia Camacho, et al.International Journal of Molecular Medicine|May 29, 2008
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literatureMarina Manvelyan, Mariluce Riegel, Monica Santos, et al.Blood|July 20, 2006
Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patientsKatrin Tefs, Maria Gueorguieva, Jürgen Klammt, et al.Pageof 4