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Haemophilia : the Official Journal of the World Federation of Hemophilia|January 7, 2010
Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophiliaK Kavakli, O Cogulu, S Aydogdu, et al.Molecular Genetics and Metabolism Reports|March 22, 2021
Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel <i>NAGLU</i> gene mutationsF Ozkinay, D A Emecen, M Kose, et al.Genomics|March 8, 2000
Two genes are responsible for Griscelli syndrome at the same 15q21 locusE Pastural, F Ersoy, N Yalman, et al.Journal De Mycologie Medicale|January 22, 2022
Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphaloceleS Yildirim Arslan, Z Sahbudak Bal, G Guner Ozenen, et al.Prenatal Diagnosis|September 5, 2002
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish familiesS Savas, S Eraslan, S Kantarci, et al.Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.Pageof 6