A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
Keskin, Melikşah ; Muratoğlu Şahin, Nursel ; Kurnaz, Erdal ; Bayramoğlu, Elvan ; Savaş Erdeve, Şenay ; Aycan, Zehra ; Çetinkaya, Semra Darendeliler,Fatma Feyza
Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.91-94 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. Ltd
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