Preview

Medical Genetics

Advanced search

Section Details


CASE REPORT

 
Issue Title
 
Vol 12, No 2 (2013) WERNER MESOMELIC SYNDROME WITH PREAXIAL POLYDACTYLY, INDUCED BY MUTATION IN ZONE OF POLARIZING ACTIVITY REGULATORY SEQUENCE (ZRS) OF GENE SHH Abstract   PDF (Rus)
V. P. Fedotov, N. M. Galeeva, A. V. Polyakov
 
Vol 19, No 11 (2020) Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability and autism spectrum disorder Abstract   PDF (Rus)
T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, N. N. Zavadenko, A. G. Prityko
 
1 - 2 of 2 Items