Results 31 to 40 of about 50 (48)
Some of the next articles are maybe not open access.

EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions

Pediatric Nephrology, 2006
Rika Fujimaru   +2 more
exaly  

Hybrid FEM-DDM and BEM-BoR for the Analysis of Multiscale Composite Structures

IEEE Transactions on Antennas and Propagation, 2020
Ping-Hao Jia   +2 more
exaly  

Accurate ab initio calculations of spectroscopic constants and properties of BeLi+

Journal of Molecular Spectroscopy, 2018
Renu Bala   +2 more
exaly  

‘New’ manifestations of BOR syndrome

Clinical Genetics, 1999
Boris G Kousseff
exaly  

Identification of a novel mutation in the EYA1 gene in a Korean family with branchio-oto-renal (BOR) syndrome

International Journal of Pediatric Otorhinolaryngology, 2005
Chang-Seok Ki, Jong-Won Kim
exaly  

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