SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [PDF]
Shaw ND +77 more
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Brief von Josef Steindl an Toshio Ogata
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Steindl, Josef
core
Brief von Josef Steindl an Krishna Bharadwaj
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Steindl, Josef
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Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability. [PDF]
De Hayr L +36 more
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Brief von Josef Steindl an Manuela Mosca
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Steindl, Josef
core
Potential of ex vivo organotypic slice cultures in neuro-oncology. [PDF]
Steindl A, Valiente M.
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The AVIATOR registry: the importance of evaluating long-term patient outcomes. [PDF]
de Heer F +8 more
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A multi-center, open label, single group, observational clinical trial to investigate the effects of training on the administration of Cardioplexol™. [PDF]
Tevaearai Stahel HT +15 more
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Brief von Josef Steindl an Jerzy Osiatyński
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Steindl, Josef
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Brief von Josef Steindl an Jan Kregel
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Steindl, Josef
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