196 research outputs found
Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene
Ectopia lentis et pupillae syndrome in three generations
Contains fulltext :
21868.PDF (publisher's version ) (Open Access
2011 report on the drugs situation in Europe.
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24314.PDF (publisher's version ) (Open Access
Anomaloscope examination: scotopization (the luminance fall)
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Gyrate atrophy and choroidal neovascularization
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23966.PDF (publisher's version ) (Open Access
Cornea-anesthesie bij kinderen met multipele congenitale afwijkingen (vertebral, anal, cardiovascular, tracheo-esophageal, renal and limb defects of VACTERL-associatie)
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25517___.PDF (publisher's version ) (Open Access
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