Häfliger, I.M.
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13

A homozygous missense variant in laminin subunit beta 1 as ..:

Jacinto J. G. P ; Hafliger I. M ; Bernardini M...
info:eu-repo/semantics/altIdentifier/wos/WOS:000720318500001.  , 2021
 
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14

CNGB3 Missense Variant Causes Recessive Achromatopsia in Or..:

Häfliger, I.M ; Marchionatti, E ; Stengård, M...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms222212440.  , 2021
 
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