Items where Author is "Ronasian, F."
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Number of items: 2.
Article
(2018) A homozygous NOP14 variant is likely to cause recurrent pregnancy loss. Journal of Human Genetics. pp. 425-430. ISSN 1434-5161
(2016) A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract. Journal of Human Genetics. pp. 177-179. ISSN 1434-5161