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Clara Vidic

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Molecular and Cellular Pediatrics|October 5, 2021
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesisClara Vidic, Marcin Zaniew, Szymon Jurga, et al.
Journal of Medical Genetics|December 23, 2024
<i>TFAP2E</i> is implicated in central nervous system, orofacial and maxillofacial anomaliesJeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
Molecular and Cellular Pediatrics|October 5, 2021
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesisClara Vidic, Marcin Zaniew, Szymon Jurga, et al.
Journal of Medical Genetics|December 23, 2024
<i>TFAP2E</i> is implicated in central nervous system, orofacial and maxillofacial anomaliesJeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
Pageof 1