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Molecular and Cellular Pediatrics
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October 5, 2021
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis
Clara 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 anomalies
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 2) with videos related to
Sort By:
Page
of 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 paraparesis
Clara 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 anomalies
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
Page
of 1