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Keyword [Perrault syndrome]
Result: 1 - 4 | Page: 1 of 1
1.
The Role Of C10ORF2 And HELQ,PR1M1 Genes Played In Primary Ovarian Insufficiency
2.
Study On Pathogenic Mechanism Of Perrault Syndrome With Deafness As Clinical Manifestation Caused By HARS2 Gene Mutation
3.
Clinical And Genetic Analysis Of Rare Syndromic Hearing Loss
4.
Correlation Analysis Of Deafness Gene Detection And Curative Effect In 43 Cochlear Implant Patients And Deafness Family Study
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