Publication | Closed Access
Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure
12
Citations
11
References
2018
Year
InfertilityMendelian DisorderGenetic DisorderGeneticsWhole Exome SequencingMolecular GeneticsConsanguineous Turkish FamilyDisease Gene IdentificationSystems BiologyMedicineSpermatogenic Failure
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