A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. [electronic resource]
Producer: 20180504Description: 998-1006 p. digitalISSN:- 1530-0366
- Amino Acid Sequence
- Azoospermia -- diagnosis
- Biomarkers
- Biopsy
- Case-Control Studies
- Consanguinity
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Dyneins -- genetics
- Family
- Genetic Association Studies
- Genetic Predisposition to Disease
- Genetic Testing
- Genotype
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Mutation
- Pedigree
- Spermatozoa -- metabolism
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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