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SPATA16
Non-Syndromic Monogenic Male Infertility
Genetic Counseling and Diagnostic Guidelines for Couples with Infertility And/Or Recurrent Miscarriage
Genetics of Male Infertility: Genes Implicated in Non-Obstructive
Cellular and Molecular Aspects of the Response of the Testis to Nutrition In
Major Spliceosome Defects Cause Male Infertility and Are Associated with Nonobstructive Azoospermia in Humans
Genetic Evaluation of Patients with Non-Syndromic Male Infertility
Single-Cell RNA Sequencing of Human, Macaque, and Mouse Testes Uncovers Conserved and Divergent Features of Mammalian Spermatogenesis
Novel Mutations Segregating with Complete Androgen Insensitivity Syndrome and Their Molecular Characteristics
HIPK4 Is Essential for Murine Spermiogenesis
Globozoospermia Syndrome: an Update
Layout of Course Male Infertility Spermatogenic Failure
AU040320 Deficiency Leads to Disruption of Acrosome Biogenesis
Gene Disruption Causes Globozoospermia and Infertility in Male Mice
Leydig Cell Hyperplasia in an ENU-Induced Mutant Mouse With
Population-Specific, Recent Positive Directional Selection Suggests
Human Genetics of Male Infertility Elias Elinati
New Insights Into the Genetics of Spermatogenic Failure: a Review of the Literature
Exome Sequencing Reveals Novel Causes As Well As New Candidate Genes for Human Globozoospermia
Top View
Major Spliceosome Defects Cause Male Infertility and Are Associated with Nonobstructive Azoospermia in Humans
Genetic Investigation in Non-Obstructive Azoospermia: from the X Chromosome to The
Recent Advances and Future Opportunities to Diagnose Male Infertility
Teratozoospermia: Spotlight on the Main Genetic Actors in the Human
Complete Globozoospermia Associated with DPY19L2 Mutation
Understanding Fertilization Through Intracytoplasmic Sperm Injection (ICSI)ଝ
Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility
The Genetics of Human Infertility by Functional Interrogation of Snps in Mice
UC Riverside UC Riverside Previously Published Works