Sertoli Cell-only Syndrome
What's New
Last Posted: Oct 01, 2024
- A retrospective analysis of 1600 infertility patients with azoospermia and severe oligozoospermia.
Bing Yi Zhou, et al. Clinica chimica acta; international journal of clinical chemistry 2024 0 119973 - Male infertility in Sertoli cell-only syndrome: An investigation of autosomal gene defects.
Koc Gulsah, et al. International journal of urology : official journal of the Japanese Urological Association 2018 0 (2) 292-298 - Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Kasak Laura, et al. American journal of human genetics 2018 0 (2) 200-212 - Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome.
Murtaza Ghulam, et al. Genetic testing and molecular biomarkers 2021 0 (10) 654-659 - Analysis of 29 Targeted Genes for Non-Obstructive Azoospermia: The Relationship between Genetic Testing and Testicular Histology.
Cannarella Rossella, et al. The world journal of men's health 2022 0 - Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang Dongdong, et al. Reproductive biology and endocrinology : RB&E 2022 0 (1) 63 - Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia.
Zhang Yuxiang, et al. Frontiers in genetics 2022 0 799886 - Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Cerván-Martín Miriam, et al. Andrology 2022 6 - Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
Cerván-Martín Miriam, et al. Journal of personalized medicine 2022 6 (6) - Partial-AZFc deletions in Chilean men with primary spermatogenic impairment: gene dosage and Y-chromosome haplogroups.
Lardone María Cecilia, et al. Journal of assisted reproduction and genetics 2020 10
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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