Talk:Sertoli cell-only syndrome
Latest comment: 3 years ago by Vaticidalprophet in topic "Genetic lineage"
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Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Sertoli cell-only syndrome.
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TEX101
editMore discussion and citations regarding TEX101 for NOA are at: https://clinicaltrials.gov/ct2/show/NCT02851966 — Preceding unsigned comment added by 2601:4B:1:1BEE:31A1:D68F:8675:842 (talk) 18:31, 18 March 2017 (UTC)
Thank you, added Full Decent (talk) 07:12, 13 April 2017 (UTC)
"Genetic lineage"
editI added this language:
> Ethnicity and genetic lineage may have an impact on treatment of azoospermia [citation needed].
Maybe there is a better way to phrase this. I have seen medical articles study Jewish background versus non-Jewish background and European background versus non-European background. Sorry, no references to share at this time.
Full Decent (talk) 07:14, 13 April 2017 (UTC)
- Full Decent, and it remains unsourced. I veered toward this article because it's connected to related topics I'm editing and reading about. This page is small enough that I can source the whole thing within an hour, but a quick search pulls up nothing for "Ethnicity and genetic lineage may have an impact on treatment of azoospermia" so far. I'm not going to add resources to this page today, but I'll probably come back to it and do that. GBFEE (talk) 18:43, 30 October 2021 (UTC)
- Vaticidalprophet located a resource for the line. It was already in the article.[1] Vaticidalprophet, you appear exasperated that I hadn't spotted it by briefly looking over the article. I had not yet examined the resources on the page. The line was there for years, and someone else should have already cited it. Also, do you mind revealing how you made your way to this page to help? This article gets so little edits and that was your first edit to the page. I'm interested, you know? GBFEE (talk) 19:57, 31 October 2021 (UTC)
- I hadn't read this talk page before -- my exasperation was not directed at individuals. When I was more active, I edited extensively in the fields of genetic disorders and particularly sex chromosome anomalies, several articles about which I had major enough contributions to list on my userpage. It should be fairly clear someone interested in conditions of which several cause this disorder might happen to be reading an article about it. Since tapering down my activity, most of my editing has been articles I was reading at the time and noticed easy-to-fix issues with; this pattern can be seen in my recent edits. Vaticidalprophet 21:25, 31 October 2021 (UTC)