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Quoted phrase not found in phrase index: "Spermatogenic failure 32"
Page 1
Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.
Dong Y, Pan Y, Wang R, Zhang Z, Xi Q, Liu RZ. Dong Y, et al. Genet Mol Res. 2015 Dec 7;14(4):16041-9. doi: 10.4238/2015.December.7.17. Genet Mol Res. 2015. PMID: 26662397 Free article.
Spermatogenic failure patients consisting of 13 males with chromosomal abnormalities and 20 with unexplained azoospermia were enrolled. ...By applying high throughput genome-wide sequencing to determine CNVs, we provide a number of candidate genes possibly contribut …
Spermatogenic failure patients consisting of 13 males with chromosomal abnormalities and 20 with unexplained azoospermia were …
A systematic review and standardized clinical validity assessment of male infertility genes.
Oud MS, Volozonoka L, Smits RM, Vissers LELM, Ramos L, Veltman JA. Oud MS, et al. Hum Reprod. 2019 May 1;34(5):932-941. doi: 10.1093/humrep/dez022. Hum Reprod. 2019. PMID: 30865283 Free PMC article.
The clinical validity of these gene-disease relationships varied widely and ranged from definitive (n = 38) to strong (n = 22), moderate (n = 32), limited (n = 93) or no evidence (n = 160). A total of 176 gene-disease relationships could not be classified because our scori …
The clinical validity of these gene-disease relationships varied widely and ranged from definitive (n = 38) to strong (n = 22), moderate (n …
AZF deletions in Indian populations: original study and meta-analyses.
Waseem AS, Singh V, Makker GC, Trivedi S, Mishra G, Singh K, Rajender S. Waseem AS, et al. J Assist Reprod Genet. 2020 Feb;37(2):459-469. doi: 10.1007/s10815-019-01661-0. Epub 2020 Jan 9. J Assist Reprod Genet. 2020. PMID: 31919744 Free PMC article.
Qualitative analysis showed that AZF deletions were present in 0.59 to 32.62% (average 13.48%) of infertile cases in Indian populations. ...Pooled analysis for all studies showed deletion frequency from 0.59 to 32.62% (average = 13.48%). Meta-analysis showed signifi …
Qualitative analysis showed that AZF deletions were present in 0.59 to 32.62% (average 13.48%) of infertile cases in Indian populatio …
45,X karyotype in an infertile man: how is this possible?
Amaro A, Mafra FA, Valada Pane CE, Kulikowski LD, Bianco B, Barbosa CP, Christofolini DM. Amaro A, et al. Urol Int. 2015;94(4):488-90. doi: 10.1159/000365010. Epub 2014 Aug 20. Urol Int. 2015. PMID: 25170625
The case was male, 32 years old, with a nonobstructive azoospermia diagnosis and an initial 45,X karyotype. ...
The case was male, 32 years old, with a nonobstructive azoospermia diagnosis and an initial 45,X karyotype. ...
Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
Castro A, Rodríguez F, Flórez M, López P, Curotto B, Martínez D, Maturana A, Lardone MC, Palma C, Mericq V, Ebensperger M, Cassorla F. Castro A, et al. Hum Reprod. 2017 Feb;32(2):465-475. doi: 10.1093/humrep/dew333. Epub 2017 Jan 5. Hum Reprod. 2017. PMID: 28057878
WHAT IS KNOWN ALREADY: The microdeletions in the long arm of the Y chromosome (Yq) that include the loss of one to three AZF regions, referred to as Yq microdeletions, constitute the most important known etiological factor for primary spermatogenic failure. Recently …
WHAT IS KNOWN ALREADY: The microdeletions in the long arm of the Y chromosome (Yq) that include the loss of one to three AZF regions, referr …
Frequency of microdeletions in the azoospermia factor region of the Y-chromosome of New Zealand men.
Kerr NJ, Zhang J, Sin FY, Benny P, Sin IL. Kerr NJ, et al. N Z Med J. 2000 Nov 10;113(1121):468-70. N Z Med J. 2000. PMID: 11194754
Azoospermic men have a higher frequency of microdeletions than men with less severe spermatogenic failure. Men with microdeletions can have reduced fertility, but are not necessarily sterile....
Azoospermic men have a higher frequency of microdeletions than men with less severe spermatogenic failure. Men with microdelet …