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Quoted phrase not found in phrase index: "Spermatogenic failure, Y-linked, 2"
Page 1
Spermatogenic failure and the Y chromosome.
Hum Genet. 2017 May;136(5):637-655. doi: 10.1007/s00439-017-1793-8. Epub 2017 Apr 29.
Hum Genet. 2017.
PMID: 28456834
Review.
The Y chromosome harbors a number of genes essential for testis development and function. Its highly repetitive structure predisposes this chromosome to deletion/duplication events and is responsible for Y-linked copy-number variations (CNVs) with clinical re …
The Y chromosome harbors a number of genes essential for testis development and function. Its highly repetitive structure predisposes …
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.
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Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory.
Lo Giacco D, Chianese C, Sánchez-Curbelo J, Bassas L, Ruiz P, Rajmil O, Sarquella J, Vives A, Ruiz-Castañé E, Oliva R, Ars E, Krausz C.
Lo Giacco D, et al.
Eur J Hum Genet. 2014 Jun;22(6):754-61. doi: 10.1038/ejhg.2013.253. Epub 2013 Nov 6.
Eur J Hum Genet. 2014.
PMID: 24193344
Free PMC article.
Gr/gr deletion, but not AZFc partial duplications, was significantly associated with spermatogenic impairment. Our data integrated with the literature suggest that: (1) routine AZF microdeletion testing could eventually include only men with 2 10(6)/ml; (2) c …
Gr/gr deletion, but not AZFc partial duplications, was significantly associated with spermatogenic impairment. Our data integrated wi …
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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
After investigation, we found the following karyotype: 45,X,dic(Y;22)(q11.223;p11.2). This investigation contributes to our understanding of how chromosome rearrangements can influence fertility processes and how important it is to perform a cytogenetic analysis in inferti …
After investigation, we found the following karyotype: 45,X,dic(Y;22)(q11.223;p11.2). This investigation contributes to our understan …
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First study of microdeletions in the Y chromosome of Algerian infertile men with idiopathic oligo- or azoospermia.
Chellat D, Rezgoune ML, McElreavey K, Kherouatou N, Benbouhadja S, Douadi H, Cherifa B, Abadi N, Satta D.
Chellat D, et al.
Urol Int. 2013;90(4):455-9. doi: 10.1159/000347046. Epub 2013 Mar 16.
Urol Int. 2013.
PMID: 23548818
Among the 80 infertile men screened for microdeletion, 1 subject was found to have microdeletions in the AZFc (sY254 and sY255) region. The deletion was found in azoospermic subjects (1/49, 2%). The overall AZF deletion frequency was low (1/80, 1.3%). AZF microdeletions we …
Among the 80 infertile men screened for microdeletion, 1 subject was found to have microdeletions in the AZFc (sY254 and sY255) region. The …
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