Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
Successful second delivery outcome using refrozen thawed testicular sperm from an infertile male true hermaphrodite with a 46, XX/46, XY karyotype: case report.
Sugawara N, Kimura Y, Araki Y.
Hum Cell. 2012 Dec;25(4):96-9. doi: 10.1007/s13577-012-0054-3. Epub 2012 Dec 1.
Related citations
Characterization of the first adult de novo case of 46,X,der(Y)t(X;Y)(p22.3;q11.2).
Bukvic N, Cesarano C, Ceccarini C, Bruno M, Lipsi MR, Gallicchio MG, Carboni MA, Valente L, Cotoia G, Antonetti R.
Gene. 2013 Jan 15;513(1):111-7. doi: 10.1016/j.gene.2012.09.133. Epub 2012 Nov 1.
AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.
Rozen SG, Marszalek JD, Irenze K, Skaletsky H, Brown LG, Oates RD, Silber SJ, Ardlie K, Page DC.
Am J Hum Genet. 2012 Nov 2;91(5):890-6. doi: 10.1016/j.ajhg.2012.09.003. Epub 2012 Oct 25.
45,X/46,XY qh- karyotype and aspermia. A case report.
Mendeluk GR, Pardes EM, López-Costa S.
Tsitol Genet. 2012 Jul-Aug;46(4):27-30.
Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients.
Mokánszki A, Molnár Z, Ujfalusi A, Balogh E, Bazsáné ZK, Varga A, Jakab A, Oláh É.
Reprod Biomed Online. 2012 Dec;25(6):620-6. doi: 10.1016/j.rbmo.2012.08.003. Epub 2012 Sep 10.
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.
Krausz C, Giachini C, Lo Giacco D, Daguin F, Chianese C, Ars E, Ruiz-Castane E, Forti G, Rossi E.
PLoS One. 2012;7(10):e44887. doi: 10.1371/journal.pone.0044887. Epub 2012 Oct 9.
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.
Yakut S, Cetin Z, Clark OA, Usta MF, Berker S, Luleci G.
Gene. 2013 Jan 1;512(1):157-60. doi: 10.1016/j.gene.2012.09.063. Epub 2012 Sep 29.
Human Y chromosome microdeletion analysis by PCR multiplex protocols identifying only clinically relevant AZF microdeletions.
Vogt PH, Bender U.
Methods Mol Biol. 2013;927:187-204.
The tricky path to recombining X and Y chromosomes in meiosis.
Kauppi L, Jasin M, Keeney S.
Ann N Y Acad Sci. 2012 Sep;1267:18-23. doi: 10.1111/j.1749-6632.2012.06593.x. Review.
Impaired spermatogenesis and gr/gr deletions related to Y chromosome haplogroups in Korean men.
Choi J, Song SH, Bak CW, Sung SR, Yoon TK, Lee DR, Shim SH.
PLoS One. 2012;7(8):e43550. doi: 10.1371/journal.pone.0043550. Epub 2012 Aug 23.
Acrocentric bivalents positioned preferentially nearby to the XY pair in metaphase I human spermatocytes.
Sarrate Z, Blanco J, Vidal F.
Fertil Steril. 2012 Nov;98(5):1241-5. doi: 10.1016/j.fertnstert.2012.07.1110. Epub 2012 Aug 9.
Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogram.
Kumari A, Yadav SK, Ali S.
PLoS One. 2012;7(7):e41488. doi: 10.1371/journal.pone.0041488. Epub 2012 Jul 23.
Sperm counts and sperm sex ratio in male infertility patients.
Eisenberg ML, Murthy L, Hwang K, Lamb DJ, Lipshultz LI.
Asian J Androl. 2012 Sep;14(5):683-6. doi: 10.1038/aja.2012.58. Epub 2012 Jul 30.
Deletion or underexpression of the Y-chromosome genes CDY2 and HSFY is associated with maturation arrest in American men with nonobstructive azoospermia.
Stahl PJ, Mielnik AN, Barbieri CE, Schlegel PN, Paduch DA.
Asian J Androl. 2012 Sep;14(5):676-82. doi: 10.1038/aja.2012.55. Epub 2012 Jul 23.
A preliminary study of the relationship between the long arm of the Y chromosome (Yqh+) and reproductive outcomes in IVF/ICSI-ET.
Xiao Z, Zhou X, Xu W, Yang J.
Eur J Obstet Gynecol Reprod Biol. 2012 Nov;165(1):57-60. doi: 10.1016/j.ejogrb.2012.07.004. Epub 2012 Jul 21.
Chromosomal aberrations, Yq microdeletion, and sperm DNA fragmentation in infertile men opting for assisted reproduction.
Shamsi MB, Kumar R, Malhotra N, Singh N, Mittal S, Upadhyay AD, Dada R.
Mol Reprod Dev. 2012 Sep;79(9):637-50. doi: 10.1002/mrd.22072. Epub 2012 Jul 31.
A single-nucleotide polymorphism of the DAZL gene promoter confers susceptibility to spermatogenic failure in the Taiwanese Han.
Teng YN, Chang YP, Tseng JT, Kuo PH, Lee IW, Lee MS, Kuo PL.
Hum Reprod. 2012 Sep;27(9):2857-65. doi: 10.1093/humrep/des227. Epub 2012 Jun 29.
Genome-wide screening of severe male factor infertile patients using BAC-array comparative genomic hybridization (CGH).
Song SH, Shim SH, Bang JK, Park JE, Sung SR, Cha DH.
Gene. 2012 Sep 10;506(1):248-52. doi: 10.1016/j.gene.2012.06.030. Epub 2012 Jun 28.
Discrepancy in the frequency of Y chromosome microdeletions among Iranian infertile men with azoospermia and severe oligozoospermia.
Saliminejad K, Sadeghi MR, Kamali K, Amirjannati N, Soltanghoraee H, Khorram Khorshid HR.
Genet Test Mol Biomarkers. 2012 Aug;16(8):931-4. doi: 10.1089/gtmb.2011.0378. Epub 2012 Jun 29.
Partial microdeletions in the Y-chromosome AZFc region are not a significant risk factor for spermatogenic impairment in Tunisian infertile men.
Ghorbel M, Gargouri SB, Zribi N, Abdallah FB, Cherif M, Keskes R, Chakroun N, Sellami A, McElreavey K, Fakhfakh F, Ammar-Keskes L.
Genet Test Mol Biomarkers. 2012 Jul;16(7):775-9. doi: 10.1089/gtmb.2012.0024. Epub 2012 Jun 25.
Filters: Manage Filters