These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
422 related articles for article (PubMed ID: 24008148)
1. Y-chromosome microdeletions are not associated with SHOX haploinsufficiency. Chianese C; Lo Giacco D; Tüttelmann F; Ferlin A; Ntostis P; Vinci S; Balercia G; Ars E; Ruiz-Castañé E; Giglio S; Forti G; Kliesch S; Krausz C Hum Reprod; 2013 Nov; 28(11):3155-60. PubMed ID: 24008148 [TBL] [Abstract][Full Text] [Related]
2. 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 Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878 [TBL] [Abstract][Full Text] [Related]
3. Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions. Jorgez CJ; Weedin JW; Sahin A; Tannour-Louet M; Han S; Bournat JC; Mielnik A; Cheung SW; Nangia AK; Schlegel PN; Lipshultz LI; Lamb DJ J Clin Endocrinol Metab; 2011 Apr; 96(4):E674-9. PubMed ID: 21252244 [TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular characterization of Y microdeletions and X-linked CNV67 implications in male fertility: a 20-year experience. Pinho A; Barros A; Fernandes S Andrology; 2020 Mar; 8(2):307-314. PubMed ID: 31355535 [TBL] [Abstract][Full Text] [Related]
5. [Genetics and male infertility]. Stouffs K; Vandermaelen D; Tournaye H; Liebaers I; Van Steirteghem A; Lissens W Verh K Acad Geneeskd Belg; 2009; 71(3):115-39. PubMed ID: 20088251 [TBL] [Abstract][Full Text] [Related]
6. 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; 506(1):248-52. PubMed ID: 22750321 [TBL] [Abstract][Full Text] [Related]
7. Screening for Y-chromosome microdeletions in infertile Indian males: utility of simplified multiplex PCR. Mitra A; Dada R; Kumar R; Gupta NP; Kucheria K; Gupta SK Indian J Med Res; 2008 Feb; 127(2):124-32. PubMed ID: 18403789 [TBL] [Abstract][Full Text] [Related]
9. 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 Urol Int; 2013; 90(4):455-9. PubMed ID: 23548818 [TBL] [Abstract][Full Text] [Related]
10. Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. Kent-First M; Muallem A; Shultz J; Pryor J; Roberts K; Nolten W; Meisner L; Chandley A; Gouchy G; Jorgensen L; Havighurst T; Grosch J Mol Reprod Dev; 1999 May; 53(1):27-41. PubMed ID: 10230814 [TBL] [Abstract][Full Text] [Related]
12. Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects. Cancemi D; Iannuzzi A; Perucatti A; Montano L; Capozzi O; Spampanato C; Ventruto ML; Urciuoli M; Iannuzzi L; Ventruto V J Appl Genet; 2017 Nov; 58(4):481-486. PubMed ID: 29019057 [TBL] [Abstract][Full Text] [Related]
13. Genetic aspects of human male infertility: the frequency of chromosomal abnormalities and Y chromosome microdeletions in severe male factor infertility. Vicdan A; Vicdan K; Günalp S; Kence A; Akarsu C; Işik AZ; Sözen E Eur J Obstet Gynecol Reprod Biol; 2004 Nov; 117(1):49-54. PubMed ID: 15474244 [TBL] [Abstract][Full Text] [Related]
14. Y chromosome microdeletions in Tunisian infertile males. Rejeb I; M'rad R; Maazoul F; Trabelsi M; Ben Jemaa L; Chaabouni M; Zhioua F; Chaabouni H Pathol Biol (Paris); 2008 May; 56(3):111-5. PubMed ID: 18031951 [TBL] [Abstract][Full Text] [Related]
15. Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation. Ogata T; Wakui K; Kosho T; Muroya K; Yamanouchi Y; Takano T; Fukushima Y; Rappold G; Suzuki Y Am J Med Genet; 2000 Jun; 92(4):256-9. PubMed ID: 10842291 [TBL] [Abstract][Full Text] [Related]
16. Cytogenetic and molecular analysis of male infertility: Y chromosome deletion during nonobstructive azoospermia and severe oligozoospermia. Dada R; Gupta NP; Kucheria K Cell Biochem Biophys; 2006; 44(1):171-7. PubMed ID: 16456245 [TBL] [Abstract][Full Text] [Related]
17. Fold-change correction values for testicular somatic transcripts in gene expression studies of human spermatogenesis. Cappallo-Obermann H; Feig C; Schulze W; Spiess AN Hum Reprod; 2013 Mar; 28(3):590-8. PubMed ID: 23303554 [TBL] [Abstract][Full Text] [Related]
18. Screening for Y chromosome microdeletions in idiopathic and nonidiopathic infertile men with varicocele and cryptorchidism. Song NH; Wu HF; Zhang W; Zhuo ZM; Qian LX; Hua LX; Guo L; Feng NH Chin Med J (Engl); 2005 Sep; 118(17):1462-7. PubMed ID: 16157049 [TBL] [Abstract][Full Text] [Related]
19. Assisted reproductive technology may increase clinical mutation detection in male offspring. Feng C; Wang LQ; Dong MY; Huang HF Fertil Steril; 2008 Jul; 90(1):92-6. PubMed ID: 18258231 [TBL] [Abstract][Full Text] [Related]
20. Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer. Benito-Sanz S; Royo JL; Barroso E; Paumard-Hernández B; Barreda-Bonis AC; Liu P; Gracía R; Lupski JR; Campos-Barros Á; Gómez-Skarmeta JL; Heath KE J Med Genet; 2012 Jul; 49(7):442-50. PubMed ID: 22791839 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]