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.
9. Genetic anomalies in patients with severe oligozoospermia and azoospermia in eastern Turkey: a prospective study. Ceylan GG; Ceylan C; Elyas H Genet Mol Res; 2009 Aug; 8(3):915-22. PubMed ID: 19731213 [TBL] [Abstract][Full Text] [Related]
10. Primary male infertility in Kuwait: a cytogenetic and molecular study of 289 infertile Kuwaiti patients. Mohammed F; Al-Yatama F; Al-Bader M; Tayel SM; Gouda S; Naguib KK Andrologia; 2007 Jun; 39(3):87-92. PubMed ID: 17683468 [TBL] [Abstract][Full Text] [Related]
11. Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Thai men with oligozoospermia and azoospermia. Vutyavanich T; Piromlertamorn W; Sirirungsi W; Sirisukkasem S Asian J Androl; 2007 Jan; 9(1):68-75. PubMed ID: 17187159 [TBL] [Abstract][Full Text] [Related]
12. [2 new cases of Y-autosome translocation associated with azoospermia]. Gregori-Romero M; López-Ginés C; Gil R; Galán Sánchez F; Pellín-Pérez A Rev Clin Esp; 1990 Jun; 187(2):71-3. PubMed ID: 2244061 [TBL] [Abstract][Full Text] [Related]
13. Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia. Faure AK; Aknin-Seifer I; Satre V; Amblard F; Devillard F; Hennebicq S; Chouteau J; Bergues U; Levy R; Rousseaux S Hum Reprod; 2007 Jul; 22(7):1854-60. PubMed ID: 17582144 [TBL] [Abstract][Full Text] [Related]
14. [Role of karyotype in studying male infertility]. Jalbert P; Servoz-Gavin M; Amblard F; Pison H; Augusseau S; Jalbert H; Sele B J Gynecol Obstet Biol Reprod (Paris); 1989; 18(6):724-8. PubMed ID: 2600375 [TBL] [Abstract][Full Text] [Related]
15. Impaired recognition memory in male mice with a supernumerary X chromosome. Lewejohann L; Damm OS; Luetjens CM; Hämäläinen T; Simoni M; Nieschlag E; Gromoll J; Wistuba J Physiol Behav; 2009 Jan; 96(1):23-9. PubMed ID: 18768146 [TBL] [Abstract][Full Text] [Related]
16. Genetic screening of karyotypes and azoospermic factors for infertile men who are candidates for ICSI. Chen SU; Lien YR; Ko TM; Ho HN; Yang YS; Chang HC Arch Androl; 2003; 49(6):423-7. PubMed ID: 14619941 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Segregation of chromosomes in sperm of a t(X;18)(q11;p11.1) carrier inherited from his mother: case report. Perrin A; Douet-Guilbert N; Le Bris MJ; Keromnes G; Langlois ML; Barrière P; Amice J; Amice V; De Braekeleer M; Morel F Hum Reprod; 2008 Jan; 23(1):227-30. PubMed ID: 17986483 [TBL] [Abstract][Full Text] [Related]
19. Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report. Brisset S; Izard V; Misrahi M; Aboura A; Madoux S; Ferlicot S; Schoevaert D; Soufir JC; Frydman R; Tachdjian G Hum Reprod; 2005 Aug; 20(8):2168-72. PubMed ID: 15845593 [TBL] [Abstract][Full Text] [Related]
20. [The most frequent chromosomal abnormalities in karyotypes of patients with reproductive problems]. Tavokina LV; Baronova EV; Sopko NI Tsitol Genet; 2007; 41(4):48-55. PubMed ID: 18030726 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]