Azoospermia and paternal autosomal ring chromosomes: case report and literature review.
暂无分享,去创建一个
[1] B. Dallapiccola,et al. Azoospermia in a man with a constitutional ring 22 chromosome. , 2010, European journal of medical genetics.
[2] Y. Juliano,et al. Ring chromosome instability evaluation in six patients with autosomal rings. , 2010, Genetics and molecular research : GMR.
[3] V. Jobanputra,et al. Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling , 2009, American journal of medical genetics. Part A.
[4] F. Vialard,et al. Sperm chromosome analysis of an infertile patient with a 95% mosaic r(21) karyotype and normal phenotype. , 2009, Fertility and sterility.
[5] P. Serhal,et al. Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier , 2009, Molecular Cytogenetics.
[6] H. Taylor,et al. Ring chromosome 12 and severe oligospermia: a case report. , 2008, Fertility and Sterility.
[7] G. Gimelli,et al. Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability , 1993, Human Genetics.
[8] E. Hook,et al. Inherited ring chromosomes: an analysis of published cases , 1991, Human Genetics.
[9] G. Kosztolányi. Does “ring syndrome” exist? An analysis of 207 case reports on patients with a ring autosome , 1987, Human Genetics.
[10] B. Dallapiccola,et al. Ring chromosome 21 in healthy persons: different consequencies in females and in males , 1986, Human Genetics.
[11] C. Stoll,et al. Segregation of a 22 ring chromosome in three generations , 2004, Human Genetics.
[12] M. Speevak,et al. Molecular characterization of an inherited ring (19) demonstrating ring opening , 2003, American journal of medical genetics. Part A.
[13] A. Chandley. Chromosome anomalies and Y chromosome microdeletions as causal factors in male infertility. , 1998, Human reproduction.
[14] L. Krey,et al. The embryo versus endometrium controversy revisited as it relates to predicting pregnancy outcome in in-vitro fertilization-embryo transfer cycles. , 1997, Human reproduction.
[15] E. Engel,et al. [Prenatal diagnosis of 3 cases of ring G chromosomes: one 21 and two 22, one of which was de novo]. , 1986, Annales de genetique.
[16] J. Huret,et al. Ring chromosome 21 in a phenotypically normal but infertile man , 1985, Clinical genetics.
[17] M. Teyssier,et al. Ring chromosome 15: Report of a case in an infertile man , 1982, Clinical genetics.
[18] T. Reed,et al. Four new cases of ring 21 and 22 including familial transmission of ring 21. , 1977, Journal of medical genetics.
[19] L. Margineanu,et al. [A familial case of 17 r ring-shaped chromosome of group E with transmission from father to son]. , 1973, Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi.
[20] F. Hecht,et al. Chromosome anomalies. , 1967, Lancet.
[21] W. Brown,et al. CHROMOSOME STUDIES ON TESTICULAR CELLS FROM 50 SUBFERTILE MEN , 1966 .
[22] J. E. Newsam,et al. Studies on human meiotic chromosomes from testicular tissue. , 1966, Lancet.