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214 related items for PubMed ID: 3180846
1. Meiotic analysis of two human reciprocal X-autosome translocations. Quack B, Speed RM, Luciani JM, Noel B, Guichaoua M, Chandley AC. Cytogenet Cell Genet; 1988; 48(1):43-7. PubMed ID: 3180846 [Abstract] [Full Text] [Related]
2. A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I of meiosis. Chandley AC, Speed RM, McBeath S, Hargreave TB. Cytogenet Cell Genet; 1986; 41(3):145-53. PubMed ID: 3956264 [Abstract] [Full Text] [Related]
10. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report. Pinho MJ, Neves R, Costa P, Ferrás C, Sousa M, Alves C, Almeida C, Fernandes S, Silva J, Ferrás L, Barros A. Hum Reprod; 2005 Mar 20; 20(3):689-96. PubMed ID: 15665019 [Abstract] [Full Text] [Related]
11. [Pachytene stage of meiosis in an infertile man carrying a reciprocal translocation between two acrocentric chromosomes]. North MO, Guichaoua MR, Delafontaine D, Luciani JM. Ann Genet; 1994 Mar 20; 37(1):26-9. PubMed ID: 8010709 [Abstract] [Full Text] [Related]
13. Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21). Gabriel-Robez O, Ratomponirina C, Dutrillaux B, Carré-Pigeon F, Rumpler Y. Cytogenet Cell Genet; 1986 Mar 20; 43(3-4):154-60. PubMed ID: 3802918 [Abstract] [Full Text] [Related]
16. Meiotic defects and decreased expression of genes located around the chromosomal breakpoint in the testis of a patient with a novel 46,X,t(Y;1)(p11.3;p31) translocation. Li G, Iqbal F, Wang L, Xu Z, Che X, Yu W, Shi L, Guo T, Zhou G, Jiang X, Zhang H, Zhang Y, Yu D. Int J Mol Med; 2017 Aug 20; 40(2):367-377. PubMed ID: 28627638 [Abstract] [Full Text] [Related]