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Cytological studies of meiotic recombination in human males.
Hassold T, Judis L, Chan ER, Schwartz S, Seftel A, Lynn A. Hassold T, et al. Among authors: schwartz s. Cytogenet Genome Res. 2004;107(3-4):249-55. doi: 10.1159/000080602. Cytogenet Genome Res. 2004. PMID: 15467369
Synaptic defects at meiosis I and non-obstructive azoospermia.
Topping D, Brown P, Judis L, Schwartz S, Seftel A, Thomas A, Hassold T. Topping D, et al. Among authors: schwartz s. Hum Reprod. 2006 Dec;21(12):3171-7. doi: 10.1093/humrep/del281. Epub 2006 Jul 22. Hum Reprod. 2006. PMID: 16861745
Maternal folate polymorphisms and the etiology of human nondisjunction.
Hassold TJ, Burrage LC, Chan ER, Judis LM, Schwartz S, James SJ, Jacobs PA, Thomas NS. Hassold TJ, et al. Among authors: schwartz s. Am J Hum Genet. 2001 Aug;69(2):434-9. doi: 10.1086/321971. Epub 2001 Jul 5. Am J Hum Genet. 2001. PMID: 11443546 Free PMC article.
Punctuated duplication seeding events during the evolution of human chromosome 2p11.
Horvath JE, Gulden CL, Vallente RU, Eichler MY, Ventura M, McPherson JD, Graves TA, Wilson RK, Schwartz S, Rocchi M, Eichler EE. Horvath JE, et al. Among authors: schwartz s. Genome Res. 2005 Jul;15(7):914-27. doi: 10.1101/gr.3916405. Epub 2005 Jun 17. Genome Res. 2005. PMID: 15965031 Free PMC article.
5,615 results