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Trisomy in humans: incidence, origin and etiology.
Hassold T, Hunt PA, Sherman S. Hassold T, et al. Curr Opin Genet Dev. 1993 Jun;3(3):398-403. doi: 10.1016/0959-437x(93)90111-2. Curr Opin Genet Dev. 1993. PMID: 8353412 Review.
Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew.
Hassold T, Hunt P. Hassold T, et al. Curr Opin Pediatr. 2009 Dec;21(6):703-8. doi: 10.1097/MOP.0b013e328332c6ab. Curr Opin Pediatr. 2009. PMID: 19881348 Free PMC article. Review.
The origin of human aneuploidy: where we have been, where we are going.
Hassold T, Hall H, Hunt P. Hassold T, et al. Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R203-8. doi: 10.1093/hmg/ddm243. Hum Mol Genet. 2007. PMID: 17911163 Review.
The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.
Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. Hall HE, et al. Among authors: hassold t. Am J Med Genet A. 2007 Oct 1;143A(19):2249-55. doi: 10.1002/ajmg.a.31918. Am J Med Genet A. 2007. PMID: 17705154
An algorithm for determining the origin of trisomy and the positions of chiasmata from SNP genotype data.
Gabriel AS, Hassold TJ, Thornhill AR, Affara NA, Handyside AH, Griffin DK. Gabriel AS, et al. Among authors: hassold tj. Chromosome Res. 2011 Feb;19(2):155-63. doi: 10.1007/s10577-010-9181-4. Epub 2011 Jan 12. Chromosome Res. 2011. PMID: 21225334
The origin of trisomy 13.
Hall HE, Chan ER, Collins A, Judis L, Shirley S, Surti U, Hoffner L, Cockwell AE, Jacobs PA, Hassold TJ. Hall HE, et al. Among authors: hassold tj. Am J Med Genet A. 2007 Oct 1;143A(19):2242-8. doi: 10.1002/ajmg.a.31913. Am J Med Genet A. 2007. PMID: 17853475
Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male.
Brown PW, Judis L, Chan ER, Schwartz S, Seftel A, Thomas A, Hassold TJ. Brown PW, et al. Among authors: hassold tj. Am J Hum Genet. 2005 Oct;77(4):556-66. doi: 10.1086/468188. Epub 2005 Aug 16. Am J Hum Genet. 2005. PMID: 16175502 Free PMC article.
SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction.
Hodges CA, Revenkova E, Jessberger R, Hassold TJ, Hunt PA. Hodges CA, et al. Among authors: hassold tj. Nat Genet. 2005 Dec;37(12):1351-5. doi: 10.1038/ng1672. Epub 2005 Oct 30. Nat Genet. 2005. PMID: 16258540
Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome.
Mann MB, Hodges CA, Barnes E, Vogel H, Hassold TJ, Luo G. Mann MB, et al. Among authors: hassold tj. Hum Mol Genet. 2005 Mar 15;14(6):813-25. doi: 10.1093/hmg/ddi075. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703196
Meiotic exchange and segregation in female mice heterozygous for paracentric inversions.
Koehler KE, Millie EA, Cherry JP, Schrump SE, Hassold TJ. Koehler KE, et al. Among authors: hassold tj. Genetics. 2004 Mar;166(3):1199-214. doi: 10.1534/genetics.166.3.1199. Genetics. 2004. PMID: 15082541 Free PMC article.
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