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Literature DB >> 8908177

Human aneuploidy: incidence, origin, and etiology.

T Hassold¹, M Abruzzo, K Adkins, D Griffin, M Merrill, E Millie, D Saker, J Shen, M Zaragoza.

Abstract

Entities: Disease Species

Mesh：

Year: 1996 PMID： 8908177 DOI： 10.1002/(SICI)1098-2280(1996)28:3<167::AID-EM2>3.0.CO;2-B

Source DB: PubMed Journal: Environ Mol Mutagen ISSN： 0893-6692 Impact factor: 3.216

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Cited

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107 in total

1. Heritability of the maternal meiotic drive system linked to Om and high-resolution mapping of the Responder locus in mouse.

Authors: F Pardo-Manuel De Villena; E de La Casa-Esperón; J W Williams; J M Malette; M Rosa; C Sapienza
Journal: Genetics Date: 2000-05 Impact factor: 4.562

2. Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21.

Authors: T Wiltshire; M Pletcher; S E Cole; M Villanueva; B Birren; J Lehoczky; K Dewar; R H Reeves
Journal: Genome Res Date: 1999-12 Impact factor: 9.043

3. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Authors: Tiffany Renee Oliver; Stuart W Tinker; Emily Graves Allen; Natasha Hollis; Adam E Locke; Lora J H Bean; Reshmi Chowdhury; Ferdouse Begum; Mary Marazita; Vivian Cheung; Eleanor Feingold; Stephanie L Sherman
Journal: Hum Genet Date: 2011-12-09 Impact factor: 4.132

Review 4. The cytogenetics of preimplantation human development: insights provided by traditional and novel techniques.

Authors: Helen G Tempest; Darren K Griffin
Journal: Chromosoma Date: 2005-10-15 Impact factor: 4.316

5. The National Down Syndrome Project: design and implementation.

Authors: Sallie B Freeman; Emily G Allen; Cindy L Oxford-Wright; Stuart W Tinker; Charlotte Druschel; Charlotte A Hobbs; Leslie A O'Leary; Paul A Romitti; Marjorie H Royle; Claudine P Torfs; Stephanie L Sherman
Journal: Public Health Rep Date: 2007 Jan-Feb Impact factor: 2.792

Human aneuploidy: incidence, origin, and etiology.

1. Heritability of the maternal meiotic drive system linked to Om and high-resolution mapping of the Responder locus in mouse.

2. Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21.

3. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Review 4. The cytogenetics of preimplantation human development: insights provided by traditional and novel techniques.

5. The National Down Syndrome Project: design and implementation.

6. Chromosomal mosaicism in mouse two-cell embryos after paternal exposure to acrylamide.

7. TroX: a new method to learn about the genesis of aneuploidy from trisomic products of conception.

8. Spindle checkpoint deficiency is tolerated by murine epidermal cells but not hair follicle stem cells.

Review 9. Developmental Programming of Ovarian Functions and Dysfunctions.

10. Investigation of factors associated with paternal nondisjunction of chromosome 21.