Embryonic and not maternal trisomy causes developmental attenuation in the Ts65Dn mouse model for Down syndrome

Author:

Blazek Joshua D.,Billingsley Cherie N.,Newbauer Abby,Roper Randall J.

Publisher

Wiley

Subject

Developmental Biology

Reference47 articles.

1. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21;Arron;Nature,2006

2. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse;Baxter;Hum Mol Genet,2000

3. Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase;Bowes;Proc Natl Acad Sci U S A,1993

4. Ultrasound diagnosis of mouse pregnancy and gestational staging;Brown;Comp Med,2006

5. Improved national prevalence estimates for 18 selected major birth defects--United States, 1999-2001;Centers for Disease Control and Prevention;MMWR Morb Mortal Wkly Rep,2006

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