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Maternal effect for DNA mismatch repair in the mouse.
Gurtu VE, Verma S, Grossmann AH, Liskay RM, Skarnes WC, Baker SM. Gurtu VE, et al. Among authors: grossmann ah. Genetics. 2002 Jan;160(1):271-7. doi: 10.1093/genetics/160.1.271. Genetics. 2002. PMID: 11805062 Free PMC article.
NF1 Somatic Mutation in Dystrophic Scoliosis.
Margraf RL, VanSant-Webb C, Mao R, Viskochil DH, Carey J, Hanson H, D'Astous J, Grossmann A, Stevenson DA. Margraf RL, et al. J Mol Neurosci. 2019 May;68(1):11-18. doi: 10.1007/s12031-019-01277-0. Epub 2019 Feb 18. J Mol Neurosci. 2019. PMID: 30778836
Molecular testing in malignant melanoma.
Grossmann AH, Grossmann KF, Wallander ML. Grossmann AH, et al. Among authors: grossmann kf. Diagn Cytopathol. 2012 Jun;40(6):503-10. doi: 10.1002/dc.22810. Diagn Cytopathol. 2012. PMID: 22619125 Review.
Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice.
Chan AC, Drakos SG, Ruiz OE, Smith AC, Gibson CC, Ling J, Passi SF, Stratman AN, Sacharidou A, Revelo MP, Grossmann AH, Diakos NA, Davis GE, Metzstein MM, Whitehead KJ, Li DY. Chan AC, et al. Among authors: grossmann ah. J Clin Invest. 2011 May;121(5):1871-81. doi: 10.1172/JCI44393. Epub 2011 Apr 1. J Clin Invest. 2011. PMID: 21490399 Free PMC article.
Fine-needle aspiration diagnosis of an intraosseous amyloidoma.
Factor RE, Layfield LJ, Grossmann AH, Crim JR, Price SL, Randall RL. Factor RE, et al. Among authors: grossmann ah. Diagn Cytopathol. 2012 Aug;40 Suppl 2:E114-7. doi: 10.1002/dc.21686. Epub 2011 May 4. Diagn Cytopathol. 2012. PMID: 21548115
43 results