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Family Health Leaders: Lessons on Living with Li-Fraumeni Syndrome across Generations.
Pantaleao A, Young JL, Epstein NB, Carlson M, Bremer RC, Khincha PP, Peters JA, Greene MH, Roy K, Achatz MI, Savage SA, Werner-Lin A. Pantaleao A, et al. Among authors: khincha pp. Fam Process. 2020 Dec;59(4):1648-1663. doi: 10.1111/famp.12497. Epub 2019 Oct 24. Fam Process. 2020. PMID: 31647118 Free PMC article.
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.
Khincha PP, Bertuch AA, Agarwal S, Townsley DM, Young NS, Keel S, Shimamura A, Boulad F, Simoneau T, Justino H, Kuo C, Artandi S, McCaslin C, Cox DW, Chaffee S, Collins BF, Giri N, Alter BP, Raghu G, Savage SA. Khincha PP, et al. Eur Respir J. 2017 Jan 25;49(1):1601640. doi: 10.1183/13993003.01640-2016. Print 2017 Jan. Eur Respir J. 2017. PMID: 27824607 Free PMC article.
Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.
Mirabello L, Khincha PP, Ellis SR, Giri N, Brodie S, Chandrasekharappa SC, Donovan FX, Zhou W, Hicks BD, Boland JF, Yeager M, Jones K, Zhu B, Wang M, Alter BP, Savage SA. Mirabello L, et al. Among authors: khincha pp. J Med Genet. 2017 Jun;54(6):417-425. doi: 10.1136/jmedgenet-2016-104346. Epub 2017 Mar 9. J Med Genet. 2017. PMID: 28280134 Clinical Trial.
48 results