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A genetic linkage map of 27 markers on human chromosome 21.
Petersen MB, Slaugenhaupt SA, Lewis JG, Warren AC, Chakravarti A, Antonarakis SE. Petersen MB, et al. Among authors: lewis jg. Genomics. 1991 Mar;9(3):407-19. doi: 10.1016/0888-7543(91)90406-5. Genomics. 1991. PMID: 1674496 Free article.
A genetic linkage map of 17 markers on human chromosome 21.
Warren AC, Slaugenhaupt SA, Lewis JG, Chakravarti A, Antonarakis SE. Warren AC, et al. Among authors: lewis jg. Genomics. 1989 May;4(4):579-91. doi: 10.1016/0888-7543(89)90282-6. Genomics. 1989. PMID: 2568330
Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Collins FA, et al. Among authors: lewis jg. Am J Med Genet. 1992 Jan 1;42(1):127-34. doi: 10.1002/ajmg.1320420126. Am J Med Genet. 1992. PMID: 1308352
DNA polymorphism analysis in families with recurrence of free trisomy 21.
Pangalos CG, Talbot CC Jr, Lewis JG, Adelsberger PA, Petersen MB, Serre JL, Rethoré MO, de Blois MC, Parent P, Schinzel AA, et al. Pangalos CG, et al. Among authors: lewis jg. Am J Hum Genet. 1992 Nov;51(5):1015-27. Am J Hum Genet. 1992. PMID: 1415248 Free PMC article.
PAM-free diagnostics with diverse type V CRISPR-Cas systems.
Rananaware SR, Meister KS, Shoemaker GM, Vesco EK, Sandoval LSW, Lewis JG, Bodin AP, Karalkar VN, Lange IH, Pizzano BLM, Chang M, Ahmadimashhadi MR, Flannery SJ, Nguyen LT, Wang GP, Jain PK. Rananaware SR, et al. Among authors: lewis jg. medRxiv [Preprint]. 2024 May 3:2024.05.02.24306194. doi: 10.1101/2024.05.02.24306194. medRxiv. 2024. PMID: 38746294 Free PMC article. Preprint.
233 results