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The role of cytologic NOR variants in the etiology of trisomy 21.
Spinner NB, Eunpu DL, Schmickel RD, Zackai EH, McEldrew D, Bunin GR, McDermid H, Emanuel BS. Spinner NB, et al. Among authors: eunpu dl. Am J Hum Genet. 1989 May;44(5):631-8. Am J Hum Genet. 1989. PMID: 2523191 Free PMC article. Review.
Holoprosencephaly in a newborn girl with 46,XX,i(18q).
Spinner NB, Eunpu DL, Austria JR, Mamunes P. Spinner NB, et al. Among authors: eunpu dl. Am J Med Genet. 1991 Apr 1;39(1):11-2. doi: 10.1002/ajmg.1320390104. Am J Med Genet. 1991. PMID: 1867253
Direct DNA testing for fragile X syndrome.
Ramos FJ, Eunpu DL, Finucane B, Pfendner EG. Ramos FJ, et al. Among authors: eunpu dl. Am J Dis Child. 1993 Nov;147(11):1231-5. doi: 10.1001/archpedi.1993.02160350105016. Am J Dis Child. 1993. PMID: 7901988
Trisomy 21: rate in second-degree relatives.
Eunpu DL, McDonald DM, Zackai EH. Eunpu DL, et al. Am J Med Genet. 1986 Oct;25(2):361-3. doi: 10.1002/ajmg.1320250222. Am J Med Genet. 1986. PMID: 2946225
23 results