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Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study.
Mekori-Domachevsky E, Guri Y, Yi J, Weisman O, Calkins ME, Tang SX, Gross R, McDonald-McGinn DM, Emanuel BS, Zackai EH, Zalsman G, Weizman A, Gur RC, Gur RE, Gothelf D. Mekori-Domachevsky E, et al. Among authors: emanuel bs. Schizophr Res. 2017 Oct;188:42-49. doi: 10.1016/j.schres.2016.12.023. Epub 2016 Dec 29. Schizophr Res. 2017. PMID: 28041919 Free PMC article.
Interstitial deletion of 4(q21q25) in a liveborn male.
Rose NC, Schneider A, McDonald-McGinn DM, Caserta C, Emanuel BS, Zackai EH. Rose NC, et al. Among authors: emanuel bs. Am J Med Genet. 1991 Jul 1;40(1):77-9. doi: 10.1002/ajmg.1320400115. Am J Med Genet. 1991. PMID: 1887853 Review.
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: emanuel bs. Am J Hum Genet. 1989 May;44(5):631-8. Am J Hum Genet. 1989. PMID: 2523191 Free PMC article. Review.
Congenital glaucoma associated with a chromosomal abnormality.
Stambolian D, Quinn G, Emanuel BS, Zackai E. Stambolian D, et al. Among authors: emanuel bs. Am J Ophthalmol. 1988 Nov 15;106(5):625-7. doi: 10.1016/0002-9394(88)90599-5. Am J Ophthalmol. 1988. PMID: 3189479 No abstract available.
399 results