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Interrupted aortic arch: an epidemiologic study.
Loffredo CA, Ferencz C, Wilson PD, Lurie IW. Loffredo CA, et al. Teratology. 2000 May;61(5):368-75. doi: 10.1002/(SICI)1096-9926(200005)61:5<368::AID-TERA8>3.0.CO;2-N. Teratology. 2000. PMID: 10777832
VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal community.
Lurie IW, Ferencz C. Lurie IW, et al. Am J Med Genet. 1997 May 16;70(2):144-9. doi: 10.1002/(sici)1096-8628(19970516)70:2<144::aid-ajmg8>;2-y. Am J Med Genet. 1997. PMID: 9128933 Review.
The acrocallosal syndrome: expansion of the phenotypic spectrum.
Lurie IW, Naumchik IV, Wulfsberg EA. Lurie IW, et al. Clin Dysmorphol. 1994 Jan;3(1):31-4. Clin Dysmorphol. 1994. PMID: 8205323
Trisomy 4p and ocular defects.
Lurie IW, Samochvalov VA. Lurie IW, et al. Br J Ophthalmol. 1994 May;78(5):415-7. doi: 10.1136/bjo.78.5.415. Br J Ophthalmol. 1994. PMID: 8025082 Free PMC article. No abstract available.
Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
Lurie IW, Schwartz MF, Schwartz S, Cohen MM. Lurie IW, et al. Am J Med Genet. 1995 Jan 2;55(1):62-6. doi: 10.1002/ajmg.1320550117. Am J Med Genet. 1995. PMID: 7702099 Review.
Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance.
Lurie IW, Wulfsberg EA, Prabhakar G, Rosenblum-Vos LS, Supovitz KR, Cohen MM. Lurie IW, et al. Clin Genet. 1994 Sep;46(3):244-7. doi: 10.1111/j.1399-0004.1994.tb04234.x. Clin Genet. 1994. PMID: 7529663 Review.
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