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Further delineation of the branchio-oculo-facial syndrome.
Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Among authors: lurie iw. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Free article. Review.
Trisomy 2p: analysis of unusual phenotypic findings.
Lurie IW, Ilyina HG, Gurevich DB, Rumyantseva NV, Naumchik IV, Castellan C, Hoeller A, Schinzel A. Lurie IW, et al. Am J Med Genet. 1995 Jan 16;55(2):229-36. doi: 10.1002/ajmg.1320550216. Am J Med Genet. 1995. PMID: 7717424 Review.
Trisomy 20p: case report and genetic review.
Lurie IW, Rumyantseva NV, Zaletajev DV, Gurevich DB, Korotkova IA. Lurie IW, et al. J Genet Hum. 1985 Jan;33(1):67-75. J Genet Hum. 1985. PMID: 3981145
Genetics of the Costello syndrome.
Lurie IW. Lurie IW. Am J Med Genet. 1994 Sep 1;52(3):358-9. doi: 10.1002/ajmg.1320520321. Am J Med Genet. 1994. PMID: 7528974 Review.
Atypical case of Aarskog syndrome.
Mikelsaar RV, Lurie IW. Mikelsaar RV, et al. Among authors: lurie iw. J Med Genet. 1992 May;29(5):349-50. doi: 10.1136/jmg.29.5.349. J Med Genet. 1992. PMID: 1583665 Free PMC article. No abstract available.
99 results