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Year Number of Results
1974 3
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1986 3
1987 4
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1993 7
1995 1
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2024 1

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31 results

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Page 1
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Najjar syndrome revisited.
Thomas IT, Jewett T, Lantz P, Covitz W, Garber P, Berry MN. Thomas IT, et al. Am J Med Genet. 1993 Dec 1;47(8):1151-2. doi: 10.1002/ajmg.1320470803. Am J Med Genet. 1993. PMID: 8291546
Williams syndrome: autosomal dominant inheritance.
Morris CA, Thomas IT, Greenberg F. Morris CA, et al. Among authors: thomas it. Am J Med Genet. 1993 Sep 15;47(4):478-81. doi: 10.1002/ajmg.1320470409. Am J Med Genet. 1993. PMID: 8256809
Isolated and syndromic cryptophthalmos.
Thomas IT, Frias JL, Felix V, Sanchez de Leon L, Hernandez RA, Jones MC. Thomas IT, et al. Am J Med Genet. 1986 Sep;25(1):85-98. doi: 10.1002/ajmg.1320250111. Am J Med Genet. 1986. PMID: 3099574 Review.
31 results