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Page 1
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Kashiyama K, Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T. Kashiyama K, et al. Among authors: lewin so. Am J Hum Genet. 2013 May 2;92(5):807-19. doi: 10.1016/j.ajhg.2013.04.007. Epub 2013 Apr 25. Am J Hum Genet. 2013. PMID: 23623389 Free PMC article.
Polytopic anomalies with agenesis of the lower vertebral column.
Bohring A, Lewin SO, Reynolds JF, Voigtländer T, Rittinger O, Carey JC, Köpernik M, Smith R, Zackai EH, Leonard NJ, Gritter HL, Bamforth JS, Okun N, McLeod DR, Super M, Powell P, Mundlos S, Hennekam RC, van Langen IM, Viskochil DH, Wiedemann HR, Opitz JM. Bohring A, et al. Among authors: lewin so. Am J Med Genet. 1999 Nov 19;87(2):99-114. Am J Med Genet. 1999. PMID: 10533024 Review.
German syndrome in sibs.
Lewin SO, Hughes HE. Lewin SO, et al. Am J Med Genet. 1987 Feb;26(2):385-90. doi: 10.1002/ajmg.1320260217. Am J Med Genet. 1987. PMID: 3812590
The value of examining spontaneously aborted human embryos and placentas.
Bruyere HJ Jr, Arya S, Kozel JS, Gilbert EF, FitzGerald JM, Reynolds JF Jr, Lewin SO, Opitz JM. Bruyere HJ Jr, et al. Among authors: lewin so. Birth Defects Orig Artic Ser. 1987;23(1):169-78. Birth Defects Orig Artic Ser. 1987. PMID: 3580546 No abstract available.
12 results