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Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.
Antonarakis SE, Rossiter JP, Young M, Horst J, de Moerloose P, Sommer SS, Ketterling RP, Kazazian HH Jr, Négrier C, Vinciguerra C, Gitschier J, Goossens M, Girodon E, Ghanem N, Plassa F, Lavergne JM, Vidaud M, Costa JM, Laurian Y, Lin SW, Lin SR, Shen MC, Lillicrap D, Taylor SA, Windsor S, Valleix SV, Nafa K, Sultan Y, Delpech M, Vnencak-Jones CL, Phillips JA 3rd, Ljung RC, Koumbarelis E, Gialeraki A, Mandalaki T, Jenkins PV, Collins PW, Pasi KJ, Goodeve A, Peake I, Preston FE, Schwartz M, Scheibel E, Ingerslev J, Cooper DN, Millar DS, Kakkar VV, Giannelli F, Naylor JA, Tizzano EF, Baiget M, Domenech M, Altisent C, Tusell J, Beneyto M, Lorenzo JI, Gaucher C, Mazurier C, Peerlinck K, Matthijs G, Cassiman JJ, Vermylen J, Mori PG, Acquila M, Caprino D, Inaba H. Antonarakis SE, et al. Among authors: cooper dn. Blood. 1995 Sep 15;86(6):2206-12. Blood. 1995. PMID: 7662970 Free article.
Recurrent deletion in the human antithrombin III gene.
Grundy CB, Thomas F, Millar DS, Krawczak M, Melissari E, Lindo V, Moffat E, Kakkar VV, Cooper DN. Grundy CB, et al. Among authors: cooper dn. Blood. 1991 Aug 15;78(4):1027-32. Blood. 1991. PMID: 1868237 Free article.
Disease-causing mutations in the human genome.
Antonarakis SE, Krawczak M, Cooper DN. Antonarakis SE, et al. Among authors: cooper dn. Eur J Pediatr. 2000 Dec;159 Suppl 3:S173-8. doi: 10.1007/pl00014395. Eur J Pediatr. 2000. PMID: 11216894 Review.
599 results