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Authors: Erickson, RP Dagenais, SL Caulder, MS Downs, CA Herman, G Jones, MC Kerstjens-Frederikse, WS Lidral, AC McDonald, M Nelson, CC Witte, M Glover, TW
Citation: Rp. Erickson et al., Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations, J MED GENET, 38(11), 2001, pp. 761-766

Authors: Kerstjens-Frederikse, WS Kurahashi, H Driscoll, DA Budarf, ML Emanuel, BS Beatty, B Scheidl, T Siegel-Bartelt, J Henderson, K Cytrynbaum, C Nie, G Teshima, I
Citation: Ws. Kerstjens-frederikse et al., Microdeletion 22q11.2: clinical data and deletion size, J MED GENET, 36(9), 1999, pp. 721-723

Authors: Kerstjens-Frederikse, WS Hofstra, RMW van Essen, AJ Meijers, JHC Buys, CHCM
Citation: Ws. Kerstjens-frederikse et al., A Hirschsprung disease locus at 22q11?, J MED GENET, 36(3), 1999, pp. 221-224
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