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Blair E

References (2)

Title : Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826
Author(s) : Harrison V , Connell L , Hayesmoore J , McParland J , Pike MG , Blair E
Ref : American Journal of Medicine Genet A , 155A :2826 , 2011
Abstract :
PubMedSearch : Harrison_2011_Am.J.Med.Genet.A_155A_2826
PubMedID: 21964664

Title : Complete genome sequence of Neisseria meningitidis serogroup B strain MC58 - Tettelin_2000_Science_287_1809
Author(s) : Tettelin H , Saunders NJ , Heidelberg J , Jeffries AC , Nelson KE , Eisen JA , Ketchum KA , Hood DW , Peden JF , Dodson RJ , Nelson WC , Gwinn ML , Deboy R , Peterson JD , Hickey EK , Haft DH , Salzberg SL , White O , Fleischmann RD , Dougherty BA , Mason T , Ciecko A , Parksey DS , Blair E , Cittone H , Clark EB , Cotton MD , Utterback TR , Khouri H , Qin H , Vamathevan J , Gill J , Scarlato V , Masignani V , Pizza M , Grandi G , Sun L , Smith HO , Fraser CM , Moxon ER , Rappuoli R , Venter JC
Ref : Science , 287 :1809 , 2000
Abstract :
PubMedSearch : Tettelin_2000_Science_287_1809
PubMedID: 10710307
Gene_locus related to this paper: neigo-pip , neima-metx , neimb-q9k0t9 , neime-ESD , neime-NMA2216 , neime-NMB0276 , neime-NMB0868 , neime-NMB1828 , neime-NMB1877