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An analysis of a large postlingually deaf family with hereditary non-syndromic profound hearing loss
Authors:
Angeli, SI
Naranjo, C
Friedman, RA
Naranjo, A
Henriquez, O
Fischel-Ghodsian, N
Chiossone, E
Citation: Si. Angeli et al., An analysis of a large postlingually deaf family with hereditary non-syndromic profound hearing loss, ACT OTO-LAR, 119(2), 1999, pp. 158-162
Authors:
Shohat, M
Lotan, R
Magal, N
Danon, Y
Ogur, G
Tokguz, G
Schlezinger, M
Schwabe, A
Halpern, G
Fischel-Ghodsian, N
Kastner, D
Shohat, T
Rotter, JI
Citation: M. Shohat et al., Amyloidosis in familial Mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus, MOL GEN MET, 65(3), 1998, pp. 197-202
Authors:
Centola, M
Chen, XG
Sood, R
Deng, ZM
Aksentijevich, I
Blake, T
Ricke, DO
Chen, X
Wood, G
Zaks, N
Richards, N
Krizman, D
Mansfield, E
Apostolou, S
Liu, JM
Shafran, N
Vedula, A
Hamon, M
Cercek, A
Kahan, T
Gumucio, D
Callen, DF
Richards, RI
Moyzis, RK
Doggett, NA
Collins, FS
Liu, PP
Fischel-Ghodsian, N
Kastner, DL
Citation: M. Centola et al., Construction of an similar to 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3, GENOME RES, 8(11), 1998, pp. 1172-1191
Authors:
Hsu, WT
Shchepin, DA
Mao, R
Berry-Kravis, E
Garber, AP
Fischel-Ghodsian, N
Falk, RE
Carlson, DE
Roeder, ER
Leeth, EA
Hajianpour, MJ
Wang, JCC
Rosenblum-Vos, LS
Bhatt, SD
Karson, EM
Hux, CH
Trunca, C
Bialer, MG
Linn, SK
Schreck, RR
Citation: Wt. Hsu et al., Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases, AM J MED G, 80(5), 1998, pp. 473-480