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Results: 1-8 |
Results: 8
Autosomal recessive lissencephaly with cerebellar hypoplasia is associatedwith human RELN mutations (vol 26, pg 93, 2000)
Authors: Hong, SE
Citation: Se. Hong, Autosomal recessive lissencephaly with cerebellar hypoplasia is associatedwith human RELN mutations (vol 26, pg 93, 2000), NAT GENET, 27(2), 2001, pp. 225-225
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females
Authors: Sheen, VL Dixon, PH Fox, JW Hong, SE Kinton, L Sisodiya, SM Duncan, JS Dubeau, F Scheffer, IE Schachter, SC Wilner, A Henchy, R Crino, P Kamuro, K DiMario, F Berg, M Kuzniecky, R Cole, AJ Bromfield, E Biber, M Schomer, D Wheless, J Silver, K Mochida, GH Berkovic, SF Andermann, F Andermann, E Dobyns, WB Wood, NW Walsh, CA
Citation: Vl. Sheen et al., Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females, HUM MOL GEN, 10(17), 2001, pp. 1775-1783
Novel organic bottom antireflective coating materials for 193 nm lithography
Authors: Jung, MH Hong, SE Jung, JC Lee, G Baik, KH
Citation: Mh. Jung et al., Novel organic bottom antireflective coating materials for 193 nm lithography, JPN J A P 1, 39(12B), 2000, pp. 6961-6965
Autosomal recessive lissencephaly with cerebellar hypoplasia is associatedwith human RELN mutations
Authors: Hong, SE Shugart, YY Huang, DT Shahwan, SA Grant, PE Hourihane, JOB Martin, NDT Walsh, CA
Citation: Se. Hong et al., Autosomal recessive lissencephaly with cerebellar hypoplasia is associatedwith human RELN mutations, NAT GENET, 26(1), 2000, pp. 93-96
Hemophilic pseudotumor of the ulna treated with low dose radiation therapy: A case report
Authors: Kang, JO Cho, YJ Yoo, MC Hong, SE
Citation: Jo. Kang et al., Hemophilic pseudotumor of the ulna treated with low dose radiation therapy: A case report, J KOR MED S, 15(5), 2000, pp. 601-603
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome
Authors: Gleeson, JG Minnerath, SR Fox, JW Allen, KM Luo, RF Hong, SE Berg, MJ Kuzniecky, R Reitnauer, PJ Borgatti, R Mira, AP Guerrini, R Holmes, GL Rooney, CM Berkovic, S Scheffer, I Cooper, EC Ricci, S Cusmai, R Crawford, TO Leroy, R Andermann, E Wheless, JW Dobyns, WB Ross, ME Walsh, CA
Citation: Jg. Gleeson et al., Characterization of mutations in the gene doublecortin in patients with double cortex syndrome, ANN NEUROL, 45(2), 1999, pp. 146-153
Long-term comparison of a newly designed gold implant with the conventional implant in facial nerve paralysis
Authors: Choi, HY Hong, SE Lew, JM
Citation: Hy. Choi et al., Long-term comparison of a newly designed gold implant with the conventional implant in facial nerve paralysis, PLAS R SURG, 104(6), 1999, pp. 1624-1634
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
Authors: Fox, JW Lamperti, ED Eksioglu, YZ Hong, SE Feng, YY Graham, DA Scheffer, IE Dobyns, WB Hirsch, BA Radtke, RA Berkovic, SF Huttenlocher, PR Walsh, CA
Citation: Jw. Fox et al., Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia, NEURON, 21(6), 1998, pp. 1315-1325
Risultati: 1-8 |