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Results: 5

Authors: RUND D SCHAAP T GILLIS S
Citation: D. Rund et al., INTENSIVE PLASMAPHERESIS FOR SEVERE THROMBOTIC THROMBOCYTOPENIC PURPURA - LONG-TERM CLINICAL OUTCOME, Journal of clinical apheresis, 12(4), 1997, pp. 194-195

Authors: DAR H SCHAAP T BAITOR H BOROCHOWITZ Z GELMANKOHAN Z CHEMKE T CHAKI R COHEN H FALIKBORENSTEIN Z CHEMKE J
Citation: H. Dar et al., ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OFFOUNDER CHROMOSOMES(), Israel journal of medical sciences, 31(5), 1995, pp. 323-325

Authors: SCHAAP T
Citation: T. Schaap, CONFIDENTIALITY IN COUNSELING FOR X-LINKED CONDITIONS, Clinical genetics, 47(3), 1995, pp. 155-157

Authors: ROUSSEAU F HEITZ D TARLETON J MACPHERSON J MALMGREN H DAHL N BARNICOAT A MATHEW C MORNET E TEJADA I MADDALENA A SPIEGEL R SCHINZEL A MARCOS JAG SCHORDERET DF SCHAAP T MACCIONI L RUSSO S JACOBS PA SCHWARTZ C MANDEL JL
Citation: F. Rousseau et al., A MULTICENTER STUDY ON GENOTYPE-PHENOTYPE CORRELATIONS IN THE FRAGILE-X-SYNDROME, USING DIRECT DIAGNOSIS WITH PROBE STB-12.3 - THE FIRST 2,253 CASES, American journal of human genetics, 55(2), 1994, pp. 225-237

Authors: ROUSSEAU F HEITZ D TARLETON J MACPHERSON J PETTERSON U MATHEW C MORNET E MADDALENA A SCHINZEL A MARCOS JAG SCHORDERET DF SCHAAP T MACCIONI L RUSSO S JACOBS PA SCHWARTZ C MANDEL JL
Citation: F. Rousseau et al., A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES, American journal of human genetics, 53(3), 1993, pp. 78-78
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