Authors: MALZAC P BIANCALANA V VOELCKEL MA MONCLA A PELLISSIER MC BOCCACCIO I MATTEI JF

Citation: P. Malzac et al., UNEXPECTED INHERITANCE OF THE (CGG)(N) TRINUCLEOTIDE EXPANSION IN A FRAGILE-X SYNDROME FAMILY, European journal of human genetics, 4(1), 1996, pp. 8-12

Authors: ALESSI MC AILLAUD MF PAUT O ROQUELAURE B ALHENCGELAS M PELLISSIER MC GHANEN N JUHANVAGUE I

Citation: Mc. Alessi et al., PURPURA FULMINANS IN A PATIENT HOMOZYGOUS FOR A MUTATION IN THE PROTEIN-C GENE - PRENATAL-DIAGNOSIS IN A SUBSEQUENT PREGNANCY, Thrombosis and haemostasis, 75(3), 1996, pp. 525-526

Authors: MALZAC P BIANCALANA V VOELCKEL MA MONCLA A PELLISSIER MC BOCCACCIO I MANDEL JL MATTEI JF

Citation: P. Malzac et al., A RARE EXAMPLE OF A REVERSE MUTATION IN A FRAGILE-X SYNDROME FAMILY, American journal of medical genetics, 64(1), 1996, pp. 17-17

Authors: PHILIP N PIQUET C LEVY A SCHEINER C PELLISSIER MC GAMERRE M

Citation: N. Philip et al., FETOPLACENTAL DISCREPANCY FOR TRISOMY-22 AND GOLDENHAR SEQUENCE, American journal of human genetics, 53(3), 1993, pp. 485-485