Authors: BERNARD LE HUNTSMAN D RAHEMTULLAH A MCGILLIVRAY BC LANGLOIS S

Citation: Le. Bernard et al., 13 NOVEL FIBRILLIN-1 MUTATIONS DETECTED USING HETERODUPLEX ANALYSIS IN A SCREEN OF 44 INDIVIDUALS WITH CLASSICAL MARFAN-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1910-1910

Authors: DRUMHELLER T MCGILLIVRAY BC BEHRNER D MACLEOD P MCFADDEN DE ROBERSON J VENDITTI C CHORNEY K CHORNEY M SMITH DI

Citation: T. Drumheller et al., PRECISE LOCALIZATION OF 3P25 BREAKPOINTS IN 4 PATIENTS WITH THE 3P-SYNDROME, Journal of Medical Genetics, 33(10), 1996, pp. 842-847

Authors: CHOY FYM WEI C APPLEGARTH DA MCGILLIVRAY BC

Citation: Fym. Choy et al., DNA ANALYSIS OF AN UNCOMMON MISSENSE MUTATION IN A GAUCHER DISEASE PATIENT OF JEWISH-POLISH-RUSSIAN DESCENT, American journal of medical genetics, 51(2), 1994, pp. 156-160

Authors: VANALLEN MI MCGILLIVRAY BC LANGLOIS S

Citation: Mi. Vanallen et al., DIZYGOTIC TWINS DISCORDANT FOR STRUCTURAL ANOMALIES FROM VASCULAR DISRUPTION, Clinical research, 42(1), 1994, pp. 10000065-10000065

Authors: VANALLEN MI KALOUSEK DK CHERNOFF GF JURILOFF D HARRIS M MCGILLIVRAY BC YONG SL LANGLOIS S MACLEOD PM CHITAYAT D FRIEDMAN JM WILSON RD MCFADDEN D PANTZAR J RITCHIE S HALL JG

Citation: Mi. Vanallen et al., EVIDENCE FOR MULTISITE CLOSURE OF THE NEURAL-TUBE IN HUMANS, American journal of medical genetics, 47(5), 1993, pp. 723-743