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Results: 1-5 |
Results: 5

Authors: LANGLOIS S HUNTSMAN D RUPPS R KWONG LC MACLEOD P FREIDMAN JM
Citation: S. Langlois et al., NEUROFIBROMATOSIS TYPE-1 (NF1) IN COUSINS WITH UNAFFECTED PARENTS - NON-PENETRANCE OR COINCIDENTAL NEW MUTATIONS, American journal of human genetics, 61(4), 1997, pp. 584-584

Authors: DESILETS VA YONG SL KALOUSEK DK PANTZAR TJ KWONG LC SIEMENS C LANGLOIS S
Citation: Va. Desilets et al., MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-14, American journal of human genetics, 61(4), 1997, pp. 691-691

Authors: WILSON RD YONG SL YONG K WADSWORTH LD KWONG LC LANGLOIS S
Citation: Rd. Wilson et al., THALASSEMIA CARRIER SCREENING AND PRENATAL-DIAGNOSIS IN BRITISH-COLUMBIAS HIGH-RISK POPULATION, American journal of human genetics, 61(4), 1997, pp. 1327-1327

Authors: LANGLOIS S YONG SL WILSON RD KWONG LC KALOUSEK DK
Citation: S. Langlois et al., PRENATAL AND POSTNATAL-GROWTH FAILURE ASSOCIATED WITH MATERNAL HETERODISOMY FOR CHROMOSOME-7, Journal of Medical Genetics, 32(11), 1995, pp. 871-875

Authors: MCFADDEN DE KWONG LC YAM IYL LANGLOIS S
Citation: De. Mcfadden et al., PARENTAL ORIGIN OF TRIPLOIDY IN HUMAN FETUSES - EVIDENCE FOR GENOMIC IMPRINTING, Human genetics, 92(5), 1993, pp. 465-469
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