Authors: ALFORD RL DEMARCHI JM RICHARDS CS

Citation: Rl. Alford et al., FREQUENCY OF A DNA POLYMORPHISM AT POSITION Y231 IN THE ASPARTOACYLASE GENE AND ITS IMPACT ON DNA-BASED CARRIER TESTING FOR CANAVAN-DISEASEIN THE ASHKENAZI JEWISH POPULATION, Human mutation, 1998, pp. 161-162

Authors: DEMARCHI JM SUGARMAN EA ALLITTO BA

Citation: Jm. Demarchi et al., GONADAL MOSAICISM OF A RECOMBINANT CHROMOSOME IN A WOMAN SEEKING PRENATAL-DIAGNOSIS FOR SPINAL MUSCULAR-ATROPHY TYPE-I (WERDNIG-HOFFMAN-DISEASE), American journal of human genetics, 61(4), 1997, pp. 863-863

Authors: DEMARCHI JM CASKEY CT RICHARDS CS

Citation: Jm. Demarchi et al., POPULATION-SPECIFIC SCREENING BY MUTATION ANALYSIS FOR DISEASES FREQUENT IN ASHKENAZI JEWS, Human mutation, 8(2), 1996, pp. 116-125

Authors: DEMARCHI JM RICHARDS CS FENWICK RG PACE R BEAUDET AL

Citation: Jm. Demarchi et al., A ROBOTICS-ASSISTED PROCEDURE FOR LARGE-SCALE CYSTIC-FIBROSIS MUTATION ANALYSIS, Human mutation, 4(4), 1994, pp. 281-290

Authors: DEMARCHI JM BEAUDET AL CASKEY CT RICHARDS CS

Citation: Jm. Demarchi et al., EXPERIENCE OF AN ACADEMIC REFERENCE LABORATORY USING AUTOMATION FOR ANALYSIS OF CYSTIC-FIBROSIS MUTATIONS, Archives of pathology and laboratory medicine, 118(1), 1994, pp. 26-32

Authors: DEMARCHI JM CASKEY CT RICHARDS CS

Citation: Jm. Demarchi et al., A SINGLE AUTOMATED DNA MUTATION ASSAY FOR 3 DISEASES FREQUENT IN THE ASHKENAZIC JEWISH POPULATION, American journal of human genetics, 53(3), 1993, pp. 1483-1483