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Results: 1-10 |
Results: 10
GAUCHER TYPE-2 DISEASE - IDENTIFICATION OF A NOVEL TRANSVERSION MUTATION IN A FRENCH-IRISH PATIENT
Authors: CHOY FYM HUMPHRIES ML BENYOSEPH Y
Citation: Fym. Choy et al., GAUCHER TYPE-2 DISEASE - IDENTIFICATION OF A NOVEL TRANSVERSION MUTATION IN A FRENCH-IRISH PATIENT, American journal of medical genetics, 78(1), 1998, pp. 92-93
AN ALTERNATIVE WAY TO DIAGNOSE BCR-ABL BY PCR
Authors: VO T PINDER H BENYOSEPH Y FELDMAN G
Citation: T. Vo et al., AN ALTERNATIVE WAY TO DIAGNOSE BCR-ABL BY PCR, The American journal of pathology, 151(5), 1997, pp. 6-6
IMPROVEMENT OF BIOCHEMICAL TESTING FOR CARRIERS OF TAY-SACHS-DISEASE BY MOLECULAR TESTING OF INCONCLUSIVE SPECIMENS
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, IMPROVEMENT OF BIOCHEMICAL TESTING FOR CARRIERS OF TAY-SACHS-DISEASE BY MOLECULAR TESTING OF INCONCLUSIVE SPECIMENS, American journal of human genetics, 61(4), 1997, pp. 2305-2305
DETECTION OF FARBER-DISEASE BY RADIOSCANNING CERAMIDASE ASSAYS
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, DETECTION OF FARBER-DISEASE BY RADIOSCANNING CERAMIDASE ASSAYS, Journal of investigative medicine, 44(7), 1996, pp. 368-368
DISCRIMINATION BETWEEN METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE-A BY RESTRICTION DIGEST OF AMPLIFIED GENE FRAGMENTS
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, DISCRIMINATION BETWEEN METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE-A BY RESTRICTION DIGEST OF AMPLIFIED GENE FRAGMENTS, The American journal of the medical sciences, 309(2), 1995, pp. 88-91
DETECTION OF INDIVIDUAL GLYCOSYLATION AND POLYADENYLATION MUTATIONS CAUSING PSEUDO-DEFICIENCY OF ARYLSULFATASE A BY ALLELE-SPECIFIC AMPLIFICATION AND BY RESTRICTION DIGEST
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, DETECTION OF INDIVIDUAL GLYCOSYLATION AND POLYADENYLATION MUTATIONS CAUSING PSEUDO-DEFICIENCY OF ARYLSULFATASE A BY ALLELE-SPECIFIC AMPLIFICATION AND BY RESTRICTION DIGEST, Pediatric research, 35(4), 1994, pp. 10000156-10000156
DETECTION OF INDIVIDUAL AND CONCURRENT GLYCOSYLATION AND POLYADENYLATION MUTATIONS CAUSING PSEUDODEFICIENCY OF ARYLSULFATASE-A
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, DETECTION OF INDIVIDUAL AND CONCURRENT GLYCOSYLATION AND POLYADENYLATION MUTATIONS CAUSING PSEUDODEFICIENCY OF ARYLSULFATASE-A, Clinical research, 42(3), 1994, pp. 10000434-10000434
RAPID DETECTION OF COMMON METACHROMATIC LEUKODYSTROPHY MUTATIONS BY RESTRICTION ANALYSIS OF ARYLSULFATASE-A GENE AMPLIMERS
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, RAPID DETECTION OF COMMON METACHROMATIC LEUKODYSTROPHY MUTATIONS BY RESTRICTION ANALYSIS OF ARYLSULFATASE-A GENE AMPLIMERS, Clinica chimica acta, 226(1), 1994, pp. 77-82
DISCRIMINATION BETWEEN METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE A BY RESTRICTION DIGEST OF AMPLIFIED GENE FRAGMENTS
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, DISCRIMINATION BETWEEN METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE A BY RESTRICTION DIGEST OF AMPLIFIED GENE FRAGMENTS, Clinical research, 41(3), 1993, pp. 10000692-10000692
RAPID MOLECULAR DIAGNOSIS OF MUTATIONS CAUSING METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE-A
Authors: BENYOSEPH Y MITCHELL DA
Citation: Y. Benyoseph et Da. Mitchell, RAPID MOLECULAR DIAGNOSIS OF MUTATIONS CAUSING METACHROMATIC LEUKODYSTROPHY AND PSEUDO-DEFICIENCY OF ARYLSULFATASE-A, American journal of human genetics, 53(3), 1993, pp. 890-890
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