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MATISE TC
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Citation: H. Kobayashi et al., TOWARDS FULLY AUTOMATED GENOTYPING - USE OF AN X-LINKED RECESSIVE SPASTIC PARAPLEGIA FAMILY TO TEST ALTERNATIVE ANALYSIS-METHODS, Human genetics, 95(5), 1995, pp. 483-490
Citation: Tc. Matise et A. Chakravarti, AUTOMATED CONSTRUCTION OF RADIATION HYBRID MAPS USING MULTIMAP, American journal of human genetics, 57(4), 1995, pp. 68-68
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Citation: H. Kobayashi et al., A GENE FOR X-LINKED INFANTILE SPINAL MUSCULAR-ATROPHY (A SEVERE LETHAL FORM OF X-LINKED ARTHROGRYPOSIS) MAPS TO XP11.3-Q11.2, American journal of human genetics, 57(4), 1995, pp. 1881-1881
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Citation: Yy. Shugart et al., FINE GENETIC-MAPPING OF A GENE FOR AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA ON CHROMOSOME 6P21, American journal of human genetics, 57(2), 1995, pp. 499-502
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Citation: Tc. Matise et al., AUTOMATED CONSTRUCTION OF GENETIC-LINKAGE MAPS USING AN EXPERT-SYSTEM(MULTIMAP) - A HUMAN GENOME LINKAGE MAP (VOL 6, PG 384, 1994), Nature genetics, 7(2), 1994, pp. 215-215
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Citation: Eg. Puffenberger et al., IDENTITY-BY-DESCENT AND ASSOCIATION MAPPING OF A RECESSIVE GENE FOR HIRSCHSPRUNG DISEASE ON HUMAN-CHROMOSOME 13Q22, Human molecular genetics, 3(8), 1994, pp. 1217-1225
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Citation: Dn. Finegold et al., PRELIMINARY LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM TO CHROMOSOME 3Q13, Pediatric research, 36(3), 1994, pp. 414-417
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PATEL PI
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Citation: Tc. Matise et al., DETECTION OF TANDEM DUPLICATIONS AND IMPLICATIONS FOR LINKAGE ANALYSIS, American journal of human genetics, 54(6), 1994, pp. 1110-1121
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Citation: M. Angrist et al., A GENE FOR HIRSCHSPRUNG DISEASE (MEGACOLON) IN THE PERICENTROMERIC REGION OF HUMAN CHROMOSOME-10, Nature genetics, 4(4), 1993, pp. 351-356
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Citation: Mg. Mcinnis et al., A LINKAGE MAP OF HUMAN CHROMOSOME-21 - 43 PCR MARKERS AT AVERAGE INTERVALS OF 2.5 CM, Genomics, 16(3), 1993, pp. 562-571
Citation: Tc. Matise et De. Weeks, DETECTING HETEROGENEITY WITH THE AFFECTED-PEDIGREE-MEMBER (APM) METHOD, Genetic epidemiology, 10(6), 1993, pp. 401-406
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Citation: M. Angrist et al., A GENETIC-LOCUS FOR HIRSCHSPRUNG DISEASE IN THE PERICENTROMERIC REGION OF CHROMOSOME-10, American journal of human genetics, 53(3), 1993, pp. 134-134
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MATISE TC
BLASCHAK JE
KOMPANEK AJ
WEEKS DE
CHAKRAVARTI A
Citation: Tc. Matise et al., PATTERNS OF SEX-DIFFERENCE AND INTERFERENCE IN THE HUMAN GENOME, American journal of human genetics, 53(3), 1993, pp. 262-262
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PUFFENBERGER EG
KAUFFMAN ER
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MATISE TC
CHAKRAVARTI A
Citation: Eg. Puffenberger et al., IDENTITY-BY-DESCENT MAPPING OF HIRSCHSPRUNG DISEASE IN A LARGE MENNONITE KINDRED, American journal of human genetics, 53(3), 1993, pp. 1062-1062
Citation: De. Weeks et al., DETECTION OF TANDEMLY DUPLICATED GENETIC-MARKERS AND IMPLICATIONS FORLINKAGE ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 1100-1100