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Results: 1-25 | 26-50 | 51-59 |
Results: 51-59/59
REFINED ASSIGNMENT OF THE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS (INCL, CLN1) LOCUS AT 1P32 - INCORPORATION OF LINKAGE DISEQUILIBRIUM IN MULTIPOINT ANALYSIS
Authors: HELLSTEN E VESA J SPEER MC MAKELA TP JARVELA I ALITALO K OTT J PELTONEN L
Citation: E. Hellsten et al., REFINED ASSIGNMENT OF THE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS (INCL, CLN1) LOCUS AT 1P32 - INCORPORATION OF LINKAGE DISEQUILIBRIUM IN MULTIPOINT ANALYSIS, Genomics, 16(3), 1993, pp. 720-725
FLANKING MARKERS DEFINE THE X-LINKED HYPOPHOSPHATEMIC RICKETS GENE LOCUS
Authors: ECONS MJ FAIN PR NORMAN M SPEER MC PERICAKVANCE MA BECKER PA BARKER DF TAYLOR A DREZNER MK
Citation: Mj. Econs et al., FLANKING MARKERS DEFINE THE X-LINKED HYPOPHOSPHATEMIC RICKETS GENE LOCUS, Journal of bone and mineral research, 8(9), 1993, pp. 1149-1152
FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE
Authors: ECONS MJ ROWE PSN FRANCIS F BARKER DF SPEER MC NORMAN M PERICAKVANCE MA FAIN PR WEISSENBACH J READ A BECKER PA LEHRACH H ORIORDAN J DREZNER MK
Citation: Mj. Econs et al., FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE, Journal of bone and mineral research, 8, 1993, pp. 190000137-190000137
GERMLINE VERSUS SOMATIC DIVERSITY OF THE P(CTG)N REPEAT IN MYOTONIC-DYSTROPHY
Authors: TAYLOR HP SCHWARTZBACH CJ GILBERT JR KOZATAYLOR PH SPEER MC STAJICH JM PERICAKVANCE MA ROSES AD
Citation: Hp. Taylor et al., GERMLINE VERSUS SOMATIC DIVERSITY OF THE P(CTG)N REPEAT IN MYOTONIC-DYSTROPHY, Neurology, 43(4), 1993, pp. 280-280
EVIDENCE FOR GENETIC-HETEROGENEITY IN THE DOMINANT FORM OF LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: SPEER MC YAMAOKA LH GILCHRIST JM WESTBROOK C STAJICH JM GASKELL PC ROSES AD PERICAKVANCE MA
Citation: Mc. Speer et al., EVIDENCE FOR GENETIC-HETEROGENEITY IN THE DOMINANT FORM OF LIMB-GIRDLE MUSCULAR-DYSTROPHY, American journal of human genetics, 53(3), 1993, pp. 1082-1082
AUTOSOMAL-DOMINANT MUSCULAR-DYSTROPHY (LGM1) - A GENETIC-MAP OF CHROMOSOME 5Q31 AND REFINING THE LOCATION OF LGM1 BY MULTIPOINT ANALYSIS
Authors: YAMAOKA LH WESTBROOK CA SPEER MC GILCHRIST JM JABS EW STAJICH JM GASKELL CP ROSES AD PERICAKVANCE MA
Citation: Lh. Yamaoka et al., AUTOSOMAL-DOMINANT MUSCULAR-DYSTROPHY (LGM1) - A GENETIC-MAP OF CHROMOSOME 5Q31 AND REFINING THE LOCATION OF LGM1 BY MULTIPOINT ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 1110-1110
MYOTONIC-DYSTROPHY IN AN AFFECTED FAMILY MEMBER INHERITING AFFECTED PARENTS NORMAL CHROMOSOME
Authors: TAYLOR HP SCHWARTZBACH CJ GILBERT JR KOZATAYLOR PH SPEER MC STAJICH JM KRAHE R SICILIANO MJ ROSES AD
Citation: Hp. Taylor et al., MYOTONIC-DYSTROPHY IN AN AFFECTED FAMILY MEMBER INHERITING AFFECTED PARENTS NORMAL CHROMOSOME, American journal of human genetics, 53(3), 1993, pp. 1238-1238
LINKAGE ANALYSIS IN AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: GILCHRIST JM JACKSON C BECKMANN J DONALD L WALSH K SPEER MC PERICAKVANCE MA
Citation: Jm. Gilchrist et al., LINKAGE ANALYSIS IN AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY, American journal of human genetics, 53(3), 1993, pp. 1694-1694
EVIDENCE FOR HETEROGENEITY IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)
Authors: GILBERT JR STAJICH JM WALL S CARTER SC QIU H VANCE JM STEWART CS SPEER MC PUFKY J YAMAOKA LH ROZEAR M SAMSON F FARDEAU M ROSES AD PERICAKVANCE MA
Citation: Jr. Gilbert et al., EVIDENCE FOR HETEROGENEITY IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), American journal of human genetics, 53(2), 1993, pp. 401-408
Risultati: 1-25 | 26-50 | 51-59 |