AAAAAA

   
Results: 1-18 |
Results: 18
EXPRESSION OF MESSENGER-RNA FOR TYPE-IV COLLAGEN ALPHA-1, ALPHA-5 ANDALPHA-6 CHAINS BY CULTURED DERMAL FIBROBLASTS FROM PATIENTS WITH X-LINKED ALPORT-SYNDROME
Authors: SASAKI S ZHOU B FAN WW BARKER DF DENISON JC ATKIN CL GREGORY MC ZHOU J SEGAL Y SADO Y NINOMIYA Y MICHAEL AF KASHTAN CE
Citation: S. Sasaki et al., EXPRESSION OF MESSENGER-RNA FOR TYPE-IV COLLAGEN ALPHA-1, ALPHA-5 ANDALPHA-6 CHAINS BY CULTURED DERMAL FIBROBLASTS FROM PATIENTS WITH X-LINKED ALPORT-SYNDROME, Matrix biology, 17(4), 1998, pp. 279-291
PARENTAL ORIGIN-DEPENDENT, MALE OFFSPRING-SPECIFIC TRANSMISSION-RATIODISTORTION AT LOCI ON THE HUMAN X-CHROMOSOME
Authors: NAUMOVA AK LEPPERT M BARKER DF MORGAN K SAPIENZA C
Citation: Ak. Naumova et al., PARENTAL ORIGIN-DEPENDENT, MALE OFFSPRING-SPECIFIC TRANSMISSION-RATIODISTORTION AT LOCI ON THE HUMAN X-CHROMOSOME, American journal of human genetics, 62(6), 1998, pp. 1493-1499
COMMON ANCESTRY OF 3 ASHKENAZI-AMERICAN FAMILIES WITH ALPORT-SYNDROMEAND COL4A5 R1677Q
Authors: BARKER DF DENISON JC ATKIN CL GREGORY MC
Citation: Df. Barker et al., COMMON ANCESTRY OF 3 ASHKENAZI-AMERICAN FAMILIES WITH ALPORT-SYNDROMEAND COL4A5 R1677Q, Human genetics, 99(5), 1997, pp. 681-684
THE BRCA1 AND 1A1.3B PROMOTERS ARE PARALLEL ELEMENTS OF A GENOMIC DUPLICATION AT 17Q21
Authors: BARKER DF LIU XD ALMEIDA ERA
Citation: Df. Barker et al., THE BRCA1 AND 1A1.3B PROMOTERS ARE PARALLEL ELEMENTS OF A GENOMIC DUPLICATION AT 17Q21, Genomics, 38(2), 1996, pp. 215-222
BRCA1 R841W - A STRONG CANDIDATE FOR A COMMON MUTATION WITH MODERATE PHENOTYPE
Authors: BARKER DF ALMEIDA ERA CASEY G FAIN PR LIAO SY MASUNAKA I NOBLE B KUROSAKI T ANTONCULVER H
Citation: Df. Barker et al., BRCA1 R841W - A STRONG CANDIDATE FOR A COMMON MUTATION WITH MODERATE PHENOTYPE, Genetic epidemiology, 13(6), 1996, pp. 595-604
REFINED GENETIC-MAPPING AND PROTEOLIPID PROTEIN MUTATION ANALYSIS IN X-LINKED PURE HEREDITARY SPASTIC PARAPLEGIA
Authors: CAMBI F TANG XM CORDRAY P FAIN PR KEPPEN LD BARKER DF
Citation: F. Cambi et al., REFINED GENETIC-MAPPING AND PROTEOLIPID PROTEIN MUTATION ANALYSIS IN X-LINKED PURE HEREDITARY SPASTIC PARAPLEGIA, Neurology, 46(4), 1996, pp. 1112-1117
A MUTATION CAUSING ALPORT SYNDROME WITH TARDIVE HEARING-LOSS IS COMMON IN THE WESTERN UNITED-STATES
Authors: BARKER DF PRUCHNO CJ JIANG X ATKIN CL STONE EM DENISON LC FAIN PR GREGORY MC
Citation: Df. Barker et al., A MUTATION CAUSING ALPORT SYNDROME WITH TARDIVE HEARING-LOSS IS COMMON IN THE WESTERN UNITED-STATES, American journal of human genetics, 58(6), 1996, pp. 1157-1165
A 2D CROSSOVER-BASED MAP OF THE HUMAN X-CHROMOSOME AS A MODEL FOR MAPINTEGRATION
Authors: FAIN PR KORT EN CHANCE PF NGUYEN K REDD DF ECONS MJ BARKER DF
Citation: Pr. Fain et al., A 2D CROSSOVER-BASED MAP OF THE HUMAN X-CHROMOSOME AS A MODEL FOR MAPINTEGRATION, Nature genetics, 9(3), 1995, pp. 261-266
CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1
Authors: PERICAKVANCE MA BARKER DF BERGOFFEN JA CHANCE P COCHRANE S DAHL N EXLER MC FAIN PR FAIRWEATHER ND FISCHBECK K GAL A HAITES N IONASESCU R IONASESCU VV KENNERSON ML MONACO AP MOSTACCUIOLO M NICHOLSON GA SILLEN A HAINES JL
Citation: Ma. Pericakvance et al., CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1, Human heredity, 45(3), 1995, pp. 121-128
THE SAME POLYMORPHISM IDENTIFIED BY THE DXS571(B) AND DXS1105 LOCI
Authors: BARKER DF CORDRAY P FAIN PR
Citation: Df. Barker et al., THE SAME POLYMORPHISM IDENTIFIED BY THE DXS571(B) AND DXS1105 LOCI, Human molecular genetics, 3(10), 1994, pp. 1913-1913
HEARING-LOSS
Authors: GREGORY MC ATKINS CL BARKER DF
Citation: Mc. Gregory et al., HEARING-LOSS, The New England journal of medicine, 330(10), 1994, pp. 714-714
FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE LOCUS
Authors: ECONS MJ ROWE PSN FRANCIS F BARKER DF SPEER MC NORMAN M PAIN PR WEISSENBACH J READ A DAVIS KE BECKER PA LEHRACH H ORIORDAN J DREZNER MK
Citation: Mj. Econs et al., FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE LOCUS, The Journal of clinical endocrinology and metabolism, 79(5), 1994, pp. 1351-1354
REFINED GENETIC-MAPPING OF X-LINKED CHARCOT-MARIE-TOOTH NEUROPATHY
Authors: FAIN PR BARKER DF CHANCE PF
Citation: Pr. Fain et al., REFINED GENETIC-MAPPING OF X-LINKED CHARCOT-MARIE-TOOTH NEUROPATHY, American journal of human genetics, 54(2), 1994, pp. 229-235
2 SIMPLE REPEAT POLYMORPHISMS AT DXS337
Authors: BARKER DF NGUYEN K FAIN PR
Citation: Df. Barker et al., 2 SIMPLE REPEAT POLYMORPHISMS AT DXS337, Human molecular genetics, 2(9), 1993, pp. 1507-1507
A CA DINUCLEOTIDE POLYMORPHISM AT D17S107 (17Q12-Q24)
Authors: BARKER DF NGUYEN K FAIN PR
Citation: Df. Barker et al., A CA DINUCLEOTIDE POLYMORPHISM AT D17S107 (17Q12-Q24), Human molecular genetics, 2(7), 1993, pp. 1086-1086
DEFINITION AND MAPPING OF STSS AT STR AND RFLP LOCI IN XP11-XQ22
Authors: BARKER DF FAIN PR
Citation: Df. Barker et Pr. Fain, DEFINITION AND MAPPING OF STSS AT STR AND RFLP LOCI IN XP11-XQ22, Genomics, 18(3), 1993, pp. 712-716
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
Risultati: 1-18 |