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Results:
1-13
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Results: 13
Authors:
Blanco, P
Sargent, CA
Boucher, CA
Howell, G
Ross, M
Affara, NA
Citation: P. Blanco et al., A novel poly(A)-binding protein gene (PABPC5) maps to an X-specific subinterval in the Xq21.3/Yp11.2 homology block of the human sex chromosomes, GENOMICS, 74(1), 2001, pp. 1-11
Authors:
Sargent, CA
Boucher, CA
Blanco, P
Chalmers, IJ
Highet, L
Hall, N
Ross, N
Crow, T
Affara, NA
Citation: Ca. Sargent et al., Characterization of the human Xq21.3/Yp11 homology block and conservation of organization in primates, GENOMICS, 73(1), 2001, pp. 77-85
Authors:
Boucher, CA
Sargent, CA
Ogata, T
Affara, NA
Citation: Ca. Boucher et al., Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location, J MED GENET, 38(9), 2001, pp. 591-598
Authors:
Ross, NLJ
Yang, J
Sargent, CA
Boucher, CA
Nanko, S
Wadekar, R
Williams, NA
Affara, NA
Ross, NLJ
Citation: Nlj. Ross et al., Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X,t(X;Y)(p22.33;p11.2) male with schizophrenia, J MED GENET, 38(10), 2001, pp. 710-719
Authors:
Blanco, P
Sargent, CA
Boucher, CA
Mitchell, M
Affara, NA
Citation: P. Blanco et al., Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain, MAMM GENOME, 11(10), 2000, pp. 906-914
Authors:
Woodward, ER
Buchberger, A
Clifford, SC
Hurst, LD
Affara, NA
Maher, ER
Citation: Er. Woodward et al., Comparative sequence analysis of the VHL tumor suppressor gene, GENOMICS, 65(3), 2000, pp. 253-265
Authors:
Affara, NA
Mitchell, MJ
Citation: Na. Affara et Mj. Mitchell, The role of human and mouse Y chromosome genes in male infertility, J ENDOC INV, 23(10), 2000, pp. 630-645
Authors:
Sargent, CA
Kidd, A
Moore, S
Dean, J
Besley, GTN
Affara, NA
Citation: Ca. Sargent et al., Five cases of isolated glycerol kinase deficiency, including two families:failure to find genotype : phenotype correlation, J MED GENET, 37(6), 2000, pp. 434-441
Authors:
Woodward, ER
Clifford, SC
Astuti, D
Affara, NA
Maher, ER
Citation: Er. Woodward et al., Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes, J MED GENET, 37(5), 2000, pp. 348-353
Authors:
Wong, J
Blanco, P
Affara, NA
Citation: J. Wong et al., An exon map of the AZFc male infertility region of the human Y Chromosome, MAMM GENOME, 10(1), 1999, pp. 57-61
Authors:
Bartoloni, L
Blouin, JLC
Sainsbury, AJ
Gos, A
Morris, MA
Affara, NA
DeLozier-Blanchet, CD
Antonarakis, SE
Citation: L. Bartoloni et al., Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping, CYTOG C GEN, 84(3-4), 1999, pp. 188-189
Authors:
Sargent, CA
Boucher, CA
Kirsch, S
Brown, G
Weiss, B
Trundley, A
Burgoyne, P
Saut, N
Durand, C
Levy, N
Terriou, P
Hargreave, T
Cooke, H
Mitchell, M
Rappold, GA
Affara, NA
Citation: Ca. Sargent et al., The critical region of overlap defining the AZFa male infertility intervalof proximal Yq contains three transcribed sequences, J MED GENET, 36(9), 1999, pp. 670-677
Authors:
Jobling, MA
Williams, G
Schiebel, K
Pandya, A
McElreavey, K
Salas, L
Rappold, GA
Affara, NA
Tyler-Smith, C
Citation: Ma. Jobling et al., A selective difference between human Y-chromosomal DNA haplotypes, CURR BIOL, 8(25), 1998, pp. 1391-1394
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1-13
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