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Refinado por: Nome da Publicação: American Journal Of Human Genetics remover assunto: Biological And Medical Sciences remover
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1
Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514
Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514
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Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514

WRIGHT, A. F ; BHATTACHARYA, S. S ; CLAYTON, J. F ; DEMPSTER, M ; TIPPETT, P ; MCKEOWN, C. M. E ; JAY, M ; JAY, B ; BIRD, A. C

American journal of human genetics, 1987, Vol.41 (4), p.635-644 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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2
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints
The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints
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The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints

FAIN, P. R ; WRIGHT, E ; WILLARD, H. F ; STEPHENS, K ; BARKER, D. F

American journal of human genetics, 1989, Vol.44 (1), p.68-72 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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3
Refined physical and genetic mapping of the NFI region on chromosome 17
Refined physical and genetic mapping of the NFI region on chromosome 17
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Refined physical and genetic mapping of the NFI region on chromosome 17

FAIN, P. R ; GOLDGAR, D. E ; WALLACE, M. R ; COLLINS, F. S ; WRIGHT, E ; NGUYEN, K ; BARKER, D. F

American journal of human genetics, 1989-11, Vol.45 (5), p.721-728 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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4
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity
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Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another : confirmation of genetic heterogeneity

LESTER, D. H ; INGLEHEARN, C. F ; BASHIR, R ; ACKFORD, H ; ESAKOWITZ, L ; JAY, M ; BIRD, A. C ; WRIGHT, A. F ; PAPIHA, S. S ; BHATTACHARYA, S. S

American journal of human genetics, 1990-09, Vol.47 (3), p.536-541 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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5
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases
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Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases

CREMERS, F. P. M ; SANKILA, E.-M ; DE LA CHAPELLE, A ; PAWLOWITZKI, I. H ; ROPERS, H.-H ; BRUNSMANN, F ; JAY, M ; JAY, B ; WRIGHT, A ; PINCKERS, A. J. L. G ; SCHWARTZ, M ; VAN DE POL, D. J. R ; WIERINGA, B

American journal of human genetics, 1990-10, Vol.47 (4), p.622-628 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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6
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families
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Heterogeneity analysis in 40 X-linked retinitis pigmentosa families

TEAGUE, P. W ; ALDRED, M. A ; BUNDEY, S ; JAY, B ; BIRD, A. C ; BHATTACHARYA, S. S ; WRIGHT, A. F ; JAY, M ; DEMPSTER, M ; HARRISON, C ; CAROTHERS, A. D ; HARDWICK, L. J ; EVANS, H. J ; STRAIN, L ; BROCK, D. J. H

American journal of human genetics, 1994-07, Vol.55 (1), p.105-111 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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7
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)
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Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)

SNAREY, A ; THOMAS, S ; FRISCHAUF, A.-M ; SCHNEIDER, M. C ; POUND, S. E ; BARTON, N ; WRIGHT, A. F ; SOMLO, S ; GERMINO, G. G ; HARRIS, P. C ; REEDERS, S. T

American journal of human genetics, 1994-08, Vol.55 (2), p.365-371 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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8
Evidence for mendelian inheritance of serum IgE levels in hispanic and non-hispanic white families
Evidence for mendelian inheritance of serum IgE levels in hispanic and non-hispanic white families
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Evidence for mendelian inheritance of serum IgE levels in hispanic and non-hispanic white families

MARTINEZ, F. D ; HOLBERG, C. J ; HALONEN, M ; MORGAN, W. J ; WRIGHT, A. L ; TAUSSIG, L. M

American journal of human genetics, 1994-09, Vol.55 (3), p.555-565 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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9
Delivery of molecular genetic services within a health care system : time analysis of the clinical workload
Delivery of molecular genetic services within a health care system : time analysis of the clinical workload
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Delivery of molecular genetic services within a health care system : time analysis of the clinical workload

SURH, L. C ; WRIGHT, P. G ; CAPPELLI, M ; KASABOSKI, A ; HASTINGS, V. A ; HUNTER, A. G

American journal of human genetics, 1995-03, Vol.56 (3), p.760-768 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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10
A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3
A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3
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A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3

FUJITA, R ; BINGHAM, E ; WRIGHT, A. F ; OTT, J ; SIEVING, P. A ; SWAROOP, A ; FORSYTHE, P ; MCHENRY, C ; AITA, V ; NAVIA, B. A ; DRY, K ; SEGAL, M ; DEVOTO, M ; BRUNS, G

American journal of human genetics, 1996-07, Vol.59 (1), p.152-158 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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