-
1
-
-
0002129691
-
Systemic sclerosis (scleroderma), localized forms of scleroderma, and calcinosis
-
McCarty DJ, Koopman WJ, editors. Philadelphia: Lea and Febiger
-
Medsger TA Jr. Systemic sclerosis (scleroderma), localized forms of scleroderma, and calcinosis. In: McCarty DJ, Koopman WJ, editors. Arthritis and allied conditions. Philadelphia: Lea and Febiger; 1993. p. 1253-99.
-
(1993)
Arthritis and Allied Conditions
, pp. 1253-1299
-
-
Medsger Jr., T.A.1
-
2
-
-
0025841639
-
Epidemiology of scleroderma
-
Silman A. Epidemiology of scleroderma. Curr Opin Rheumatol 1991;3:967-72.
-
(1991)
Curr Opin Rheumatol
, vol.3
, pp. 967-972
-
-
Silman, A.1
-
3
-
-
0029199990
-
HLA and autoimmunity in scleroderma (systemic sclerosis)
-
Arnett FC. HLA and autoimmunity in scleroderma (systemic sclerosis). Int Rev Immunol 1995;12:107-28.
-
(1995)
Int Rev Immunol
, vol.12
, pp. 107-128
-
-
Arnett, F.C.1
-
4
-
-
0026697010
-
Association of polar amino acid sequences at position 26 of the HLA-DQB1 first domain with the anti-centromere autoantibody response in systemic sclerosis (scleroderma)
-
Reveille JD, Owerbach D, Goldstein R, Moreda R, Isern RA, Arnett FC. Association of polar amino acid sequences at position 26 of the HLA-DQB1 first domain with the anti-centromere autoantibody response in systemic sclerosis (scleroderma). J Clin Invest 1992;89:1208-13.
-
(1992)
J Clin Invest
, vol.89
, pp. 1208-1213
-
-
Reveille, J.D.1
Owerbach, D.2
Goldstein, R.3
Moreda, R.4
Isern, R.A.5
Arnett, F.C.6
-
5
-
-
0026669338
-
Association of amino acid sequences in the HLA-DQB1 first domain with the anti-topoisomerase I autoantibody response in scleroderma (progressive systemic sclerosis)
-
Reveille JD, Durban E, MacLeod-St. Clair MJ, Goldstein R, Moreda R, Altman RD, et al. Association of amino acid sequences in the HLA-DQB1 first domain with the anti-topoisomerase I autoantibody response in scleroderma (progressive systemic sclerosis). J Clin Invest 1992;90:973-80.
-
(1992)
J Clin Invest
, vol.90
, pp. 973-980
-
-
Reveille, J.D.1
Durban, E.2
MacLeod-St. Clair, M.J.3
Goldstein, R.4
Moreda, R.5
Altman, R.D.6
-
6
-
-
0027291530
-
The HLA-DR and DQ genes control the autoimmune response to DNA topoisomerase I in systemic sclerosis (scleroderma)
-
Kuwana M, Kaburaki J, Okano Y, Inoko H, Tsuj K. The HLA-DR and DQ genes control the autoimmune response to DNA topoisomerase I in systemic sclerosis (scleroderma). J Clin Invest 1993;92:1296-301.
-
(1993)
J Clin Invest
, vol.92
, pp. 1296-1301
-
-
Kuwana, M.1
Kaburaki, J.2
Okano, Y.3
Inoko, H.4
Tsuj, K.5
-
7
-
-
0030015175
-
Autoantibodies to fibrillarin in systemic sclerosis (scleroderma): An immunogenetic, serologic, and clinical analysis
-
Arnett FC, Reveille JD, Goldstein R, Pollard KM, Leaird K, Smith EA, et al. Autoantibodies to fibrillarin in systemic sclerosis (scleroderma): an immunogenetic, serologic, and clinical analysis. Arthritis Rheum 1996;39:1151-60.
-
(1996)
Arthritis Rheum
, vol.39
, pp. 1151-1160
-
-
Arnett, F.C.1
Reveille, J.D.2
Goldstein, R.3
Pollard, K.M.4
Leaird, K.5
Smith, E.A.6
-
8
-
-
0023942434
-
Familial clustering of scleroderma spectrum disease
-
McGregor AR, Watson A, Yunis E, Pandey JP, Takehara K, Tidwell JT, et al. Familial clustering of scleroderma spectrum disease. Am J Med 1988;84:1023-32.
-
(1988)
Am J Med
, vol.84
, pp. 1023-1032
-
-
McGregor, A.R.1
Watson, A.2
Yunis, E.3
Pandey, J.P.4
Takehara, K.5
Tidwell, J.T.6
-
9
-
-
0028850792
-
Immunogenetic analysis of 5 families with multicase occurrence of scleroderma and/or related variants
-
Manolios N, Dunckley H, Chivers T, Brooks P, Englert H. Immunogenetic analysis of 5 families with multicase occurrence of scleroderma and/or related variants. J Rheumatol 1995;22:85-92.
-
(1995)
J Rheumatol
, vol.22
, pp. 85-92
-
-
Manolios, N.1
Dunckley, H.2
Chivers, T.3
Brooks, P.4
Englert, H.5
-
10
-
-
0028556496
-
Familial scleroderma - Evidence for environmental versus genetic trigger
-
Stephens CO, Briggs DC, Whyte J, Artlett CM, Scherbakov AB, Olsen N, et al. Familial scleroderma - evidence for environmental versus genetic trigger. Br J Rheumatol 1994;33:1131-5.
-
(1994)
Br J Rheumatol
, vol.33
, pp. 1131-1135
-
-
Stephens, C.O.1
Briggs, D.C.2
Whyte, J.3
Artlett, C.M.4
Scherbakov, A.B.5
Olsen, N.6
-
11
-
-
0029982537
-
Genetic analysis of autoimmune disease
-
Vyse TJ, Todd JA. Genetic analysis of autoimmune disease. Cell 1996;85:311-8.
-
(1996)
Cell
, vol.85
, pp. 311-318
-
-
Vyse, T.J.1
Todd, J.A.2
-
12
-
-
0029563530
-
Segregation of autoantibodies with disease in monozygotic twin pairs discordant for systemic sclerosis: Three further cases
-
McHugh NJ, Harvey GR, Whyte J, Dorsey JK. Segregation of autoantibodies with disease in monozygotic twin pairs discordant for systemic sclerosis: three further cases. Arthritis Rheum 1995; 38:1845-50.
-
(1995)
Arthritis Rheum
, vol.38
, pp. 1845-1850
-
-
McHugh, N.J.1
Harvey, G.R.2
Whyte, J.3
Dorsey, J.K.4
-
13
-
-
0027508153
-
Features of systemic sclerosis (scleroderma) in an identical twin pair
-
Cook NJ, Silman AJ, Propert J, Cawley MID. Features of systemic sclerosis (scleroderma) in an identical twin pair. Br J Rheumatol 1993;32:926-8.
-
(1993)
Br J Rheumatol
, vol.32
, pp. 926-928
-
-
Cook, N.J.1
Silman, A.J.2
Propert, J.3
Cawley, M.I.D.4
-
15
-
-
0020160884
-
Scleroderma in 5 year old twin girls
-
Zorina VJ, Zorin SP. Scleroderma in 5 year old twin girls. Pediatriya 1982;7:69-70.
-
(1982)
Pediatriya
, vol.7
, pp. 69-70
-
-
Zorina, V.J.1
Zorin, S.P.2
-
16
-
-
0015059119
-
Progressive systemic sclerosis and localized scleroderma (morphea) with positive LE cell test and unusual systemic manifestations compatible with systemic lupus erythematosus: Presentation of 14 cases including one set of identical twins, one with scleroderma and the other with SLE
-
Baltimore
-
Dubois EL, Chandor S, Friou G, Bischel M. Progressive systemic sclerosis and localized scleroderma (morphea) with positive LE cell test and unusual systemic manifestations compatible with systemic lupus erythematosus: presentation of 14 cases including one set of identical twins, one with scleroderma and the other with SLE. Medicine (Baltimore) 1971;50:199-222.
-
(1971)
Medicine
, vol.50
, pp. 199-222
-
-
Dubois, E.L.1
Chandor, S.2
Friou, G.3
Bischel, M.4
-
18
-
-
0028533483
-
Of mice and Marfan: Genetic linkage analyses of the fibrillin genes, FBN1 and FBN2, in the mouse genome
-
Goldstein C, Liaw P, Jimenez SA, Buchberg MA, Siracusa LD. Of mice and Marfan: genetic linkage analyses of the fibrillin genes, FBN1 and FBN2, in the mouse genome. Mamm Genome 1994;5: 696-700.
-
(1994)
Mamm Genome
, vol.5
, pp. 696-700
-
-
Goldstein, C.1
Liaw, P.2
Jimenez, S.A.3
Buchberg, M.A.4
Siracusa, L.D.5
-
19
-
-
0028086621
-
The tight-skin (tsk) mutation is closely linked to B2m on mouse chromosome 2
-
Everett ET, Pablos JL, Harris SE, Leroy EC, Norris JS. The tight-skin (tsk) mutation is closely linked to B2m on mouse chromosome 2. Mamm Genome 1994;5:55-7.
-
(1994)
Mamm Genome
, vol.5
, pp. 55-57
-
-
Everett, E.T.1
Pablos, J.L.2
Harris, S.E.3
Leroy, E.C.4
Norris, J.S.5
-
20
-
-
0028048709
-
Tight-skin (TSK) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15
-
Doute RC, Clark SH. Tight-skin (TSK) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15. Genomics 1994;22:223-5.
-
(1994)
Genomics
, vol.22
, pp. 223-225
-
-
Doute, R.C.1
Clark, S.H.2
-
22
-
-
0028085306
-
A physical map of the region encompassing the human interleukin-a, interleukin-1β and interleukin-1 receptor antagonist genes
-
Nicklin M, Weith A, Duff GW. A physical map of the region encompassing the human interleukin-a, interleukin-1β and interleukin-1 receptor antagonist genes. Genomics 1994;19:382-4.
-
(1994)
Genomics
, vol.19
, pp. 382-384
-
-
Nicklin, M.1
Weith, A.2
Duff, G.W.3
-
24
-
-
0029610915
-
The tight skin 2 mouse: An animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration
-
Christner PJ, Peters J, Hawkins D, Siracusa LD, Jiménez SA. The tight skin 2 mouse: an animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration. Arthritis Rheum 1995;38:1791-8.
-
(1995)
Arthritis Rheum
, vol.38
, pp. 1791-1798
-
-
Christner, P.J.1
Peters, J.2
Hawkins, D.3
Siracusa, L.D.4
Jiménez, S.A.5
-
25
-
-
9444226445
-
Increased prevalence of systemic sclerosis in a native American tribe in Oklahoma: Association with an Amerindian HLA haplotype
-
Arnett FC, Howard RF, Tan F, Moulds JM, Bias WB, Durban E, et al. Increased prevalence of systemic sclerosis in a native American tribe in Oklahoma: association with an Amerindian HLA haplotype. Arthritis Rheum 1996;39:1362-70.
-
(1996)
Arthritis Rheum
, vol.39
, pp. 1362-1370
-
-
Arnett, F.C.1
Howard, R.F.2
Tan, F.3
Moulds, J.M.4
Bias, W.B.5
Durban, E.6
-
26
-
-
0027942323
-
Genome screening by searching for shared segments: Mapping a gene for benign recurrent intrahepatic cholestasis
-
Houwen RH, Baharloo JS, Blankenship K, Raeymaekers P, Juyn J, Sandkuijl LA, et al. Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis. Nat Genet 1994;8:380-6.
-
(1994)
Nat Genet
, vol.8
, pp. 380-386
-
-
Houwen, R.H.1
Baharloo, J.S.2
Blankenship, K.3
Raeymaekers, P.4
Juyn, J.5
Sandkuijl, L.A.6
-
27
-
-
0026949420
-
Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
-
Hastbacka J, del la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet 1992;2: 204-11.
-
(1992)
Nat Genet
, vol.2
, pp. 204-211
-
-
Hastbacka, J.1
Del La Chapelle, A.2
Kaitila, I.3
Sistonen, P.4
Weaver, A.5
Lander, E.6
-
28
-
-
0018887574
-
Preliminary criteria for the classification of systemic sclerosis (scleroderma)
-
Subcommittee for Scleroderma Criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee. Preliminary criteria for the classification of systemic sclerosis (scleroderma). Arthritis Rheum 1980;23:581-90.
-
(1980)
Arthritis Rheum
, vol.23
, pp. 581-590
-
-
-
29
-
-
0017148259
-
A general method for isolation of high molecular weight DNA from eukaryotes
-
Blin N, Stafford DW. A general method for isolation of high molecular weight DNA from eukaryotes. Nucleic Acids Res 1978;3:2303-8.
-
(1978)
Nucleic Acids Res
, vol.3
, pp. 2303-2308
-
-
Blin, N.1
Stafford, D.W.2
-
31
-
-
0025900544
-
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes
-
Lee B, Godfrey M, Vitale E, Hori H, Mattel M, Sarfarazi M, et al. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 1991;352:330-4.
-
(1991)
Nature
, vol.352
, pp. 330-334
-
-
Lee, B.1
Godfrey, M.2
Vitale, E.3
Hori, H.4
Mattel, M.5
Sarfarazi, M.6
-
32
-
-
0028292451
-
A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome
-
Pereira L, Levran O, Ramirez F, Lynch JR, Sykes B, Pyeritz RE, et al. A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome. N Engl J Med 1994;331: 148-53.
-
(1994)
N Engl J Med
, vol.331
, pp. 148-153
-
-
Pereira, L.1
Levran, O.2
Ramirez, F.3
Lynch, J.R.4
Sykes, B.5
Pyeritz, R.E.6
-
33
-
-
0027532002
-
A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1
-
Barber TD, Morell R, Johnson DH, Asher JH Jr, Friedman TB. A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1. Hum Mol Genet 1993;2:88.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 88
-
-
Barber, T.D.1
Morell, R.2
Johnson, D.H.3
Asher Jr., J.H.4
Friedman, T.B.5
-
34
-
-
0027968267
-
Dinucleotide repeat polymorphism in the human IL1A gene
-
Epplen C, Frank G, Gomolka M, Albert E, Nurnberg P, Epplen ET. Dinucleotide repeat polymorphism in the human IL1A gene. Hum Mol Genet 1994;3:1710.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1710
-
-
Epplen, C.1
Frank, G.2
Gomolka, M.3
Albert, E.4
Nurnberg, P.5
Epplen, E.T.6
-
35
-
-
0028365909
-
Integrated human genome-wide maps constructed using the CEPH reference panel
-
Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddena T, Duyk GM, Sheffield VC, et al. Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet 1994;6:388-93.
-
(1994)
Nat Genet
, vol.6
, pp. 388-393
-
-
Buetow, K.H.1
Weber, J.L.2
Ludwigsen, S.3
Scherpbier-Heddena, T.4
Duyk, G.M.5
Sheffield, V.C.6
-
36
-
-
0028231090
-
The 1993-1994 Genethon human genetic linkage map
-
Gyapay G, Morisette VA. The 1993-1994 Genethon human genetic linkage map. Nat Genet 1994;7:246-339.
-
(1994)
Nat Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morisette, V.A.2
-
37
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996;380:152-4.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
-
38
-
-
0008890537
-
Transfer of DNA from agarose gels to nitrocellulose paper
-
Cold Spring Harbor (NY): Cold Spring Harbor Laboratory
-
Maniatis T, Fritsch EF, Sambrook J. Transfer of DNA from agarose gels to nitrocellulose paper. In: Molecular cloning, a laboratory manual. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory; 1982. p. 383.
-
(1982)
Molecular Cloning, a Laboratory Manual
, pp. 383
-
-
Maniatis, T.1
Fritsch, E.F.2
Sambrook, J.3
-
39
-
-
0028913523
-
An E-M algorithm and testing strategy for multiple-locus haplotypes
-
Long JC, Williams RC, Urbanek M. An E-M algorithm and testing strategy for multiple-locus haplotypes. Am J Hum Genet 1995;56: 799-810.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 799-810
-
-
Long, J.C.1
Williams, R.C.2
Urbanek, M.3
-
40
-
-
0030131165
-
Testing for linkage disequilibrium in genotypic data using the expectation-maximization algorithm
-
Slatkin M, Excoffier L. Testing for linkage disequilibrium in genotypic data using the expectation-maximization algorithm. Heredity 1996;76:377-83.
-
(1996)
Heredity
, vol.76
, pp. 377-383
-
-
Slatkin, M.1
Excoffier, L.2
-
41
-
-
0027393037
-
Intraclass and interclass correlations of allele sizes within and between loci in DNA typing data
-
Chakraborty R, Srinivasan MR, de Andrade M. Intraclass and interclass correlations of allele sizes within and between loci in DNA typing data. Genet Soc Am 1993;133:411-9.
-
(1993)
Genet Soc Am
, vol.133
, pp. 411-419
-
-
Chakraborty, R.1
Srinivasan, M.R.2
De Andrade, M.3
-
42
-
-
0029988255
-
A metric map of humans: 23,500 loci in 850 bands
-
Collins A, Frezal J, Teague J, Morton NE. A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci U S A 1996;93:14771-5.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 14771-14775
-
-
Collins, A.1
Frezal, J.2
Teague, J.3
Morton, N.E.4
-
45
-
-
0029941445
-
A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation
-
Siracusa LD, McGrath R, Ma Q, Moskow JJ, Mane J, Christner PJ, et al. A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation. Genome Res 1996;6:300-13.
-
(1996)
Genome Res
, vol.6
, pp. 300-313
-
-
Siracusa, L.D.1
McGrath, R.2
Ma, Q.3
Moskow, J.J.4
Mane, J.5
Christner, P.J.6
-
46
-
-
0023002893
-
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils
-
Sakai LY, Keene DR, Engvall E. Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol 1986;103:2499-509.
-
(1986)
J Cell Biol
, vol.103
, pp. 2499-2509
-
-
Sakai, L.Y.1
Keene, D.R.2
Engvall, E.3
-
47
-
-
3543147330
-
The collagen in scleroderma
-
Fleischmajer R. The collagen in scleroderma. Arch Dermatol 1964;89:437-41.
-
(1964)
Arch Dermatol
, vol.89
, pp. 437-441
-
-
Fleischmajer, R.1
-
48
-
-
3543075921
-
A contribution to the pathogenesis of the changes in the collagen-ground substance equilibrium in morphoea (scleroderma)
-
Musso LA. A contribution to the pathogenesis of the changes in the collagen-ground substance equilibrium in morphoea (scleroderma). Br J Dermatol 1954;66:377-87.
-
(1954)
Br J Dermatol
, vol.66
, pp. 377-387
-
-
Musso, L.A.1
-
49
-
-
3543134383
-
Sclerodermia dermatomyositis (with electronmicrographs)
-
Seville RH. Sclerodermia dermatomyositis (with electronmicrographs). Br J Dermatol 1952;64:467-70.
-
(1952)
Br J Dermatol
, vol.64
, pp. 467-470
-
-
Seville, R.H.1
-
50
-
-
0028582165
-
Identification and characterization of LTBP-2, a novel latent transforming growth factor-beta-binding protein
-
Moren A, Olofsson A, Stenman G, Sahlin P, Kanzaki T, Claesson-Welsh L, et al. Identification and characterization of LTBP-2, a novel latent transforming growth factor-beta-binding protein. J Biol Chem 1994;269:32469-78.
-
(1994)
J Biol Chem
, vol.269
, pp. 32469-32478
-
-
Moren, A.1
Olofsson, A.2
Stenman, G.3
Sahlin, P.4
Kanzaki, T.5
Claesson-Welsh, L.6
-
51
-
-
0028900639
-
Isolation of a novel latent transforming growth factor-beta binding protein (LTBP-3)
-
Yin W, Smiley E, Germiller J, Mecham RP, Florer JB, Wenstrup RJ, et al. Isolation of a novel latent transforming growth factor-beta binding protein (LTBP-3). J Biol Chem 1995;270:10147-60.
-
(1995)
J Biol Chem
, vol.270
, pp. 10147-10160
-
-
Yin, W.1
Smiley, E.2
Germiller, J.3
Mecham, R.P.4
Florer, J.B.5
Wenstrup, R.J.6
-
52
-
-
0027976521
-
Latent transforming growth factor-beta 1 associates to fibroblast extracellular matrix via latent TGF-beta binding protein
-
Taipale J, Miyazono K, Helkin CH, Keski-Oja J. Latent transforming growth factor-beta 1 associates to fibroblast extracellular matrix via latent TGF-beta binding protein. J Cell Biol 1994;124: 171-81.
-
(1994)
J Cell Biol
, vol.124
, pp. 171-181
-
-
Taipale, J.1
Miyazono, K.2
Helkin, C.H.3
Keski-Oja, J.4
-
53
-
-
0023183348
-
Transforming growth factor-beta: Selective increase in glycosaminoglycan synthesis by cultures of fibroblasts from patients with progressive systemic sclerosis
-
Falanga V, Teigs SL, Alstadt SP, Roberts SB, Sporn MB. Transforming growth factor-beta: selective increase in glycosaminoglycan synthesis by cultures of fibroblasts from patients with progressive systemic sclerosis. J Invest Dermatol 1987;89:100-4.
-
(1987)
J Invest Dermatol
, vol.89
, pp. 100-104
-
-
Falanga, V.1
Teigs, S.L.2
Alstadt, S.P.3
Roberts, S.B.4
Sporn, M.B.5
-
55
-
-
0028831359
-
Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype
-
Eldadah ZA, Brenn T, Furthmayr H, Dietz H. Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype. J Clin Invest 1995;95:874-80.
-
(1995)
J Clin Invest
, vol.95
, pp. 874-880
-
-
Eldadah, Z.A.1
Brenn, T.2
Furthmayr, H.3
Dietz, H.4
-
56
-
-
0029665565
-
Fibrillin mutations in Marfan syndrome and related phenotypes
-
Ramirez F. Fibrillin mutations in Marfan syndrome and related phenotypes. Curr Opin Genet Dev 1996;6:309-15.
-
(1996)
Curr Opin Genet Dev
, vol.6
, pp. 309-315
-
-
Ramirez, F.1
-
57
-
-
0027955749
-
Severe neonatal Marfan syndrome resulting from a de novo 3 bp insertion into the fibrillin gene on chromosome 15
-
Milewicz DM, Duvic M. Severe neonatal Marfan syndrome resulting from a de novo 3 bp insertion into the fibrillin gene on chromosome 15. Am J Hum Genet 1994;54:446-53.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 446-453
-
-
Milewicz, D.M.1
Duvic, M.2
-
58
-
-
0029962419
-
Delineation of the Marfan phenotype associated with mutations in exons 23 through 32 of the FBN1 gene
-
Putnam EA, Cho M, Zinn AB, Towbin JA, Byers PH, Milewicz DM. Delineation of the Marfan phenotype associated with mutations in exons 23 through 32 of the FBN1 gene. Am J Med Genet 1996;62:233-42.
-
(1996)
Am J Med Genet
, vol.62
, pp. 233-242
-
-
Putnam, E.A.1
Cho, M.2
Zinn, A.B.3
Towbin, J.A.4
Byers, P.H.5
Milewicz, D.M.6
-
59
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander ES, Schork NJ. Genetic dissection of complex traits. Science 1994;265:2037-48.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
|