-
1
-
-
85052643252
-
Meadowcraft rockshelter, 1977: An overview
-
Adovasio JM, Gunn JD, Donahue J, Stukenrath R (1978) Meadowcraft rockshelter, 1977: an overview. Am Antiquity 43: 632-651
-
(1978)
Am Antiquity
, vol.43
, pp. 632-651
-
-
Adovasio, J.M.1
Gunn, J.D.2
Donahue, J.3
Stukenrath, R.4
-
2
-
-
0021688283
-
Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines
-
Anderson MA, Gusella J (1984) Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines. In Vitro 20:856-858
-
(1984)
In Vitro
, vol.20
, pp. 856-858
-
-
Anderson, M.A.1
Gusella, J.2
-
3
-
-
0025866192
-
Ethnic distribution of myotonic dystrophy gene
-
Ashizawa T, Epstein HF (1991) Ethnic distribution of myotonic dystrophy gene. Lancet 338:642-643
-
(1991)
Lancet
, vol.338
, pp. 642-643
-
-
Ashizawa, T.1
Epstein, H.F.2
-
4
-
-
0026567370
-
Cloning of the essential myotonic dystrophy region and mapping of the putative defect
-
Aslanidis C, Jansen G, Amemiya C, Shutler G, Mahadevan M, Tsilfidis C, Chen C, et al (1992) Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature 355:548-551
-
(1992)
Nature
, vol.355
, pp. 548-551
-
-
Aslanidis, C.1
Jansen, G.2
Amemiya, C.3
Shutler, G.4
Mahadevan, M.5
Tsilfidis, C.6
Chen, C.7
-
5
-
-
0027256028
-
Intergenerational stability of the myotonic dystrophy protomutation
-
Barceló JM, Mahadevan MS, Tsilfidis C, MacKenzie AE, Korneluk RG (1993) Intergenerational stability of the myotonic dystrophy protomutation. Hum Mol Genet 2:705-709
-
(1993)
Hum Mol Genet
, vol.2
, pp. 705-709
-
-
Barceló, J.M.1
Mahadevan, M.S.2
Tsilfidis, C.3
MacKenzie, A.E.4
Korneluk, R.G.5
-
8
-
-
0026087208
-
Drift, admixture, and selection in human evolution: A study with DNA polymorphisms
-
Bowcock AM, Kidd JR, Mountain JL, Hebert JM, Cartenuto L, Kidd KK, Cavalli-Sforza LL (1991) Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proc Natl Acad Sci USA 88: 839-843
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 839-843
-
-
Bowcock, A.M.1
Kidd, J.R.2
Mountain, J.L.3
Hebert, J.M.4
Cartenuto, L.5
Kidd, K.K.6
Cavalli-Sforza, L.L.7
-
9
-
-
0026566108
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein family member
-
Brook, JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K, et al (1992) Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein family member. Cell 68:799-808
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
Buckler, A.J.4
Church, D.5
Aburatani, H.6
Hunter, K.7
-
10
-
-
0027420436
-
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)
-
Brunner HG, Bruggenwirth HT, Nillesen W, Jansen G, Hamel BCJ, Hoppe RLE, de Die CEM, et al (1993) Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM). Am J Hum Genet 53:1016-1023
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1016-1023
-
-
Brunner, H.G.1
Bruggenwirth, H.T.2
Nillesen, W.3
Jansen, G.4
Hamel, B.C.J.5
Hoppe, R.L.E.6
De Die, C.E.M.7
-
11
-
-
0026584805
-
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
-
Buxton J, Shelbourne P, Davies J, Jones C, Van Tongeren T, Aslanidis C, de Jong P, et al (1992) Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 355:547-548
-
(1992)
Nature
, vol.355
, pp. 547-548
-
-
Buxton, J.1
Shelbourne, P.2
Davies, J.3
Jones, C.4
Van Tongeren, T.5
Aslanidis, C.6
De Jong, P.7
-
12
-
-
0028784297
-
Evolution of haplotypes at the DRD2 locus
-
Castiglione CM, Deinard AS, Speed WC, Sirugo G, Rosenbaum HC, Zhang Y, Grandy DK, et al (1995) Evolution of haplotypes at the DRD2 locus. Am J Hum Genet 57: 1445-1456
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1445-1456
-
-
Castiglione, C.M.1
Deinard, A.S.2
Speed, W.C.3
Sirugo, G.4
Rosenbaum, H.C.5
Zhang, Y.6
Grandy, D.K.7
-
14
-
-
0015806932
-
Dystrophia myotonica in Nigerian family
-
Dada TO (1973) Dystrophia myotonica in Nigerian family. East Afr Med J 50:213-228
-
(1973)
East Afr Med J
, vol.50
, pp. 213-228
-
-
Dada, T.O.1
-
15
-
-
0026450773
-
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations
-
Davies JD, Yamagata H, Shelbourne P, Buxton J, Ogihara T, Nokelainen P, Nakagawa M, et al (1992) Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations. J Med Genet 29:766-769
-
(1992)
J Med Genet
, vol.29
, pp. 766-769
-
-
Davies, J.D.1
Yamagata, H.2
Shelbourne, P.3
Buxton, J.4
Ogihara, T.5
Nokelainen, P.6
Nakagawa, M.7
-
16
-
-
19144370801
-
Distribution and evolution of CTG repeats in the myotonin protein kinase gene in human populations
-
Deka R, Majumder PP, Shriver MD, Stivers DN, Zhong Y, Yu LM, Barrantes R, et al (1996) Distribution and evolution of CTG repeats in the myotonin protein kinase gene in human populations. Genome Res 6:142-154
-
(1996)
Genome Res
, vol.6
, pp. 142-154
-
-
Deka, R.1
Majumder, P.P.2
Shriver, M.D.3
Stivers, D.N.4
Zhong, Y.5
Yu, L.M.6
Barrantes, R.7
-
18
-
-
0028325745
-
Mutational processes of simple-sequence repeat loci in human populations
-
DiRienzo A, Peterson AC, Garza JC, Valdes AM, Slatkin M, Freimer NB (1994) Mutational processes of simple-sequence repeat loci in human populations. Proc Natl Acad Sci USA 91:3166-3170
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3166-3170
-
-
DiRienzo, A.1
Peterson, A.C.2
Garza, J.C.3
Valdes, A.M.4
Slatkin, M.5
Freimer, N.B.6
-
19
-
-
0026598119
-
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
-
Fu YH, Pizzuti A, Fenwick RGJr, King J, Rajnarayan S, Dunne PW, Dubel J, et al (1992) An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science 255: 1256-1258
-
(1992)
Science
, vol.255
, pp. 1256-1258
-
-
Fu, Y.H.1
Pizzuti, A.2
Fenwick Jr., R.G.3
King, J.4
Rajnarayan, S.5
Dunne, P.W.6
Dubel, J.7
-
20
-
-
0029832024
-
Founder effect and the prevalence of myotonic dystrophy in South Africans: Molecular studies
-
Goldman A, Krause A, Ramsay M, Jenkins T (1996a) Founder effect and the prevalence of myotonic dystrophy in South Africans: molecular studies. Am J Hum Genet 59:445-452
-
(1996)
Am J Hum Genet
, vol.59
, pp. 445-452
-
-
Goldman, A.1
Krause, A.2
Ramsay, M.3
Jenkins, T.4
-
21
-
-
0027958086
-
Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats
-
Goldman A, Ramsay M, Jenkins T (1994) Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats. J Med Genet 31:37-40
-
(1994)
J Med Genet
, vol.31
, pp. 37-40
-
-
Goldman, A.1
Ramsay, M.2
Jenkins, T.3
-
22
-
-
0029038408
-
New founder haplotypes at the myotonic dystrophy locus in Southern Africa
-
_ (1995) New founder haplotypes at the myotonic dystrophy locus in Southern Africa. Am J Hum Genet 56: 1373-1378
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1373-1378
-
-
-
23
-
-
0030052440
-
Ethnicity and myotonic dystrophy: A possible explanation for its absence in sub-Saharan Africa
-
_ (1996b) Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa. Ann Hum Genet 60:57-65
-
(1996)
Ann Hum Genet
, vol.60
, pp. 57-65
-
-
-
24
-
-
0026601924
-
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
-
Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS, et al (1992) Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature 355:545-546
-
(1992)
Nature
, vol.355
, pp. 545-546
-
-
Harley, H.G.1
Brook, J.D.2
Rundle, S.A.3
Crow, S.4
Reardon, W.5
Buckler, A.J.6
Harper, P.S.7
-
25
-
-
0027485748
-
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy
-
Harley HG, Rundle SA, MacMillan JC, Myring J, Brook JD, Crow S, Reardon W, et al (1993) Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Am J Hum Genet 52: 1164-1174
-
(1993)
Am J Hum Genet
, vol.52
, pp. 1164-1174
-
-
Harley, H.G.1
Rundle, S.A.2
MacMillan, J.C.3
Myring, J.4
Brook, J.D.5
Crow, S.6
Reardon, W.7
-
27
-
-
0029837246
-
Myotonic dystrophy: Will the real gene please step forward!
-
Harris S, Moncrieff C, Johnson K (1996) Myotonic dystrophy: will the real gene please step forward! Hum Mol Genet 5: 1417-1423
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1417-1423
-
-
Harris, S.1
Moncrieff, C.2
Johnson, K.3
-
28
-
-
0029372419
-
HAPLO: A program using the EM algorithm to estimate the frequencies of multi-site haplotypes
-
Hawley ME, Kidd KK (1995) HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered 86:409-411
-
(1995)
J Hered
, vol.86
, pp. 409-411
-
-
Hawley, M.E.1
Kidd, K.K.2
-
29
-
-
0000710372
-
Late Miocene and early Pliocene hominoids from Africa
-
Corruccini RS, Ciochon RL (eds). Prentice Hall, Englewood Cliffs, NJ
-
Hill A (1994) Late Miocene and early Pliocene hominoids from Africa. In: Corruccini RS, Ciochon RL (eds) Integrative paths to the past: paleoanthropological advances in honor of F. Clarke Howell. Prentice Hall, Englewood Cliffs, NJ, pp 123-145
-
(1994)
Integrative Paths to the Past: Paleoanthropological Advances in Honor of F. Clarke Howell
, pp. 123-145
-
-
Hill, A.1
-
30
-
-
0026457624
-
The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy
-
Hunter A, Tsilfidis C, Mettler G, Jacob P, Mahadevan M, Surh L, Korneluk R, et al (1992) The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy. J Med Genet 29:774-779
-
(1992)
J Med Genet
, vol.29
, pp. 774-779
-
-
Hunter, A.1
Tsilfidis, C.2
Mettler, G.3
Jacob, P.4
Mahadevan, M.5
Surh, L.6
Korneluk, R.7
-
32
-
-
0029038947
-
Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus
-
Jansen G, Bachner D, Coerwinkel M, Wormskamp N, Hameister H, Wieringa B (1995) Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus. Hum Mol Genet 4:843-852
-
(1995)
Hum Mol Genet
, vol.4
, pp. 843-852
-
-
Jansen, G.1
Bachner, D.2
Coerwinkel, M.3
Wormskamp, N.4
Hameister, H.5
Wieringa, B.6
-
33
-
-
8944235350
-
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice
-
Jansen G, Groenen PJ, Bachner D, Jap PH, Coerwinkel M, Oerlemans F, van den Broek W, et al (1996) Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice. Nat Genet 13:316-324
-
(1996)
Nat Genet
, vol.13
, pp. 316-324
-
-
Jansen, G.1
Groenen, P.J.2
Bachner, D.3
Jap, P.H.4
Coerwinkel, M.5
Oerlemans, F.6
Van Den Broek, W.7
-
34
-
-
85030337971
-
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus
-
in press
-
Kidd KK, Morar B, Castiglione CM, Zhao H, Pakstis AJ, Speed WC, Bonne-Tamir B, et al. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Hum Genet (in press)
-
Hum Genet
-
-
Kidd, K.K.1
Morar, B.2
Castiglione, C.M.3
Zhao, H.4
Pakstis, A.J.5
Speed, W.C.6
Bonne-Tamir, B.7
-
35
-
-
0029937381
-
DRD2 haplotypes containing the TaqI A1 allele: Implications for alcoholism research
-
Kidd KK, Pakstis AJ, Castiglione CM, Kidd JR, Speed WC, Goldman D, Knowler WC, et al (1996) DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research. Alcohol Clin Exp Res 20:697-705
-
(1996)
Alcohol Clin Exp Res
, vol.20
, pp. 697-705
-
-
Kidd, K.K.1
Pakstis, A.J.2
Castiglione, C.M.3
Kidd, J.R.4
Speed, W.C.5
Goldman, D.6
Knowler, W.C.7
-
36
-
-
0028143949
-
Neurologic genetic diseases of Jewish people
-
Korczyn AD (1994) Neurologic genetic diseases of Jewish people. Biomed Pharmacother 48:391-397
-
(1994)
Biomed Pharmacother
, vol.48
, pp. 391-397
-
-
Korczyn, A.D.1
-
37
-
-
0029161979
-
Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing
-
Krahe R, Ashizawa T, Abbruzzese C, Roeder E, Carango P, Giacanelli M, Funanage VL, et al (1995a) Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. Genomics 28:1-14
-
(1995)
Genomics
, vol.28
, pp. 1-14
-
-
Krahe, R.1
Ashizawa, T.2
Abbruzzese, C.3
Roeder, E.4
Carango, P.5
Giacanelli, M.6
Funanage, V.L.7
-
38
-
-
0028947051
-
De novo myotonic dystrophy mutation in a Nigerian kindred
-
Krahe R, Eckhart M, Ogunniyi AO, Osuntokun BO, Siciliano MJ, Ashizawa T (1995b) De novo myotonic dystrophy mutation in a Nigerian kindred. Am J Hum Genet 56: 1067-1074
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1067-1074
-
-
Krahe, R.1
Eckhart, M.2
Ogunniyi, A.O.3
Osuntokun, B.O.4
Siciliano, M.J.5
Ashizawa, T.6
-
39
-
-
0002907949
-
The interaction of selection and linkage. I. General considerations: Heterotic models
-
Lewontin RC (1964) The interaction of selection and linkage. I. General considerations: heterotic models. Genetics 49: 49-67
-
(1964)
Genetics
, vol.49
, pp. 49-67
-
-
Lewontin, R.C.1
-
40
-
-
0027314352
-
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene
-
Lichter JB, Barr CL, Kennedy JL, van Tol HHM, Kidd KK, Livak KJ (1993) A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. Hum Mol Genet 2: 767-773
-
(1993)
Hum Mol Genet
, vol.2
, pp. 767-773
-
-
Lichter, J.B.1
Barr, C.L.2
Kennedy, J.L.3
Van Tol, H.H.M.4
Kidd, K.K.5
Livak, K.J.6
-
41
-
-
0022362681
-
Myotonic dystrophy. I. A genealogical study in the northern Transvaal
-
Lotz BP, van den Meyden CH (1985) Myotonic dystrophy. I. A genealogical study in the northern Transvaal. S Afr Med J 67:812-814
-
(1985)
S Afr Med J
, vol.67
, pp. 812-814
-
-
Lotz, B.P.1
Van Den Meyden, C.H.2
-
42
-
-
0027416569
-
Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy
-
Mahadevan MS, Foitzik MA, Surh LC, Korneluk RG (1993) Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy. Genomics 15: 446-448
-
(1993)
Genomics
, vol.15
, pp. 446-448
-
-
Mahadevan, M.S.1
Foitzik, M.A.2
Surh, L.C.3
Korneluk, R.G.4
-
43
-
-
0026603841
-
Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene
-
Mahadevan MS, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, et al (1992) Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene. Science 255:1253-1255
-
(1992)
Science
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.S.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jansen, G.6
Neville, C.7
-
44
-
-
0030741298
-
Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonic gene
-
Mor-Cohen R, Magal N, Gadoth N, Achiron A, Shohat T, Shohat M (1997a) Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonic gene. Am J Med Genet 71:156-159
-
(1997)
Am J Med Genet
, vol.71
, pp. 156-159
-
-
Mor-Cohen, R.1
Magal, N.2
Gadoth, N.3
Achiron, A.4
Shohat, T.5
Shohat, M.6
-
45
-
-
0031105931
-
The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats
-
_ (1997b) The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats. Isr J Med Sci 33:190-193
-
(1997)
Isr J Med Sci
, vol.33
, pp. 190-193
-
-
-
46
-
-
0027532222
-
Explanation for exclusive maternal origin for congenital form of myotonic dystrophy
-
Mulley JC, Staples A, Donnelly A, Gedeon AK, Hecht BK, Nicholson GA, Haan EA, et al (1993) Explanation for exclusive maternal origin for congenital form of myotonic dystrophy. Lancet 341:236-237
-
(1993)
Lancet
, vol.341
, pp. 236-237
-
-
Mulley, J.C.1
Staples, A.2
Donnelly, A.3
Gedeon, A.K.4
Hecht, B.K.5
Nicholson, G.A.6
Haan, E.A.7
-
47
-
-
0028156915
-
High resolution genetic analysis suggests one predisposing haplotype for the origin of the myotonic dystrophy mutation
-
Neville CE, Mahadevan MS, Barcelo JM, Korneluk RG (1994) High resolution genetic analysis suggests one predisposing haplotype for the origin of the myotonic dystrophy mutation. Hum Mol Genet 3:45-51
-
(1994)
Hum Mol Genet
, vol.3
, pp. 45-51
-
-
Neville, C.E.1
Mahadevan, M.S.2
Barcelo, J.M.3
Korneluk, R.G.4
-
49
-
-
0028072993
-
Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations
-
Rubinsztein DC, Leggo J, Amos W, Barton DE, Ferguson-Smith MA (1994) Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations. Hum Mol Genet 3:2031-2035
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2031-2035
-
-
Rubinsztein, D.C.1
Leggo, J.2
Amos, W.3
Barton, D.E.4
Ferguson-Smith, M.A.5
-
50
-
-
0027229993
-
VNTR allele frequency distributions under the stepwise mutation model: A computer simulation approach
-
Shriver MD, Jin L, Chakraborty R, Boerwinkle E (1993) VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. Genetics 134:983-993
-
(1993)
Genetics
, vol.134
, pp. 983-993
-
-
Shriver, M.D.1
Jin, L.2
Chakraborty, R.3
Boerwinkle, E.4
-
51
-
-
0023818575
-
Genetic and fossil evidence for the origin of modern humans
-
Stringer CB, Andrews P (1988) Genetic and fossil evidence for the origin of modern humans. Science 239:1263-1268
-
(1988)
Science
, vol.239
, pp. 1263-1268
-
-
Stringer, C.B.1
Andrews, P.2
-
52
-
-
0029667388
-
Global patterns of linkage disequilibrium at the CD4 locus and modern human origins
-
Tishkoff SA, Dietzsch E, Speed W, Pakstis AJ, Kidd JR, Cheung K-H, Bonne-Tamir B, et al (1996a) Global patterns of linkage disequilibrium at the CD4 locus and modern human origins. Science 271:1380-1387
-
(1996)
Science
, vol.271
, pp. 1380-1387
-
-
Tishkoff, S.A.1
Dietzsch, E.2
Speed, W.3
Pakstis, A.J.4
Kidd, J.R.5
Cheung, K.-H.6
Bonne-Tamir, B.7
-
53
-
-
0029944733
-
Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans
-
Tishkoff SA, Ruano R, Kidd JR, Kidd KK (1996b) Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans. Hum Genet 97:759-764
-
(1996)
Hum Genet
, vol.97
, pp. 759-764
-
-
Tishkoff, S.A.1
Ruano, R.2
Kidd, J.R.3
Kidd, K.K.4
-
54
-
-
0026879229
-
Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
-
Tsilfidis C, MacKenzie AE, Mettler G, Barcelo J, Korneluk RG (1992) Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy. Nat Genet 1:192-195
-
(1992)
Nat Genet
, vol.1
, pp. 192-195
-
-
Tsilfidis, C.1
MacKenzie, A.E.2
Mettler, G.3
Barcelo, J.4
Korneluk, R.G.5
-
55
-
-
0027474097
-
Allele frequencies at microsatellite loci: The stepwise mutation model revisited
-
Valdes AM, Slatkin NB, Freimer NB (1993) Allele frequencies at microsatellite loci: the stepwise mutation model revisited. Genetics 133:737-749
-
(1993)
Genetics
, vol.133
, pp. 737-749
-
-
Valdes, A.M.1
Slatkin, N.B.2
Freimer, N.B.3
-
56
-
-
0028932050
-
Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements
-
Wang YH, Griffith J (1995) Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements. Genomics 25: 570-573
-
(1995)
Genomics
, vol.25
, pp. 570-573
-
-
Wang, Y.H.1
Griffith, J.2
-
57
-
-
0027161022
-
Mutation of human short tandem repeats
-
Weber JL, Wong C (1993) Mutation of human short tandem repeats. Hum Mol Genet 2:1123-1128
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1123-1128
-
-
Weber, J.L.1
Wong, C.2
-
59
-
-
0014552244
-
A molecular time scale for human evolution
-
Wilson AC, Sarich VM (1969) A molecular time scale for human evolution. Proc Natl Acad Sci USA 63:1088-1093
-
(1969)
Proc Natl Acad Sci USA
, vol.63
, pp. 1088-1093
-
-
Wilson, A.C.1
Sarich, V.M.2
-
60
-
-
0030047887
-
Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation
-
Yamagata H, Miki T, Nakagawa M, Johnson K, Deka R, Ogihara T (1996) Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation. Hum Genet 97:145-147
-
(1996)
Hum Genet
, vol.97
, pp. 145-147
-
-
Yamagata, H.1
Miki, T.2
Nakagawa, M.3
Johnson, K.4
Deka, R.5
Ogihara, T.6
-
61
-
-
0026548473
-
Expansion of unstable DNA region in Japanese myotonic dystrophy patients
-
Yamagata H, Miki T, Ogihara T, Nakagawa M, Higuchi I, Osame M, Shelbourne P, et al (1992) Expansion of unstable DNA region in Japanese myotonic dystrophy patients. Lancet 339:692
-
(1992)
Lancet
, vol.339
, pp. 692
-
-
Yamagata, H.1
Miki, T.2
Ogihara, T.3
Nakagawa, M.4
Higuchi, I.5
Osame, M.6
Shelbourne, P.7
-
62
-
-
0028794822
-
Normal variation at the myotonic dystrophy locus in global human populations
-
Zerylnick C, Torroni A, Sherman SL, Warren ST (1995) Normal variation at the myotonic dystrophy locus in global human populations. Am J Hum Genet 56:123-130
-
(1995)
Am J Hum Genet
, vol.56
, pp. 123-130
-
-
Zerylnick, C.1
Torroni, A.2
Sherman, S.L.3
Warren, S.T.4
-
63
-
-
0027982427
-
Studying human mutations by sperm typing: Instability of CAG trinucleotide repeats in the human androgen receptor gene
-
Zhang L, Leeflang EP, Yu J, Arnheim N (1994) Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene. Nat Genet 7:531-535
-
(1994)
Nat Genet
, vol.7
, pp. 531-535
-
-
Zhang, L.1
Leeflang, E.P.2
Yu, J.3
Arnheim, N.4
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