-
1
-
-
0019826378
-
Estimation of genetic variation at the DNA level from restriction endonuclease data
-
Ewens, W. J., Spielman R.S. & Harris, H. Estimation of genetic variation at the DNA level from restriction endonuclease data. Proc. Natl., Acad. Sci. USA 6, 3748-3750 (1981).
-
(1981)
Proc. Natl., Acad. Sci. USA
, vol.6
, pp. 3748-3750
-
-
Ewens, W.J.1
Spielman, R.S.2
Harris, H.3
-
2
-
-
0021943341
-
An estimate of unique DNA sequence heterozygosity in the human genome
-
Cooper, D. N., Smith, B.A., Cooke, H.J., Niemann, S. & Schmidte, J. An estimate of unique DNA sequence heterozygosity in the human genome. Hum. Genet. 69, 201-205 (1985).
-
(1985)
Hum. Genet.
, vol.69
, pp. 201-205
-
-
Cooper, D.N.1
Smith, B.A.2
Cooke, H.J.3
Niemann, S.4
Schmidte, J.5
-
3
-
-
0027194903
-
Genomic mismatch scanning : A new approach to genetic linkage mapping
-
Nelson, S.F. et al. Genomic mismatch scanning : a new approach to genetic linkage mapping. Nature Genet. 4, 11-18 (1993).
-
(1993)
Nature Genet.
, vol.4
, pp. 11-18
-
-
Nelson, S.F.1
-
4
-
-
0030751457
-
Identification of the human chromosomal region contain the iridogoniodysgenesis anomaly locus by genomic mismatch scanning
-
Mirzayans, F., Mear, A.J., Guo, S.-W., Pearce W.G. & Walter, M.A. Identification of the human chromosomal region contain the iridogoniodysgenesis anomaly locus by genomic mismatch scanning. Am. J. Hum. Genet. 61, 111-119 (1997).
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 111-119
-
-
Mirzayans, F.1
Mear, A.J.2
Guo, S.-W.3
Pearce, W.G.4
Walter, M.A.5
-
5
-
-
0031913116
-
Genomic mismatch scanning identifies human genomic DNA shared identical by descent
-
Cheung, V. G. & Nelson, S.F. Genomic mismatch scanning identifies human genomic DNA shared identical by descent. Genomics 47, 1-7 (1998).
-
(1998)
Genomics
, vol.47
, pp. 1-7
-
-
Cheung, V.G.1
Nelson, S.F.2
-
6
-
-
0031890925
-
Enrichment for loci identical-by-descent between pairs of mouse or human genomes by genomic mismatch scanning
-
McAllister, L., Penland, L. & Brown, P.O. Enrichment for loci identical-by-descent between pairs of mouse or human genomes by genomic mismatch scanning. Genomics 47, 8-14 (1998).
-
(1998)
Genomics
, vol.47
, pp. 8-14
-
-
McAllister, L.1
Penland, L.2
Brown, P.O.3
-
7
-
-
0029024314
-
Cloning of the β-cell high-affinity sulfonylurea receptor: A regulator of insulin secretion
-
Aguilar-Bryan, L. et al. Cloning of the β-cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science 268, 423-425 (1995).
-
(1995)
Science
, vol.268
, pp. 423-425
-
-
Aguilar-Bryan, L.1
-
8
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas P. M. et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268, 426-428 (1995).
-
(1995)
Science
, vol.268
, pp. 426-428
-
-
Thomas, P.M.1
-
9
-
-
0029658241
-
Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
-
Nestorowicz, A. et al. Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum. Mol. Genet. 5, 1813-1822 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1813-1822
-
-
Nestorowicz, A.1
-
10
-
-
0026637946
-
Initiation of methyl-directed mismatch repair
-
Au, K. G., Welsh, K. & Modrich P. Initiation of methyl-directed mismatch repair. J. Biol. Chem. 267, 12142-12148 (1992).
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 12142-12148
-
-
Au, K.G.1
Welsh, K.2
Modrich, P.3
-
11
-
-
0023056949
-
Genomic analysis II: Isolation of high molecular weight heteroduplex DNA following differential methylase protection and formamide-PERT hybridization
-
Casna, N., Novack, D., Hsu, M. & Ford, D. Genomic analysis II: isolation of high molecular weight heteroduplex DNA following differential methylase protection and formamide-PERT hybridization. Nucleic Acids Res. 14, 7285-7303 (1986).
-
(1986)
Nucleic Acids Res.
, vol.14
, pp. 7285-7303
-
-
Casna, N.1
Novack, D.2
Hsu, M.3
Ford, D.4
-
12
-
-
0023062989
-
DNA mismatch correction
-
Modrich, P. DNA mismatch correction. Ann. Rev. Biochem. 56, 435-466 (1987).
-
(1987)
Ann. Rev. Biochem.
, vol.56
, pp. 435-466
-
-
Modrich, P.1
-
13
-
-
0024287626
-
Mispair specificity of methyl-directed DNA mismatch correction in vitro
-
Su, S. S., Lanhue, R.S., Au, K.G. & Modrich P. Mispair specificity of methyl-directed DNA mismatch correction in vitro. J. Biol. Chem. 263, 6829-6835 (1988).
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 6829-6835
-
-
Su, S.S.1
Lanhue, R.S.2
Au, K.G.3
Modrich, P.4
-
14
-
-
0029913452
-
Mutation detection of MutH, MutL, and MutS mismatch repair proteins
-
Smith, J & Modrich, P. Mutation detection of MutH, MutL, and MutS mismatch repair proteins. Proc. Natl. Acad. Sci. USA 93, 4374-4379 (1996).
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 4374-4379
-
-
Smith, J.1
Modrich, P.2
-
15
-
-
0028894185
-
Linkage disequilibrium as a gene-mapping tool
-
Jorde, L. B. Linkage disequilibrium as a gene-mapping tool. Am. J. Hum. Genet. 56, 11-14 (1995).
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 11-14
-
-
Jorde, L.B.1
-
16
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. & Merikangas, K. The future of genetic studies of complex human diseases. Science 273, 1516-1517 (1996).
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
17
-
-
0029036747
-
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews
-
Glaser, B. et al. Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews. Hum. Mol. Genet. 4, 879-886 (1995).
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 879-886
-
-
Glaser, B.1
-
18
-
-
0027278064
-
A Chromosome 11 YAC library
-
Qin, S. et al. A Chromosome 11 YAC library. Genomics 16, 580-585 (1993).
-
(1993)
Genomics
, vol.16
, pp. 580-585
-
-
Qin, S.1
-
19
-
-
9244250305
-
A high-resolution physical map of human chromosome 11
-
Qin, S. et al. A high-resolution physical map of human chromosome 11. Proc. Natl. Acad. Sci. USA 93, 3149-3154 (1996).
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 3149-3154
-
-
Qin, S.1
-
20
-
-
0017278130
-
Hyperinsulinism in infants and children: Diagnosis and therapy
-
Stanley, C.A. & Baker, L. Hyperinsulinism in infants and children: Diagnosis and therapy. Advances Pediatr. 23, 315-355 (1976).
-
(1976)
Advances Pediatr.
, vol.23
, pp. 315-355
-
-
Stanley, C.A.1
Baker, L.2
-
21
-
-
0028236583
-
Familial hyperinsulinism maps to chromosome 11p14-15.l, 30 cM centromeric to the insulin gene
-
Glaser, B. et al. Familial hyperinsulinism maps to chromosome 11p14-15.l, 30 cM centromeric to the insulin gene. Nature Genet. 7, 185-188 (1994).
-
(1994)
Nature Genet.
, vol.7
, pp. 185-188
-
-
Glaser, B.1
-
22
-
-
0030008587
-
Construction of a YAC contig encompassing the Usher Syndrome Type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1
-
Ayyagari, A. et al. Construction of a YAC contig encompassing the Usher Syndrome Type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1. Genome Res. 6, 504-514 (1996).
-
(1996)
Genome Res.
, vol.6
, pp. 504-514
-
-
Ayyagari, A.1
-
23
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem, B.S. et al. Identification of the cystic fibrosis gene: Genetic analysis. Science 245, 1073-1080 (1989).
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.S.1
-
24
-
-
0028819262
-
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their descent from a small founder population
-
Risch, N. et al. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their descent from a small founder population. Nature Genet. 9, 152-159 (1995).
-
(1995)
Nature Genet.
, vol.9
, pp. 152-159
-
-
Risch, N.1
-
25
-
-
0026949420
-
Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
-
Ha&stbacka, J. et al. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nature Genet. 2, 204-211 (1992).
-
(1992)
Nature Genet.
, vol.2
, pp. 204-211
-
-
Hastbacka, J.1
-
26
-
-
0014219558
-
Fractionation of nucleic acid on benzoylated-naphthoylated DEAE cellulose
-
Sedat, J. W., Kelly, R.B. & Sinsheimer, R.L. Fractionation of nucleic acid on benzoylated-naphthoylated DEAE cellulose. J. Mol. Biol. 26, 537-540 (1967).
-
(1967)
J. Mol. Biol.
, vol.26
, pp. 537-540
-
-
Sedat, J.W.1
Kelly, R.B.2
Sinsheimer, R.L.3
-
27
-
-
0021253525
-
Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing
-
Henikoff, S. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene 28, 351-360 (1984).
-
(1984)
Gene
, vol.28
, pp. 351-360
-
-
Henikoff, S.1
-
28
-
-
0026725180
-
Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification
-
Lengauer, C., Green, E.D. & Cremer, T. Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification. Genomics 13, 826-828 (1992).
-
(1992)
Genomics
, vol.13
, pp. 826-828
-
-
Lengauer, C.1
Green, E.D.2
Cremer, T.3
-
29
-
-
0029812283
-
A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization
-
Shalon, D., Smith, S.J. & Brown, P.O. A DNA microarray system for analyzing complex DNA samples using two-color fluorescent probe hybridization. Genome Res. 6, 639-645 (1996).
-
(1996)
Genome Res.
, vol.6
, pp. 639-645
-
-
Shalon, D.1
Smith, S.J.2
Brown, P.O.3
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