-
1
-
-
84942947953
-
Advances in molecular analysis of fragile X syndrome
-
Warren ST, Nelson DL: Advances in molecular analysis of fragile X syndrome. JAMA 1994; 271: 536-542.
-
(1994)
JAMA
, vol.271
, pp. 536-542
-
-
Warren, S.T.1
Nelson, D.L.2
-
2
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group: A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993; 72: 971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
3
-
-
0030795968
-
The CAG/polyglutamine tract diseases: Gene products and molecular pathogenesis
-
Koshy BT, Zoghbi HY: The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis. Brain Pathol 1997; 7: 927-942.
-
(1997)
Brain Pathol
, vol.7
, pp. 927-942
-
-
Koshy, B.T.1
Zoghbi, H.Y.2
-
4
-
-
0025800526
-
Androgen receptor gene mutation in linked spinal and bulbar muscular atrophy
-
LaSpada AR et al: Androgen receptor gene mutation in linked spinal and bulbar muscular atrophy. Nature 1992; 352: 77-79.
-
(1992)
Nature
, vol.352
, pp. 77-79
-
-
LaSpada, A.R.1
-
5
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide R et al: Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet 1994; 6: 14-18.
-
(1994)
Nature Genet
, vol.6
, pp. 14-18
-
-
Koide, R.1
-
6
-
-
0026601924
-
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
-
Harley HG et al: Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature 1992; 355: 545-546.
-
(1992)
Nature
, vol.355
, pp. 545-546
-
-
Harley, H.G.1
-
7
-
-
0026584805
-
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
-
Buxton J et al: Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 1992; 355: 547-548.
-
(1992)
Nature
, vol.355
, pp. 547-548
-
-
Buxton, J.1
-
8
-
-
84970050019
-
Human genes containing polymorphic trinucleotide repeats
-
Riggins GJ et al: Human genes containing polymorphic trinucleotide repeats. Nature Genet 1992; 2: 186-191.
-
(1992)
Nature Genet
, vol.2
, pp. 186-191
-
-
Riggins, G.J.1
-
9
-
-
0027297703
-
Novel triplet repeat containing genes in human brain: Cloning, expression and length polymorphisms
-
Li S-H et al: Novel triplet repeat containing genes in human brain: cloning, expression and length polymorphisms. Genomics 1993; 16: 572-579.
-
(1993)
Genomics
, vol.16
, pp. 572-579
-
-
Li, S.-H.1
-
10
-
-
8944262197
-
Survey of CAG/CTG repeats in human cDNAs representing new genes: Candidates for inherited neurological disorders
-
Neri C et al: Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders. Hum Mol Genet 1996; 5(7): 1001-1009.
-
(1996)
Hum Mol Genet
, vol.5
, Issue.7
, pp. 1001-1009
-
-
Neri, C.1
-
11
-
-
0028827297
-
Characterization of four novel CAG repeat-containing cDNAs
-
Jiang JX, Deprez RH, Zwarthoff EC, Riegman PH: Characterization of four novel CAG repeat-containing cDNAs. Genomics 1995; 30(1): 91-93.
-
(1995)
Genomics
, vol.30
, Issue.1
, pp. 91-93
-
-
Jiang, J.X.1
Deprez, R.H.2
Zwarthoff, E.C.3
Riegman, P.H.4
-
12
-
-
0023066864
-
Selection of clones from libraries: Overview
-
Berger S, Kimmel AR (eds). Academic Press: New York
-
Kimmel AR: Selection of clones from libraries: overview. In: Berger S, Kimmel AR (eds). Methods in Enzymology. Academic Press: New York, 1987, vol 152, pp 393-398.
-
(1987)
Methods in Enzymology
, vol.152
, pp. 393-398
-
-
Kimmel, A.R.1
-
13
-
-
0028907452
-
Direct sequencing of trinucleotide repeats from cosmid genomic DNA templates
-
Philibert RA et al: Direct sequencing of trinucleotide repeats from cosmid genomic DNA templates. Anal Biochem 1995; 225: 372-374.
-
(1995)
Anal Biochem
, vol.225
, pp. 372-374
-
-
Philibert, R.A.1
-
14
-
-
0023552653
-
Guide to molecular cloning techniques
-
Berger SL, Kimmel AR (eds). Academic Press, New York
-
Wallace RB, Miyada CG: Guide to molecular cloning techniques. In Berger SL, Kimmel AR (eds). Methods in Enzymology. Academic Press, New York, 1987, vol 152, pp 432-442.
-
(1987)
Methods in Enzymology
, vol.152
, pp. 432-442
-
-
Wallace, R.B.1
Miyada, C.G.2
-
15
-
-
0025183708
-
Basic local alignment search tool
-
Altschul SF et al: Basic local alignment search tool. J Mol Biol 1990; 215: 403-410.
-
(1990)
J Mol Biol
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
-
16
-
-
0026351408
-
Locating protein-coding regions in Auman DNA sequences by a multiple sensorneural network approach
-
Uberbacher EC, Mural RJ: Locating protein-coding regions in Auman DNA sequences by a multiple sensorneural network approach. Proc Nat Acad Sci USA 1991; 88: 11261-11265.
-
(1991)
Proc Nat Acad Sci USA
, vol.88
, pp. 11261-11265
-
-
Uberbacher, E.C.1
Mural, R.J.2
-
18
-
-
0026605766
-
A simple method for simultaneous R- or G-banding and fluorescence in situhybridization of small single copy genes
-
Lemieux N, Dutrillaux B, Viegas-Pequignot E: A simple method for simultaneous R- or G-banding and fluorescence in situhybridization of small single copy genes. Cytogenetics Cell Genet 1992; 59: 311-312.
-
(1992)
Cytogenetics Cell Genet
, vol.59
, pp. 311-312
-
-
Lemieux, N.1
Dutrillaux, B.2
Viegas-Pequignot, E.3
-
19
-
-
0028886713
-
Molecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase gene
-
Tenhunen K et al: Molecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase gene. Genomics 1995; 30: 244-250.
-
(1995)
Genomics
, vol.30
, pp. 244-250
-
-
Tenhunen, K.1
-
20
-
-
0007358460
-
Rapid detection of human chromosome 21 aberrations by in situ hybridization
-
Lichter P et al: Rapid detection of human chromosome 21 aberrations by in situ hybridization. Proc Natl Acad Sci USA 1988; 85: 9664-9668.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 9664-9668
-
-
Lichter, P.1
-
21
-
-
0343319476
-
Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4
-
Pinkel D et al: Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. . Proc Natl Acad Sci USA 1988; 85: 9138-9142.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 9138-9142
-
-
Pinkel, D.1
-
22
-
-
0028959961
-
The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22
-
Rytkonen EM et al: The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22. Cell Genet 1995; 68: 61-63.
-
(1995)
Cell Genet
, vol.68
, pp. 61-63
-
-
Rytkonen, E.M.1
-
23
-
-
0028823968
-
Visual mapping by fiber-FISH
-
Heiskanen M et al: Visual mapping by fiber-FISH. Genomics 1995; 30: 31-36.
-
(1995)
Genomics
, vol.30
, pp. 31-36
-
-
Heiskanen, M.1
-
25
-
-
0028885533
-
Survey of trinucleotide repeats in the human genome: Assessment of their utility as genetic markers
-
Gastier JM et al: Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. Hum Mol Genet 1995; 4: 1829-1836.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1829-1836
-
-
Gastier, J.M.1
-
26
-
-
0029912537
-
n dynamic mutations
-
n dynamic mutations. Genomics 1996; 32: 75-85.
-
(1996)
Genomics
, vol.32
, pp. 75-85
-
-
Gastier, J.M.1
-
27
-
-
17744404331
-
Chromosomal assignment of 2900 triand tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2
-
Sunden SLF et al: Chromosomal assignment of 2900 triand tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics 1996; 32: 15-20.
-
(1996)
Genomics
, vol.32
, pp. 15-20
-
-
Sunden, S.L.F.1
-
28
-
-
0028197078
-
Frequency and stability of the fragile X mutation
-
Reiss AJ et al: Frequency and stability of the fragile X mutation. Hum Mol Genet 1994; 3: 393-398.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 393-398
-
-
Reiss, A.J.1
-
29
-
-
0028176566
-
Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequence: Implication for human genetic diseases
-
Stallings RL: Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequence: implication for human genetic diseases. Genomics 1994; 21: 116-121.
-
(1994)
Genomics
, vol.21
, pp. 116-121
-
-
Stallings, R.L.1
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