-
1
-
-
0026347628
-
Fragile X genotype characterized by an unstable region of DNA
-
Yu, S. et al. Fragile X genotype characterized by an unstable region of DNA Science 252, 1179-1181 (1991)
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
-
2
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CCG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A J.M H. et al. Identification of a gene (FMR-1) containing a CCG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65, 905-914 (1991)
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
-
3
-
-
0025800165
-
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
-
Kremer, E.J. et al. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science 252, 1711-1714 (1991)
-
(1991)
Science
, vol.252
, pp. 1711-1714
-
-
Kremer, E.J.1
-
4
-
-
0026345716
-
Variation of the CCG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Fu, Y.H. et al. Variation of the CCG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 67, 1047-1058 (1991).
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
-
5
-
-
0027203684
-
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
-
Knight, S.J. et al. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell 74, 127-134, (1993).
-
(1993)
Cell
, vol.74
, pp. 127-134
-
-
Knight, S.J.1
-
6
-
-
0028099702
-
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
-
Parrish, J.E. et al. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nature Genet. 8, 229-235 (1994).
-
(1994)
Nature Genet.
, vol.8
, pp. 229-235
-
-
Parrish, J.E.1
-
7
-
-
0027981933
-
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
-
Nancarrow, J.K. et al Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science 264, 1938-1941 (1994).
-
(1994)
Science
, vol.264
, pp. 1938-1941
-
-
Nancarrow, J.K.1
-
8
-
-
0028896099
-
Association of a chromosome deletion syndrome with fragile site within the proto-oncogene CBL2
-
Jones, C., et al Association of a chromosome deletion syndrome with fragile site within the proto-oncogene CBL2 Nature 376, 145-149(1995).
-
(1995)
Nature
, vol.376
, pp. 145-149
-
-
Jones, C.1
-
9
-
-
0026865445
-
Characterization of a new rare fragile site easily confused with the fragile X
-
Sutherland G.R. & Baker, E. Characterization of a new rare fragile site easily confused with the fragile X. Hum. Mol. Genet 1, 111-113 (1992).
-
(1992)
Hum. Mol. Genet
, vol.1
, pp. 111-113
-
-
Sutherland, G.R.1
Baker, E.2
-
10
-
-
0027991895
-
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap
-
Knight, S.J.L. et al. Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap. Am J. Hum. Genet. 55, 81-86 (1994).
-
(1994)
Am J. Hum. Genet.
, vol.55
, pp. 81-86
-
-
Knight, S.J.L.1
-
11
-
-
0027968066
-
Segregation of FRAXE in a large family: Clinical, psychometric, cytogenetic, and molecular data
-
Hamel, B C.J. et al. Segregation of FRAXE in a large family: Clinical, psychometric, cytogenetic, and molecular data. Am J Hum Genet. 55, 923-931 (1994)
-
(1994)
Am J Hum Genet.
, vol.55
, pp. 923-931
-
-
Hamel, B.C.J.1
-
12
-
-
0028933941
-
FRAXE and mental retardation
-
Mulley, J C. et al. FRAXE and mental retardation J Med. Genet.32, 162-169 (1995).
-
(1995)
J Med. Genet.
, vol.32
, pp. 162-169
-
-
Mulley, J.C.1
-
13
-
-
0028937577
-
Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: Identification of a gene near FRAXE
-
Gedeon, A.K. et al. Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: Identification of a gene near FRAXE. Am. J. Hum Genet. 56, 907-914 (1995).
-
(1995)
Am. J. Hum Genet.
, vol.56
, pp. 907-914
-
-
Gedeon, A.K.1
-
14
-
-
3643109607
-
Identification of a FRAXE microdeletion associated with a complex mosaic FRAXA mutation
-
Brown, T et al. Identification of a FRAXE microdeletion associated with a complex mosaic FRAXA mutation 6th X Chromosome Workshop, S13 (1995).
-
(1995)
6th X Chromosome Workshop
, vol.S13
-
-
Brown, T.1
-
15
-
-
84970050019
-
Human genes containing polymorphic trinucleotide repeats
-
Riggins. G.J. et al. Human genes containing polymorphic trinucleotide repeats. Nature Genet. 2, 186-191 (1992).
-
(1992)
Nature Genet.
, vol.2
, pp. 186-191
-
-
Riggins, G.J.1
-
16
-
-
0025819499
-
The sequence of the human and mouse c-cbl proto-oncogenes shows proline -rich domain and leucine zipper-like motif
-
Blake, T.J., Shapiro, M Morse, H.C. & Langdon, W.Y The sequence of the human and mouse c-cbl proto-oncogenes shows proline -rich domain and leucine zipper-like motif. Oncogens 6, 653-657 (1991)
-
(1991)
Oncogens
, vol.6
, pp. 653-657
-
-
Blake, T.J.1
Shapiro, M.2
Morse, H.C.3
Langdon, W.Y.4
-
17
-
-
0022552131
-
Point mutation define a sequence flanking the AUG initiation codon that modulates translation by eucaryotic ribosomes
-
Kozak, M. Point mutation define a sequence flanking the AUG initiation codon that modulates translation by eucaryotic ribosomes. Cell 44, 283-292 (1986).
-
(1986)
Cell
, vol.44
, pp. 283-292
-
-
Kozak, M.1
-
18
-
-
0025183708
-
Basic local alignment tool
-
Altchul, D et al. Basic local alignment tool. J Mol Biol. 215, 403-410 (1990)
-
(1990)
J Mol Biol.
, vol.215
, pp. 403-410
-
-
Altchul, D.1
-
19
-
-
0027173436
-
Genes on chromosomes 4, 9 and 19 involved in 11q23 abnormalities in acute leukemias share sequence sequence homology and/or common motifs. Proc
-
Nakamura, T. et al. Genes on chromosomes 4, 9 and 19 involved in 11q23 abnormalities in acute leukemias share sequence sequence homology and/or common motifs. Proc Natl. Acad. Sci. USA 90, 4631-1635 (1993).
-
(1993)
Natl. Acad. Sci. USA
, vol.90
, pp. 4631-11635
-
-
Nakamura, T.1
-
20
-
-
0027462322
-
A serine/proline-rich protein is fused to HRX in t(4;11) acute leukemias
-
Morrissey, J. et al. A serine/proline-rich protein is fused to HRX in t(4;11) acute leukemias. Blood 81, 1124-1131 (1993).
-
(1993)
Blood
, vol.81
, pp. 1124-1131
-
-
Morrissey, J.1
-
21
-
-
0024340524
-
The proline-rich transcription activator of CTF/NF-I is distinct from the replication and DNA binding domain
-
Mermod, N , O'Neil, E A , Kelly, T.J. & Tjian, R. The proline-rich transcription activator of CTF/NF-I is distinct from the replication and DNA binding domain. Cell 58, 741-753 (1989).
-
(1989)
Cell
, vol.58
, pp. 741-753
-
-
Mermod, N.1
O'Neil, E.A.2
Kelly, T.J.3
Tjian, R.4
-
22
-
-
0015336653
-
A theory of X-linkage of major intellectual traits
-
Lehrke, R.G A theory of X-linkage of major intellectual traits. Am J Med Defic 76, 611-619 (1972)
-
(1972)
Am J Med Defic
, vol.76
, pp. 611-619
-
-
Lehrke, R.G.1
-
23
-
-
85087231062
-
How many X-linked genes for non-specific mental retardation (MRX) are there
-
in the press
-
Gedeon, A K., Donnelly, A J., Bronwyn, K , Turner, G. & Mulley, J C How many X-linked genes for non-specific mental retardation (MRX) are there Am. J. Med Genet (in the press).
-
Am. J. Med Genet
-
-
Gedeon, A.K.1
Donnelly, A.J.2
Bronwyn, K.3
Turner, G.4
Mulley, J.C.5
-
24
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski, P & Sacci, N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162, 156-159 (1987).
-
(1987)
Anal. Biochem.
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacci, N.2
-
25
-
-
0023001208
-
Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma
-
Lee, E.Y & Lee, WH. Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma. Proc. Natl. Acad. Sci USA 83, 6337-6341 (1986)
-
(1986)
Proc. Natl. Acad. Sci USA
, vol.83
, pp. 6337-6341
-
-
Lee, E.Y.1
Lee, W.H.2
|