-
1
-
-
0034307480
-
A plea to search for deletion polymorphism through genome scans in populations
-
M. Siniscalco A plea to search for deletion polymorphism through genome scans in populations Trends Genet. 16 2000 435 437
-
(2000)
Trends Genet.
, vol.16
, pp. 435-437
-
-
Siniscalco, M.1
-
2
-
-
17344370150
-
Duplication of 8p23.1: A cytogenetic anomaly with no established clinical significance
-
J.C. Barber Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance J. Med. Genet. 35 1998 491 496
-
(1998)
J. Med. Genet.
, vol.35
, pp. 491-496
-
-
Barber, J.C.1
-
3
-
-
0023795143
-
Polymorphism of MHC class III genes: Definition of restriction fragment linkage groups and evidence for frequent deletions and duplications
-
N. Ghanem Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications Hum. Genet. 79 1988 209 218
-
(1988)
Hum. Genet.
, vol.79
, pp. 209-218
-
-
Ghanem, N.1
-
4
-
-
0025718875
-
Interpretation of polymorphic DNA patterns in the human alpha-amylase multigene family
-
P.C. Groot Interpretation of polymorphic DNA patterns in the human alpha-amylase multigene family Genomics 10 1991 779 785
-
(1991)
Genomics
, vol.10
, pp. 779-785
-
-
Groot, P.C.1
-
5
-
-
0034089182
-
Duplication of chromosome region 8p23.1→p23.3: A benign variant?
-
J.J. Engelen Duplication of chromosome region 8p23.1→p23.3: a benign variant? Am. J. Med. Genet. 91 2000 18 21
-
(2000)
Am. J. Med. Genet.
, vol.91
, pp. 18-21
-
-
Engelen, J.J.1
-
6
-
-
0034331289
-
A frequent deletion polymorphism on chromosome 22q13 identified by representational difference analysis of ovarian cancer
-
H. Lin A frequent deletion polymorphism on chromosome 22q13 identified by representational difference analysis of ovarian cancer Genomics 69 2000 391 394
-
(2000)
Genomics
, vol.69
, pp. 391-394
-
-
Lin, H.1
-
7
-
-
0041386350
-
Polymorphically duplicated genes: Their relevance to phenotypic variation in humans
-
P.R. Buckland Polymorphically duplicated genes: their relevance to phenotypic variation in humans Ann. Med. 35 2003 308 315
-
(2003)
Ann. Med.
, vol.35
, pp. 308-315
-
-
Buckland, P.R.1
-
8
-
-
2342563834
-
Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failure
-
M. Cicoira Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failure Am. J. Med. 116 2004 657 661
-
(2004)
Am. J. Med.
, vol.116
, pp. 657-661
-
-
Cicoira, M.1
-
9
-
-
0035864815
-
Frequent germline deletion polymorphism of chromosomal region 8p12-p21 identified as a recurrent homozygous deletion in human tumors
-
B. Ryu Frequent germline deletion polymorphism of chromosomal region 8p12-p21 identified as a recurrent homozygous deletion in human tumors Genomics 72 2001 108 112
-
(2001)
Genomics
, vol.72
, pp. 108-112
-
-
Ryu, B.1
-
10
-
-
0032837669
-
Genetics of HIV-1 infection: Chemokine receptor CCR5 polymorphism and its consequences
-
M. Carrington Genetics of HIV-1 infection: chemokine receptor CCR5 polymorphism and its consequences Hum. Mol. Genet. 8 1999 1939 1945
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1939-1945
-
-
Carrington, M.1
-
11
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
S. Solinas-Toldo Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances Genes Chromosomes Cancer 20 1997 399 407
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
-
12
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
D. Pinkel High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays Nat. Genet. 20 1998 207 211
-
(1998)
Nat. Genet.
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
-
13
-
-
0141994858
-
Genomic microarrays in human genetic disease and cancer
-
D.G. Albertson, and D. Pinkel Genomic microarrays in human genetic disease and cancer Hum. Mol. Genet. 12 2003 R145 R152
-
(2003)
Hum. Mol. Genet.
, vol.12
-
-
Albertson, D.G.1
Pinkel, D.2
-
14
-
-
1642473037
-
Genomic microarrays in the spotlight
-
K.K. Mantripragada Genomic microarrays in the spotlight Trends Genet. 20 2004 87 94
-
(2004)
Trends Genet.
, vol.20
, pp. 87-94
-
-
Mantripragada, K.K.1
-
15
-
-
0035252636
-
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
-
C.E. Bruder High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH Hum. Mol. Genet. 10 2001 271 282
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 271-282
-
-
Bruder, C.E.1
-
16
-
-
0036173663
-
Array-based comparative genomic hybridization for the differential diagnosis of renal cell cancer
-
M. Wilhelm Array-based comparative genomic hybridization for the differential diagnosis of renal cell cancer Cancer Res. 62 2002 957 960
-
(2002)
Cancer Res.
, vol.62
, pp. 957-960
-
-
Wilhelm, M.1
-
17
-
-
0036830160
-
Amplicon mapping and transcriptional analysis pinpoint cyclin L as a candidate oncogene in head and neck cancer
-
R. Redon Amplicon mapping and transcriptional analysis pinpoint cyclin L as a candidate oncogene in head and neck cancer Cancer Res. 62 2002 6211 6217
-
(2002)
Cancer Res.
, vol.62
, pp. 6211-6217
-
-
Redon, R.1
-
18
-
-
0037422174
-
Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization
-
S. Wessendorf Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization Oncogene 22 2003 1425 1429
-
(2003)
Oncogene
, vol.22
, pp. 1425-1429
-
-
Wessendorf, S.1
-
19
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
A.J. Iafrate Detection of large-scale variation in the human genome Nat. Genet. 36 2004 949 951
-
(2004)
Nat. Genet.
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
-
20
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
J. Sebat Large-scale copy number polymorphism in the human genome Science 305 2004 525 528
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
-
21
-
-
19444365471
-
Exon Array-CGH: Detection of copy number changes of individual exons in human disease
-
(in press)
-
Dhami, P. et al. Exon Array-CGH: detection of copy number changes of individual exons in human disease Genes. Am. J. Hum. Genet. (in press)
-
Genes. Am. J. Hum. Genet.
-
-
Dhami, P.1
-
22
-
-
18144445946
-
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications
-
P.G. Buckley A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications Hum. Mol. Genet. 11 2002 3221 3229
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3221-3229
-
-
Buckley, P.G.1
-
23
-
-
0041867866
-
Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection
-
K.K. Mantripragada Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection J. Mol. Med. 81 2003 443 451
-
(2003)
J. Mol. Med.
, vol.81
, pp. 443-451
-
-
Mantripragada, K.K.1
-
24
-
-
0033805156
-
Mammalian class theta GST and differential susceptibility to carcinogens: A review
-
S. Landi Mammalian class theta GST and differential susceptibility to carcinogens: a review Mutat. Res. 463 2000 247 283
-
(2000)
Mutat. Res.
, vol.463
, pp. 247-283
-
-
Landi, S.1
-
25
-
-
10744233914
-
A tiling resolution DNA microarray with complete coverage of the human genome
-
A.S. Ishkanian A tiling resolution DNA microarray with complete coverage of the human genome Nat. Genet. 36 2004 299 303
-
(2004)
Nat. Genet.
, vol.36
, pp. 299-303
-
-
Ishkanian, A.S.1
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