-
1
-
-
0037439356
-
Cancer in Fanconi anemia, 1927-2001
-
DOI 10.1002/cncr.11046
-
BP Alter 2003 Cancer in Fanconi anemia, 1927-2001 Cancer 97 425 440 10.1002/cncr.11046 10.1002/cncr.11046 12518367 (Pubitemid 36133810)
-
(2003)
Cancer
, vol.97
, Issue.2
, pp. 425-440
-
-
Alter, B.P.1
-
2
-
-
0033740880
-
Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group
-
Anglian Breast Cancer Study Group. 10.1054/bjoc.2000.1407 10.1054/bjoc.2000.1407
-
Anglian Breast Cancer Study Group 2000 Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group Br J Cancer 83 1301 1308 10.1054/bjoc.2000. 1407 10.1054/bjoc.2000.1407
-
(2000)
Br J Cancer
, vol.83
, pp. 1301-1308
-
-
-
3
-
-
25144503943
-
The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair
-
DOI 10.1038/ng1627, PII NG1627
-
WL Bridge CJ Vandenberg RJ Franklin, et al. 2005 The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair Nat Genet 37 953 957 10.1038/ng1627 10.1038/ng1627 1:CAS:528: DC%2BD2MXpsFWisbs%3D 16116421 (Pubitemid 43086151)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, pp. 953-957
-
-
Bridge, W.L.1
Vandenberg, C.J.2
Franklin, R.J.3
Hiom, K.4
-
4
-
-
61449204036
-
The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives
-
10.1007/s10549-008-0036-z 10.1007/s10549-008-0036-z 1:CAS:528: DC%2BD1MXisFSqt7o%3D 18446436
-
AY Cao J Huang Z Hu, et al. 2009 The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives Breast Cancer Res Treat 114 457 462 10.1007/s10549-008- 0036-z 10.1007/s10549-008-0036-z 1:CAS:528:DC%2BD1MXisFSqt7o%3D 18446436
-
(2009)
Breast Cancer Res Treat
, vol.114
, pp. 457-462
-
-
Cao, A.Y.1
Huang, J.2
Hu, Z.3
-
5
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
DOI 10.1038/nature05609, PII NATURE05609
-
H Erkko B Xia J Nikkila, et al. 2007 A recurrent mutation in PALB2 in Finnish cancer families Nature 446 316 319 10.1038/nature05609 10.1038/nature05609 1:CAS:528:DC%2BD2sXivVSns78%3D 17287723 (Pubitemid 46426155)
-
(2007)
Nature
, vol.446
, Issue.7133
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
Schleutker, J.4
Syrjakoski, K.5
Mannermaa, A.6
Kallioniemi, A.7
Pylkas, K.8
Karppinen, S.-M.9
Rapakko, K.10
Miron, A.11
Sheng, Q.12
Li, G.13
Mattila, H.14
Bell, D.W.15
Haber, D.A.16
Grip, M.17
Reiman, M.18
Jukkola-Vuorinen, A.19
Mustonen, A.20
Kere, J.21
Aaltonen, L.A.22
Kosma, V.-M.23
Kataja, V.24
Soini, Y.25
Drapkin, R.I.26
Livingston, D.M.27
Winqvist, R.28
more..
-
6
-
-
40349111045
-
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women
-
10.1186/bcr1828 10.1186/bcr1828 18053174
-
WD Foulkes P Ghadirian MR Akbari, et al. 2007 Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women Breast Cancer Res 9 R83 10.1186/bcr1828 10.1186/bcr1828 18053174
-
(2007)
Breast Cancer Res
, vol.9
, pp. 83
-
-
Foulkes, W.D.1
Ghadirian, P.2
Akbari, M.R.3
-
7
-
-
58549086980
-
Analysis of FANCB and FANCN/PALB2 Fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families
-
10.1007/s10549-008-9945-0 10.1007/s10549-008-9945-0 18302019
-
MJ Garcia V Fernandez A Osorio, et al. 2008 Analysis of FANCB and FANCN/PALB2 Fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families Breast Cancer Res Treat 113 545 551 10.1007/s10549-008-9945-0 10.1007/s10549-008-9945-0 18302019
-
(2008)
Breast Cancer Res Treat
, vol.113
, pp. 545-551
-
-
Garcia, M.J.1
Fernandez, V.2
Osorio, A.3
-
8
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
10.1053/gast.2000.20228 10.1053/gast.2000.20228 1:STN:280: DC%2BD3M%2Fnt1ersw%3D%3D 11113065
-
FM Giardiello JD Brensinger AC Tersmette, et al. 2000 Very high risk of cancer in familial Peutz-Jeghers syndrome Gastroenterology 119 1447 1453 10.1053/gast.2000.20228 10.1053/gast.2000.20228 1:STN:280: DC%2BD3M%2Fnt1ersw%3D%3D 11113065
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
-
9
-
-
48449091498
-
Evidence against PALB2 involvement in Icelandic breast cancer susceptibility
-
10.1186/1477-5751-7-5 10.1186/1477-5751-7-5 18637200
-
H Gunnarsson A Arason EM Gillanders, et al. 2008 Evidence against PALB2 involvement in Icelandic breast cancer susceptibility J Negat Results Biomed 7 5 10.1186/1477-5751-7-5 10.1186/1477-5751-7-5 18637200
-
(2008)
J Negat Results Biomed
, vol.7
, pp. 5
-
-
Gunnarsson, H.1
Arason, A.2
Gillanders, E.M.3
-
10
-
-
0042519602
-
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice
-
DOI 10.1101/gad.1103403
-
S Houghtaling C Timmers M Noll, et al. 2003 Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice Genes Dev 17 2021 2035 10.1101/gad.1103403 10.1101/gad.1103403 1:CAS:528:DC%2BD3sXms1Kntr0%3D 12893777 (Pubitemid 36999328)
-
(2003)
Genes and Development
, vol.17
, Issue.16
, pp. 2021-2035
-
-
Houghtaling, S.1
Timmers, C.2
Noll, M.3
Finegold, M.J.4
Jones, S.N.5
Stephen Meyn, M.6
Grompe, M.7
-
11
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
DOI 10.1126/science.1073834
-
NG Howlett T Taniguchi S Olson, et al. 2002 Biallelic inactivation of BRCA2 in Fanconi anemia Science 297 606 609 10.1126/science.1073834 10.1126/science.1073834 1:CAS:528:DC%2BD38XlslWrs7k%3D 12065746 (Pubitemid 34815345)
-
(2002)
Science
, vol.297
, Issue.5581
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
Cox, B.4
Waisfisz, Q.5
De Die-Smulders, C.6
Persky, N.7
Grompe, M.8
Joenje, H.9
Pals, G.10
Ikeda, H.11
Fox, E.A.12
D'Andrea, A.D.13
-
12
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
DOI 10.1038/ng1625, PII NG1625
-
M Levitus Q Waisfisz BC Godthelp, et al. 2005 The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J Nat Genet 37 934 935 10.1038/ng1625 10.1038/ng1625 1:CAS:528:DC%2BD2MXpsFWisb0%3D 16116423 (Pubitemid 43086148)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
De Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Rooimans, M.A.9
Pals, G.10
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
13
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
DOI 10.1038/ng1624, PII NG1624
-
O Levran C Attwooll RT Henry, et al. 2005 The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia Nat Genet 37 931 933 10.1038/ng1624 10.1038/ng1624 1:CAS:528:DC%2BD2MXpsFWisbw%3D 16116424 (Pubitemid 43086147)
-
(2005)
Nature Genetics
, vol.37
, Issue.9
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
Milton, K.L.4
Neveling, K.5
Rio, P.6
Batish, S.D.7
Kalb, R.8
Velleuer, E.9
Barral, S.10
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
14
-
-
34447619477
-
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
-
10.1186/bcr1336 10.1186/bcr1336 1:CAS:528:DC%2BD2MXht1WmsrjL 16280053
-
AG Lewis J Flanagan A Marsh, et al. 2005 Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer Breast Cancer Res 7 R1005 R1016 10.1186/bcr1336 10.1186/bcr1336 1:CAS:528:DC%2BD2MXht1WmsrjL 16280053
-
(2005)
Breast Cancer Res
, vol.7
-
-
Lewis, A.G.1
Flanagan, J.2
Marsh, A.3
-
15
-
-
17344363637
-
Inherited mutations in PTEN that are associated with breast cancer, Cowden disease, and juvenile polyposis
-
DOI 10.1086/301639
-
ED Lynch EA Ostermeyer MK Lee, et al. 1997 Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis Am J Hum Genet 61 1254 1260 10.1086/301639 10.1086/301639 1:CAS:528: DyaK1cXntVKltQ%3D%3D 9399897 (Pubitemid 28046900)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.6
, pp. 1254-1260
-
-
Lynch, E.D.1
Ostermeyer, E.A.2
Lee, M.K.3
Arena, J.F.4
Ji, H.5
Dann, J.6
Swisshelm, K.7
Suchard, D.8
MacLeod, P.M.9
Kvinnsland, S.10
Gjertsen, B.T.11
Heimdal, K.12
Lubs, H.13
Moller, P.14
King, M.-C.15
-
16
-
-
0025633582
-
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
-
10.1126/science.1978757 10.1126/science.1978757 1:CAS:528: DyaK3MXjslSisw%3D%3D 1978757
-
D Malkin FP Li LC Strong, et al. 1990 Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms Science 250 1233 1238 10.1126/science.1978757 10.1126/science.1978757 1:CAS:528: DyaK3MXjslSisw%3D%3D 1978757
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Strong, L.C.3
-
17
-
-
33749023325
-
Fanconi anaemia genes and susceptibility to cancer
-
DOI 10.1038/sj.onc.1209878, PII 1209878
-
CG Mathew 2006 Fanconi anaemia genes and susceptibility to cancer Oncogene 25 5875 5884 10.1038/sj.onc.1209878 10.1038/sj.onc.1209878 1:CAS:528:DC%2BD28XhtVSgurjI 16998502 (Pubitemid 44453443)
-
(2006)
Oncogene
, vol.25
, Issue.43
, pp. 5875-5884
-
-
Mathew, C.G.1
-
18
-
-
34249811785
-
The 13th Fanconi anemia gene identified: FANCI-importance of the 'Fanconi anemia pathway' for cellular oncology
-
1:CAS:528:DC%2BD2sXksVCjtrg%3D 17452769
-
GA Meijer 2007 The 13th Fanconi anemia gene identified: FANCI-importance of the 'Fanconi anemia pathway' for cellular oncology Cell Oncol 29 181 182 1:CAS:528:DC%2BD2sXksVCjtrg%3D 17452769
-
(2007)
Cell Oncol
, vol.29
, pp. 181-182
-
-
Meijer, G.A.1
-
19
-
-
34250889566
-
Genetic susceptibility for breast cancer: How many more genes to be found?
-
DOI 10.1016/j.critrevonc.2006.12.004, PII S1040842806002496
-
RA Oldenburg H Meijers-Heijboer CJ Cornelisse, et al. 2007 Genetic susceptibility for breast cancer: how many more genes to be found? Crit Rev Oncol Hematol 63 125 149 10.1016/j.critrevonc.2006.12.004 10.1016/j.critrevonc. 2006.12.004 1:STN:280:DC%2BD2szoslKhtg%3D%3D 17498966 (Pubitemid 46990913)
-
(2007)
Critical Reviews in Oncology/Hematology
, vol.63
, Issue.2
, pp. 125-149
-
-
Oldenburg, R.A.1
Meijers-Heijboer, H.2
Cornelisse, C.J.3
Devilee, P.4
-
20
-
-
44949248224
-
Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families
-
DOI 10.1186/1471-2407-8-146
-
K Pylkas H Erkko J Nikkila, et al. 2008 Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families BMC Cancer 8 146 10.1186/1471-2407-8-146 10.1186/1471-2407-8-146 18501021 (Pubitemid 351803800)
-
(2008)
BMC Cancer
, vol.8
, pp. 146
-
-
Pylkas, K.1
Erkko, H.2
Nikkila, J.3
Solyom, S.4
Winqvist, R.5
-
21
-
-
34547785606
-
Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: New lessons from old players
-
DOI 10.1093/hmg/ddm026, Cancer Genetics
-
N Rahman RH Scott 2007 Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players Hum Mol Genet 16 60 66 10.1093/hmg/ddm026 Spec No 1: (Pubitemid 47241843)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.R1
-
-
Rahman, N.1
Scott, R.H.2
-
22
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
DOI 10.1038/ng1959, PII NG1959
-
N Rahman S Seal D Thompson, et al. 2007 PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Nat Genet 39 165 167 10.1038/ng1959 10.1038/ng1959 1:CAS:528:DC%2BD2sXpvFeqsw%3D%3D 17200668 (Pubitemid 46184346)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
23
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
DOI 10.1038/ng1947, PII NG1947
-
S Reid D Schindler H Hanenberg, et al. 2007 Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer Nat Genet 39 162 164 10.1038/ng1947 10.1038/ng1947 1:CAS:528:DC%2BD2sXpvFersA%3D%3D 17200671 (Pubitemid 46184345)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
Neveling, K.7
Kelly, P.8
Seal, S.9
Freund, M.10
Wurm, M.11
Batish, S.D.12
Lach, F.P.13
Yetgin, S.14
Neitzel, H.15
Ariffin, H.16
Tischkowitz, M.17
Mathew, C.G.18
Auerbach, A.D.19
Rahman, N.20
more..
-
24
-
-
33746491583
-
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
-
DOI 10.1038/ng1837, PII NG1837
-
AD Renwick S Thompson P Seal, et al. 2006 ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles Nat Genet 38 873 875 10.1038/ng1837 10.1038/ng1837 1:CAS:528:DC%2BD28XnsVChu7Y%3D 16832357 (Pubitemid 44141653)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
Kelly, P.4
Chagtai, T.5
Ahmed, M.6
North, B.7
Jayatilake, H.8
Barfoot, R.9
Spanova, K.10
McGuffog, L.11
Evans, D.G.12
Eccles, D.13
Easton, D.F.14
Stratton, M.R.15
Rahman, N.16
-
25
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
-
10.1093/nar/gnf056 10.1093/nar/gnf056 12060695
-
JP Schouten CJ McElgunn R Waaijer, et al. 2002 Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification Nucleic Acids Res 30 e57 10.1093/nar/gnf056 10.1093/nar/gnf056 12060695
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 57
-
-
Schouten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
-
26
-
-
9144268932
-
Evaluation of Fanconi anemia genes in familial breast cancer predisposition
-
1:CAS:528:DC%2BD3sXhtVSqtLjM 14695169
-
S Seal R Barfoot H Jayatilake, et al. 2003 Evaluation of Fanconi anemia genes in familial breast cancer predisposition Cancer Res 63 8596 8599 1:CAS:528:DC%2BD3sXhtVSqtLjM 14695169
-
(2003)
Cancer Res
, vol.63
, pp. 8596-8599
-
-
Seal, S.1
Barfoot, R.2
Jayatilake, H.3
-
27
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
DOI 10.1038/ng1902, PII NG1902
-
S Seal D Thompson A Renwick, et al. 2006 Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles Nat Genet 38 1239 1241 10.1038/ng1902 10.1038/ng1902 1:CAS:528:DC%2BD28XhtFeisbjJ 17033622 (Pubitemid 44646283)
-
(2006)
Nature Genetics
, vol.38
, Issue.11
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
28
-
-
3042582651
-
CHEK2 1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
-
DOI 10.1086/421251
-
The CHEK2 Breast Cancer Case-Control Consortium 2004 CHEK2 1100delC and susceptibility to breast cancer: a collaborative analysis involving 10, 860 breast cancer cases and 9, 065 controls from 10 studies Am J Hum Genet 74 1175 1182 10.1086/421251 10.1086/421251 (Pubitemid 38669316)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.6
, pp. 1175-1182
-
-
Easton, D.1
-
29
-
-
42949174531
-
Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer
-
DOI 10.1002/pros.20729
-
M Tischkowitz N Sabbaghian AM Ray, et al. 2008 Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer Prostate 68 675 678 10.1002/pros.20729 10.1002/pros.20729 18288683 (Pubitemid 351614645)
-
(2008)
Prostate
, vol.68
, Issue.6
, pp. 675-678
-
-
Tischkowitz, M.1
Sabbaghian, N.2
Ray, A.M.3
Lange, E.M.4
Foulkes, W.D.5
Cooney, K.A.6
-
30
-
-
33745728357
-
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: Application in a Dutch cancer clinic setting
-
10.1002/humu.20340 10.1002/humu.20340 16683254
-
AH Van der Hout AM van den Ouweland RB van der Luijt, et al. 2006 A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting Hum Mutat 27 654 666 10.1002/humu.20340 10.1002/humu.20340 16683254
-
(2006)
Hum Mutat
, vol.27
, pp. 654-666
-
-
Van Der Hout, A.H.1
Van Den Ouweland, A.M.2
Van Der Luijt, R.B.3
-
31
-
-
34548759123
-
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
-
DOI 10.1038/nrg2159, PII NRG2159
-
W Wang 2007 Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins Nat Rev Genet 8 735 748 10.1038/nrg2159 10.1038/nrg2159 1:CAS:528:DC%2BD2sXhtVCrsb3J 17768402 (Pubitemid 47429206)
-
(2007)
Nature Reviews Genetics
, vol.8
, Issue.10
, pp. 735-748
-
-
Wang, W.1
-
32
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
DOI 10.1038/ng1942, PII NG1942
-
B Xia JC Dorsman N Ameziane, et al. 2007 Fanconi anemia is associated with a defect in the BRCA2 partner PALB2 Nat Genet 39 159 161 10.1038/ng1942 10.1038/ng1942 1:CAS:528:DC%2BD2sXpvFekug%3D%3D 17200672 (Pubitemid 46184344)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
De Vries, Y.4
Rooimans, M.A.5
Sheng, Q.6
Pals, G.7
Errami, A.8
Gluckman, E.9
Llera, J.10
Wang, W.11
Livingston, D.M.12
Joenje, H.13
De Winter, J.P.14
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