-
1
-
-
56049102822
-
Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005
-
[PubMed: 18657826]
-
Reller MD, Strickland MJ, Riehle-Colarusso T, Mahle WT, Correa A. Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005. J Pediatr. 2008; 153:807-813. [PubMed: 18657826]
-
(2008)
J Pediatr
, vol.153
, pp. 807-813
-
-
Reller, M.D.1
Strickland, M.J.2
Riehle-Colarusso, T.3
Mahle, W.T.4
Correa, A.5
-
2
-
-
23944516039
-
The bicuspid aortic valve
-
[PubMed: 16129122]
-
Braverman AC, Güven H, Beardslee MA, Makan M, Kates AM, Moon MR. The bicuspid aortic valve. Curr Probl Cardiol. 2005; 30:470-522. [PubMed: 16129122]
-
(2005)
Curr Probl Cardiol
, vol.30
, pp. 470-522
-
-
Braverman, A.C.1
Güven, H.2
Beardslee, M.A.3
Makan, M.4
Kates, A.M.5
Moon, M.R.6
-
3
-
-
33750476343
-
Racial differences in infant mortality attributable to birth defects in the United States, 1989-2002
-
[PubMed 17022030]
-
Yang Q, Chen H, Correa A, Devine O, Mathews TJ, Honein MA. Racial differences in infant mortality attributable to birth defects in the United States, 1989-2002. Birth Defects Res Part A Clin Mol Teratol. 2006; 76:706-713. [PubMed: 17022030]
-
(2006)
Birth Defects Res Part A Clin Mol Teratol.
, vol.76
, pp. 706-713
-
-
Yang, Q.1
Chen, H.2
Correa, A.3
Devine, O.4
Mathews, T.J.5
Honein, M.A.6
-
4
-
-
76749153747
-
20-year survival of children born with congenital anomalies: A population-based study
-
[PubMed: 20092884]
-
Tennant PW, Pearce MS, Bythell M, Rankin J. 20-year survival of children born with congenital anomalies: a population-based study. Lancet. 2010; 375:649-656. [PubMed: 20092884]
-
(2010)
Lancet
, vol.375
, pp. 649-656
-
-
Tennant, P.W.1
Pearce, M.S.2
Bythell, M.3
Rankin, J.4
-
5
-
-
32644442058
-
National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease. Report of the National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease
-
[PubMed 16487831]
-
Williams RG, Pearson GD, Barst RJ, Child JS, del Nido P, Gersony WM, Kuehl KS, Landzberg MJ, Myerson M, Neish SR, Sahn DJ, Verstappen A, Warnes CA, Webb CL. National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease. Report of the National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease. J Am Coll Cardiol. 2006; 47:701-707. [PubMed: 16487831]
-
(2006)
J Am Coll Cardiol.
, vol.47
, pp. 701-707
-
-
Williams, R.G.1
Pearson, G.D.2
Barst, R.J.3
Child, J.S.4
Del Nido, P.5
Gersony, W.M.6
Kuehl, K.S.7
Landzberg, M.J.8
Myerson, M.9
Neish, S.R.10
Sahn, D.J.11
Verstappen, A.12
Warnes, C.A.13
Webb, C.L.14
-
6
-
-
0014334454
-
Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction
-
[PubMed: 4876982]
-
Nora JJ. Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction. Circulation. 1968; 38:604-617. [PubMed: 4876982]
-
(1968)
Circulation
, vol.38
, pp. 604-617
-
-
Nora, J.J.1
-
7
-
-
0020440524
-
Pregnancy and its outcome in women with and without surgical treatment of congenital heart disease
-
[PubMed: 7113941]
-
Whittemore R, Hobbins JC, Engle MA. Pregnancy and its outcome in women with and without surgical treatment of congenital heart disease. Am J Cardiol. 1982; 50:641-651. [PubMed: 7113941]
-
(1982)
Am J Cardiol.
, vol.50
, pp. 641-651
-
-
Whittemore, R.1
Hobbins, J.C.2
Engle, M.A.3
-
8
-
-
68249099670
-
Recurrence of congenital heart defects in families
-
[PubMed: 19597048]
-
Øyen N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PK, Melbye M. Recurrence of congenital heart defects in families. Circulation. 2009; 120:295-301. [PubMed: 19597048]
-
(2009)
Circulation
, vol.120
, pp. 295-301
-
-
Øyen, N.1
Poulsen, G.2
Boyd, H.A.3
Wohlfahrt, J.4
Jensen, P.K.5
Melbye, M.6
-
9
-
-
3242764513
-
Bicuspid aortic valve is heritable
-
[PubMed: 15234422]
-
Cripe L, Andelfinger G, Martin LJ, Shooner K, Benson DW. Bicuspid aortic valve is heritable. J Am Coll Cardiol. 2004; 44:138-143. [PubMed: 15234422]
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 138-143
-
-
Cripe, L.1
Andelfinger, G.2
Martin, L.J.3
Shooner, K.4
Benson, D.W.5
-
10
-
-
34948833712
-
Hypoplastic left heart syndrome is heritable
-
[PubMed: 17936159]
-
Hinton RB Jr, Martin LJ, Tabangin ME, Mazwi ML, Cripe LH, Benson DW. Hypoplastic left heart syndrome is heritable. J Am Coll Cardiol. 2007; 50:1590-1595. [PubMed: 17936159]
-
(2007)
J Am Coll Cardiol
, vol.50
, pp. 1590-1595
-
-
Hinton Jr., R.B.1
Martin, L.J.2
Tabangin, M.E.3
Mazwi, M.L.4
Cripe, L.H.5
Benson, D.W.6
-
11
-
-
20144388158
-
Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability
-
[PubMed: 15690347]
-
McBride KL, Pignatelli R, Lewin M, Ho T, Fernbach S, Menesses A, Lam W, Leal SM, Kaplan N, Schliekelman P, Towbin JA, Belmont JW. Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability. Am J Med Genet A. 2005; 134A:180-186. [PubMed: 15690347]
-
(2005)
Am J Med Genet A
, vol.134 A
, pp. 180-186
-
-
McBride, K.L.1
Pignatelli, R.2
Lewin, M.3
Ho, T.4
Fernbach, S.5
Menesses, A.6
Lam, W.7
Leal, S.M.8
Kaplan, N.9
Schliekelman, P.10
Towbin, J.A.11
Belmont, J.W.12
-
12
-
-
0041825408
-
Parental consanguinity and congenital heart malformations in a developing country
-
[PubMed: 12522788]
-
Nabulsi MM, Tamim H, Sabbagh M, Obeid MY, Yunis KA, Bitar FF. Parental consanguinity and congenital heart malformations in a developing country. Am J Med Genet A. 2003; 116A:342- 347. [PubMed: 12522788]
-
(2003)
Am J Med Genet A.
, vol.116 A
, pp. 342-347
-
-
Nabulsi, M.M.1
Tamim, H.2
Sabbagh, M.3
Obeid, M.Y.4
Yunis, K.A.5
Bitar, F.F.6
-
13
-
-
33745610099
-
Consanguineous marriage and congenital heart defects: A case-control study in the neonatal period
-
[PubMed: 16763961]
-
Yunis K, Khalid Y, Mumtaz G, et al. Consanguineous marriage and congenital heart defects: a case-control study in the neonatal period. Am J Med Genet A. 2006; 140:1524-1530. [PubMed: 16763961]
-
(2006)
Am J Med Genet A.
, vol.140
, pp. 1524-1530
-
-
Yunis, K.1
Khalid, Y.2
Mumtaz, G.3
-
14
-
-
17444434198
-
Frequency of 22q11 deletions in patients with conotruncal defects
-
[PubMed: 9708481]
-
Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA. Frequency of 22q11 deletions in patients with conotruncal defects. J Am Coll Cardiol. 1998; 32:492-498. [PubMed: 9708481]
-
(1998)
J Am Coll Cardiol
, vol.32
, pp. 492-498
-
-
Goldmuntz, E.1
Clark, B.J.2
Mitchell, L.E.3
Jawad, A.F.4
Cuneo, B.F.5
Reed, L.6
McDonald-Mcginn, D.7
Chien, P.8
Feuer, J.9
Zackai, E.H.10
Emanuel, B.S.11
Driscoll, D.A.12
-
15
-
-
34249000299
-
Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients
-
[PubMed: 17384091]
-
Thienpont B, Mertens L, de Ravel T, Eyskens B, Boshoff D, Maas N, Fryns JP, Gewillig M, Vermeesch JR, Devriendt K. Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients. Eur Heart J. 2007; 28:2778- 2784. [PubMed: 17384091]
-
(2007)
Eur Heart J
, vol.28
, pp. 2778-2784
-
-
Thienpont, B.1
Mertens, L.2
De Ravel, T.3
Eyskens, B.4
Boshoff, D.5
Maas, N.6
Fryns, J.P.7
Gewillig, M.8
Vermeesch, J.R.9
Devriendt, K.10
-
16
-
-
55049097760
-
Cryptic chromosomal abnormalities identified in children with congenital heart disease
-
[PubMed: 18535492]
-
Richards AA, Santos LJ, Nichols HA, Crider BP, Elder FF, Hauser NS, Zinn AR, Garg V. Cryptic chromosomal abnormalities identified in children with congenital heart disease. Pediatr Res. 2008; 64:358-363. [PubMed: 18535492]
-
(2008)
Pediatr Res
, vol.64
, pp. 358-363
-
-
Richards, A.A.1
Santos, L.J.2
Nichols, H.A.3
Crider, B.P.4
Elder, F.F.5
Hauser, N.S.6
Zinn, A.R.7
Garg, V.8
-
17
-
-
68149181705
-
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
-
[PubMed: 19597493]
-
Greenway SC, Pereira AC, Lin JC, et al. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. Nat Genet. 2009; 41:931-935. [PubMed: 19597493]
-
(2009)
Nat Genet
, vol.41
, pp. 931-935
-
-
Greenway, S.C.1
Pereira, A.C.2
Lin, J.C.3
-
18
-
-
84866070546
-
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
-
[PubMed: 22939634]
-
Soemedi R, Wilson IJ, Bentham J, et al. Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. Am J Hum Genet. 2012; 91:489-501. [PubMed: 22939634]
-
(2012)
Am J Hum Genet
, vol.91
, pp. 489-501
-
-
Soemedi, R.1
Wilson, I.J.2
Bentham, J.3
-
19
-
-
84866915849
-
Rare copy number variants contribute to congenital left-sided heart disease
-
[PubMed: 22969434]
-
Hitz MP, Lemieux-Perreault LP, Marshall C, et al. Rare copy number variants contribute to congenital left-sided heart disease. PLoS Genet. 2012; 8:e1002903. [PubMed: 22969434]
-
(2012)
PLoS Genet.
, vol.8
-
-
Hitz, M.P.1
Lemieux-Perreault, L.P.2
Marshall, C.3
-
20
-
-
79952584346
-
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
-
[PubMed: 21282601]
-
Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, Khokha MK, Brueckner M. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning. Proc Natl Acad Sci USA. 2011; 108:2915-2920. [PubMed: 21282601]
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 2915-2920
-
-
Fakhro, K.A.1
Choi, M.2
Ware, S.M.3
Belmont, J.W.4
Towbin, J.A.5
Lifton, R.P.6
Khokha, M.K.7
Brueckner, M.8
-
21
-
-
82355170520
-
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies
-
[PubMed: 22010865]
-
Goldmuntz E, Paluru P, Glessner J, Hakonarson H, Biegel JA, White PS, Gai X, Shaikh TH. Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies. Congenit Heart Dis. 2011; 6:592-602. [PubMed: 22010865]
-
(2011)
Congenit Heart Dis.
, vol.6
, pp. 592-602
-
-
Goldmuntz, E.1
Paluru, P.2
Glessner, J.3
Hakonarson, H.4
Biegel, J.A.5
White, P.S.6
Gai, X.7
Shaikh, T.H.8
-
22
-
-
34250305402
-
Genetic basis for congenital heart defects: Current knowledge: A scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: Endorsed by the American Academy of Pediatrics
-
American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young [PubMed: 17519398]
-
Pierpont ME, Basson CT, Benson DW Jr, Gelb BD, Giglia TM, Goldmuntz E, McGee G, Sable CA, Srivastava D, Webb CL. American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young. Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. Circulation. 2007; 115:3015-3038. [PubMed: 17519398]
-
(2007)
Circulation
, vol.115
, pp. 3015-3038
-
-
Pierpont, M.E.1
Basson, C.T.2
Benson Jr., D.W.3
Gelb, B.D.4
Giglia, T.M.5
Goldmuntz, E.6
McGee, G.7
Sable, C.A.8
Srivastava, D.9
Webb, C.L.10
-
23
-
-
84864578044
-
The Good SHP2 Association: A porthole into the genetics of congenital heart disease
-
[PubMed: 22715277]
-
Gelb BD, Seidman CE. The Good SHP2 Association: a porthole into the genetics of congenital heart disease. Circ Cardiovasc Genet. 2012; 5:271-273. [PubMed: 22715277]
-
(2012)
Circ Cardiovasc Genet.
, vol.5
, pp. 271-273
-
-
Gelb, B.D.1
Seidman, C.E.2
-
24
-
-
77949300615
-
The National Heart, Lung, and Blood Institute bench to bassinet program: A new paradigm for translational research
-
[PubMed: 20298934]
-
Kaltman JR, Schramm C, Pearson GD. The National Heart, Lung, and Blood Institute bench to bassinet program: a new paradigm for translational research. J Am Coll Cardiol. 2010; 55:1262- 1265. [PubMed: 20298934]
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 1262-1265
-
-
Kaltman, J.R.1
Schramm, C.2
Pearson, G.D.3
-
25
-
-
79951863517
-
Ethical and practical guidelines for reporting genetic research results to study participants: Updated guidelines from a National Heart, Lung, and Blood Institute working group
-
[PubMed: 21156933]
-
Fabsitz RR, McGuire A, Sharp RR, et al. Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circ Cardiovasc Genet. 2010; 3:574-580. [PubMed: 21156933]
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 574-580
-
-
Fabsitz, R.R.1
McGuire, A.2
Sharp, R.R.3
-
26
-
-
35348837913
-
National Birth Defects Prevention Study. Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies
-
[PubMed: 17729292]
-
Botto LD, Lin AE, Riehle-Colarusso T, Malik S, Correa A. National Birth Defects Prevention Study. Seeking causes: classifying and evaluating congenital heart defects in etiologic studies. Birth Defects Res Part A Clin Mol Teratol. 2007; 79:714-727. [PubMed: 17729292]
-
(2007)
Birth Defects Res Part A Clin Mol Teratol.
, vol.79
, pp. 714-727
-
-
Botto, L.D.1
Lin, A.E.2
Riehle-Colarusso, T.3
Malik, S.4
Correa, A.5
-
27
-
-
60649087124
-
National time trends in congenital heart defects Denmark 1977-2005
-
e461 [PubMed 19249416]
-
Oyen N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PK, Melbye M. National time trends in congenital heart defects, Denmark, 1977-2005. Am Heart J. 2009; 157:467-473. e461. [PubMed: 19249416]
-
(2009)
Am Heart J.
, vol.157
, pp. 467-473
-
-
Oyen, N.1
Poulsen, G.2
Boyd, H.A.3
Wohlfahrt, J.4
Jensen, P.K.5
Melbye, M.6
-
28
-
-
84867280219
-
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth
-
[PubMed: 23040492]
-
Fromer M, Moran JL, Chambert K, Banks E, Bergen SE, Ruderfer DM, Handsaker RE, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, Sullivan PF, Hultman CM, Sklar P, Purcell SM. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. Am J Hum Genet. 2012; 91:597-607. [PubMed: 23040492]
-
(2012)
Am J Hum Genet.
, vol.91
, pp. 597-607
-
-
Fromer, M.1
Moran, J.L.2
Chambert, K.3
Banks, E.4
Bergen, S.E.5
Ruderfer, D.M.6
Handsaker, R.E.7
McCarroll, S.A.8
O'Donovan, M.C.9
Owen, M.J.10
Kirov, G.11
Sullivan, P.F.12
Hultman, C.M.13
Sklar, P.14
Purcell, S.M.15
-
29
-
-
84864609288
-
NHLBI Exome Sequencing Project. Copy number variation detection and genotyping from exome sequence data
-
[PubMed: 22585873]
-
Krumm N, Sudmant PH, Ko A, O'Roak BJ, Malig M, Coe BP, Quinlan AR, Nickerson DA, Eichler EE. NHLBI Exome Sequencing Project. Copy number variation detection and genotyping from exome sequence data. Genome Res. 2012; 22:1525-1532. [PubMed: 22585873]
-
(2012)
Genome Res
, vol.22
, pp. 1525-1532
-
-
Krumm, N.1
Sudmant, P.H.2
Ko, A.3
O'Roak, B.J.4
Malig, M.5
Coe, B.P.6
Quinlan, A.R.7
Nickerson, D.A.8
Eichler, E.E.9
-
30
-
-
0041845296
-
Cilia are at the heart of vertebrate left-right asymmetry
-
[PubMed: 12888012]
-
McGrath J, Brueckner M. Cilia are at the heart of vertebrate left-right asymmetry. Curr Opin Genet Dev. 2003; 13:385-392. [PubMed: 12888012]
-
(2003)
Curr Opin Genet Dev
, vol.13
, pp. 385-392
-
-
McGrath, J.1
Brueckner, M.2
-
31
-
-
70449670932
-
Disorders of left-right asymmetry: Heterotaxy and situs inversus
-
[PubMed: 19876930]
-
Sutherland MJ, Ware SM. Disorders of left-right asymmetry: heterotaxy and situs inversus. Am J Med Genet C Semin Med Genet. 2009; 151C:307-317. [PubMed: 19876930]
-
(2009)
Am J Med Genet C Semin Med Genet.
, vol.151 C
, pp. 307-317
-
-
Sutherland, M.J.1
Ware, S.M.2
-
32
-
-
4444298928
-
Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease
-
[PubMed: 15342699]
-
Reamon-Buettner SM, Borlak J. Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease. J Med Genet. 2004; 41:684-690. [PubMed: 15342699]
-
(2004)
J Med Genet
, vol.41
, pp. 684-690
-
-
Reamon-Buettner, S.M.1
Borlak, J.2
-
33
-
-
7244238119
-
TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts
-
[PubMed: 15221798]
-
Reamon-Buettner SM, Borlak J. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts. Hum Mutat. 2004; 24:104. [PubMed: 15221798]
-
(2004)
Hum Mutat
, vol.24
, pp. 104
-
-
Reamon-Buettner, S.M.1
Borlak, J.2
-
34
-
-
34548094528
-
HEY2 mutations in malformed hearts
-
[PubMed: 16329098]
-
Reamon-Buettner SM, Borlak J. HEY2 mutations in malformed hearts. Hum Mutat. 2006; 27:118. [PubMed: 16329098]
-
(2006)
Hum Mutat
, vol.27
, pp. 118
-
-
Reamon-Buettner, S.M.1
Borlak, J.2
-
35
-
-
2442705544
-
Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations
-
[PubMed: 15161646]
-
Reamon-Buettner SM, Hecker H, Spanel-Borowski K, Craatz S, Kuenzel E, Borlak J. Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations. Am J Pathol. 2004; 164:2117-2125. [PubMed: 15161646]
-
(2004)
Am J Pathol
, vol.164
, pp. 2117-2125
-
-
Reamon-Buettner, S.M.1
Hecker, H.2
Spanel-Borowski, K.3
Craatz, S.4
Kuenzel, E.5
Borlak, J.6
-
36
-
-
33646548928
-
Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease
-
[PubMed: 16711160]
-
Reamon-Buettner SM, Spanel-Borowski K, Borlak J. Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease. Ann Anat. 2006; 188:213-220. [PubMed: 16711160]
-
(2006)
Ann Anat
, vol.188
, pp. 213-220
-
-
Reamon-Buettner, S.M.1
Spanel-Borowski, K.2
Borlak, J.3
-
37
-
-
80053124071
-
Somatic mutations in NKX2-5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart
-
[PubMed: 22043484]
-
Esposito G, Butler TL, Blue GM, Cole AD, Sholler GF, Kirk EP, Grossfeld P, Perryman BM, Harvey RP, Winlaw DS. Somatic mutations in NKX2-5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart. Am J Med Genet A. 2011; 155A:2416-2421. [PubMed: 22043484]
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 2416-2421
-
-
Esposito, G.1
Butler, T.L.2
Blue, G.M.3
Cole, A.D.4
Sholler, G.F.5
Kirk, E.P.6
Grossfeld, P.7
Perryman, B.M.8
Harvey, R.P.9
Winlaw, D.S.10
-
38
-
-
55449120805
-
Genetic mapping in human disease
-
[PubMed: 18988837]
-
Altshuler D, Daly MJ, Lander ES. Genetic mapping in human disease. Science. 2008; 322:881-888. [PubMed: 18988837]
-
(2008)
Science
, vol.322
, pp. 881-888
-
-
Altshuler, D.1
Daly, M.J.2
Lander, E.S.3
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