-
1
-
-
36448995027
-
Genetic predisposition to respiratory diseases: Infiltrative lung diseases
-
Steele MP, Brown KK. Genetic predisposition to respiratory diseases: infiltrative lung diseases. Respiration. 2007;74:601-608.
-
(2007)
Respiration.
, vol.74
, pp. 601-608
-
-
Steele, M.P.1
Brown, K.K.2
-
2
-
-
85205940719
-
Idiopathic pulmonary fibrosis: Diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS)
-
Society AT. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS). Am J Respir Crit Care Med. 2000;161:646-664.
-
(2000)
Am J Respir Crit Care Med.
, vol.161
, pp. 646-664
-
-
Society, A.T.1
-
3
-
-
0037080547
-
American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001
-
American Thoracic S and European Respiratory S.
-
American Thoracic S and European Respiratory S. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. Am J Respir Crit Care Med. 2002;165:277-304.
-
(2002)
Am J Respir Crit Care Med.
, vol.165
, pp. 277-304
-
-
-
4
-
-
79952717349
-
An official ATS/ERS/JRS/ALAT statement: Idiopathic pulmonary fibrosis: Evidence-based guidelines for diagnosis and management
-
Raghu G, Collard HR, Egan JJ, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011;183:788-824.
-
(2011)
Am J Respir Crit Care Med.
, vol.183
, pp. 788-824
-
-
Raghu, G.1
Collard, H.R.2
Egan, J.J.3
-
5
-
-
0021889048
-
The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations
-
DePinho RA, Kaplan KL. The Hermansky-Pudlak syndrome. Report of three cases and review of pathophysiology and management considerations. Medicine (Baltimore). 1985;64:192-202.
-
(1985)
Medicine (Baltimore).
, vol.64
, pp. 192-202
-
-
Depinho, R.A.1
Kaplan, K.L.2
-
6
-
-
0019834061
-
Von Recklinghausen neurofibromatosis
-
Riccardi VM. Von Recklinghausen neurofibromatosis. N Engl J Med. 1981;305:1617-1627.
-
(1981)
N Engl J Med.
, vol.305
, pp. 1617-1627
-
-
Riccardi, V.M.1
-
7
-
-
0017754442
-
Severe pulmonary involvement in adult Gaucher's disease. Report of three cases and review of the literature
-
Schneider EL, Epstein CJ, Kaback MJ, et al. Severe pulmonary involvement in adult Gaucher's disease. Report of three cases and review of the literature. Am J Med. 1977;63:475-480.
-
(1977)
Am J Med.
, vol.63
, pp. 475-480
-
-
Schneider, E.L.1
Epstein, C.J.2
Kaback, M.J.3
-
8
-
-
0021921193
-
Defective host defence mechanisms in a family with hypocalciuric hypercalcaemia and coexisting interstitial lung disease
-
Auwerx J, Boogaerts M, Ceuppens JL, et al. Defective host defence mechanisms in a family with hypocalciuric hypercalcaemia and coexisting interstitial lung disease. Clin Exp Immunol. 1985;62:57-64.
-
(1985)
Clin Exp Immunol.
, vol.62
, pp. 57-64
-
-
Auwerx, J.1
Boogaerts, M.2
Ceuppens, J.L.3
-
9
-
-
0014576399
-
The pathophysiology of the lungs in tuberous sclerosis. A case report and literature review
-
Harris JO, Waltuck BL, Swenson EW. The pathophysiology of the lungs in tuberous sclerosis. A case report and literature review. Am Rev Respir Dis. 1969;100:379-387.
-
(1969)
Am Rev Respir Dis.
, vol.100
, pp. 379-387
-
-
Harris, J.O.1
Waltuck, B.L.2
Swenson, E.W.3
-
10
-
-
0033754823
-
Dyskeratosis congenita in all its forms
-
Dokal I. Dyskeratosis congenita in all its forms. Br J Haematol. 2000;110:768-779.
-
(2000)
Br J Haematol.
, vol.110
, pp. 768-779
-
-
Dokal, I.1
-
11
-
-
0018650787
-
Prevalence of radiographic abnormalities among Northern California shipyard workers
-
Polakoff PL, Horn BR, Scherer OR. Prevalence of radiographic abnormalities among Northern California shipyard workers. Ann N Y Acad Sci. 1979;330:333-339.
-
(1979)
Ann N y Acad Sci.
, vol.330
, pp. 333-339
-
-
Polakoff, P.L.1
Horn, B.R.2
Scherer, O.R.3
-
13
-
-
7844226301
-
Expression of TNF and the necessity of TNF receptors in bleomycin-induced lung injury in mice
-
Ortiz LA, Lasky J, Hamilton RF Jr, et al. Expression of TNF and the necessity of TNF receptors in bleomycin-induced lung injury in mice. Exp Lung Res. 1998;24:721-743.
-
(1998)
Exp Lung Res.
, vol.24
, pp. 721-743
-
-
Ortiz, L.A.1
Lasky, J.2
Hamilton Jr., R.F.3
-
14
-
-
0036891072
-
Susceptibility to asbestos-induced and transforming growth factor-beta1-induced fibroproliferative lung disease in two strains of mice
-
Warshamana GS, Pociask DA, Sime P, et al. Susceptibility to asbestos-induced and transforming growth factor-beta1-induced fibroproliferative lung disease in two strains of mice. Am J Respir Cell Mol Biol. 2002;27:705-713.
-
(2002)
Am J Respir Cell Mol Biol.
, vol.27
, pp. 705-713
-
-
Warshamana, G.S.1
Pociask, D.A.2
Sime, P.3
-
15
-
-
0018974998
-
Idiopathic pulmonary fibrosis in monozygotic twins. The importance of genetic predisposition
-
Javaheri S, Lederer DH, Pella JA, et al. Idiopathic pulmonary fibrosis in monozygotic twins. The importance of genetic predisposition. Chest. 1980;78:591-594.
-
(1980)
Chest.
, vol.78
, pp. 591-594
-
-
Javaheri, S.1
Lederer, D.H.2
Pella, J.A.3
-
16
-
-
0000959869
-
A family study of idiopathic pulmonary fibrosis. A possible dysproteinemic and genetically determined disease
-
Bonanni PP, Frymoyer JW, Jacox RF. A family study of idiopathic pulmonary fibrosis. A possible dysproteinemic and genetically determined disease. Am J Med. 1965;39:411-421.
-
(1965)
Am J Med.
, vol.39
, pp. 411-421
-
-
Bonanni, P.P.1
Frymoyer, J.W.2
Jacox, R.F.3
-
18
-
-
30344471883
-
Clinical and pathologic features of familial interstitial pneumonia
-
Steele MP, Speer MC, Loyd JE, et al. Clinical and pathologic features of familial interstitial pneumonia. Am J Respir Crit Care Med. 2005;172:1146-1152.
-
(2005)
Am J Respir Crit Care Med.
, vol.172
, pp. 1146-1152
-
-
Steele, M.P.1
Speer, M.C.2
Loyd, J.E.3
-
20
-
-
0020894981
-
Interstitial pulmonary fibrosis in two sisters. Possible autosomal recessive inheritance
-
Tsukahara M, Kajii T. Interstitial pulmonary fibrosis in two sisters. Possible autosomal recessive inheritance. Jinrui Idengaku Zasshi. 1983;28:263-267.
-
(1983)
Jinrui Idengaku Zasshi.
, vol.28
, pp. 263-267
-
-
Tsukahara, M.1
Kajii, T.2
-
21
-
-
21844478279
-
Familial idiopathic pulmonary fibrosis: Clinical features and outcome
-
Lee HL, Ryu JH, Wittmer MH, et al. Familial idiopathic pulmonary fibrosis: clinical features and outcome. Chest. 2005;127:2034-2041.
-
(2005)
Chest.
, vol.127
, pp. 2034-2041
-
-
Lee, H.L.1
Ryu, J.H.2
Wittmer, M.H.3
-
22
-
-
0034018105
-
Adult familial cryptogenic fibrosing alveolitis in the United Kingdom
-
Marshall RP, Puddicombe A, Cookson WO, et al. Adult familial cryptogenic fibrosing alveolitis in the United Kingdom. Thorax. 2000;55:143-146.
-
(2000)
Thorax.
, vol.55
, pp. 143-146
-
-
Marshall, R.P.1
Puddicombe, A.2
Cookson, W.O.3
-
23
-
-
79955146233
-
A common MUC5B promoter polymorphism and pulmonary fibrosis
-
Seibold MA, Wise AL, Speer MC, et al. A common MUC5B promoter polymorphism and pulmonary fibrosis. N Engl J Med. 2011;364:1503-1512.
-
(2011)
N Engl J Med.
, vol.364
, pp. 1503-1512
-
-
Seibold, M.A.1
Wise, A.L.2
Speer, M.C.3
-
24
-
-
0036214069
-
Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: Evidence of founder effect among multiplex families in Finland
-
Hodgson U, Laitinen T, Tukiainen P. Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: evidence of founder effect among multiplex families in Finland. Thorax. 2002;57:338-342.
-
(2002)
Thorax.
, vol.57
, pp. 338-342
-
-
Hodgson, U.1
Laitinen, T.2
Tukiainen, P.3
-
26
-
-
78649859428
-
Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort
-
van Moorsel CH, van Oosterhout MF, Barlo NP, et al. Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort. Am J Respir Crit Care Med. 2010;182:1419-1425.
-
(2010)
Am J Respir Crit Care Med.
, vol.182
, pp. 1419-1425
-
-
Van Moorsel, C.H.1
Van Oosterhout, M.F.2
Barlo, N.P.3
-
27
-
-
81155152241
-
Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis
-
Garcia-Sancho C, Buendia-Roldan I, Fernandez-Plata MR, et al. Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis. Respir Med. 2011;105: 1902-1907.
-
(2011)
Respir Med.
, vol.105
, pp. 1902-1907
-
-
Garcia-Sancho, C.1
Buendia-Roldan, I.2
Fernandez-Plata, M.R.3
-
29
-
-
36849039441
-
Diffuse lung disease in young children: Application of a novel classification scheme
-
Deutsch GH, Young LR, Deterding RR, et al. Diffuse lung disease in young children: application of a novel classification scheme. Am J Respir Crit Care Med. 2007;176:1120-1128.
-
(2007)
Am J Respir Crit Care Med.
, vol.176
, pp. 1120-1128
-
-
Deutsch, G.H.1
Young, L.R.2
Deterding, R.R.3
-
30
-
-
34250643070
-
Genetic disorders of surfactant proteins
-
Hamvas A, Cole FS, Nogee LM. Genetic disorders of surfactant proteins. Neonatology. 2007;91:311-317.
-
(2007)
Neonatology.
, vol.91
, pp. 311-317
-
-
Hamvas, A.1
Cole, F.S.2
Nogee, L.M.3
-
31
-
-
77951909085
-
Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease
-
Whitsett JA, Wert SE, Weaver TE. Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease. Annu Rev Med. 2010;61:105-119.
-
(2010)
Annu Rev Med.
, vol.61
, pp. 105-119
-
-
Whitsett, J.A.1
Wert, S.E.2
Weaver, T.E.3
-
32
-
-
34547617163
-
Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation
-
Bullard JE, Nogee LM. Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation. Pediatr Res. 2007;62: 176-179.
-
(2007)
Pediatr Res.
, vol.62
, pp. 176-179
-
-
Bullard, J.E.1
Nogee, L.M.2
-
33
-
-
0035931973
-
A mutation in the surfactant protein C gene associated with familial interstitial lung disease
-
Nogee LM, Dunbar AE III, Wert SE, et al. A mutation in the surfactant protein C gene associated with familial interstitial lung disease. N Engl J Med. 2001;344:573-579.
-
(2001)
N Engl J Med.
, vol.344
, pp. 573-579
-
-
Nogee, L.M.1
Dunbar Iii., A.E.2
Wert, S.E.3
-
34
-
-
0036570052
-
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
-
Thomas AQ, Lane K, Phillips J III, et al. Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred. Am J Respir Crit Care Med. 2002;165:1322-1328.
-
(2002)
Am J Respir Crit Care Med.
, vol.165
, pp. 1322-1328
-
-
Thomas, A.Q.1
Lane, K.2
Phillips Iii., J.3
-
35
-
-
84864406003
-
A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: Clinical and genetic features
-
Fernandez BA, Fox G, Bhatia R, et al. A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features. Respir Res. 2012;64:1-10.
-
(2012)
Respir Res.
, vol.64
, pp. 1-10
-
-
Fernandez, B.A.1
Fox, G.2
Bhatia, R.3
-
36
-
-
33846236874
-
Surfactant protein C mutations in sporadic forms of idiopathic interstitial pneumonias
-
Markart P, Ruppert C, Wygrecka M, et al. Surfactant protein C mutations in sporadic forms of idiopathic interstitial pneumonias. Eur Respir J. 2007;29:134-137.
-
(2007)
Eur Respir J.
, vol.29
, pp. 134-137
-
-
Markart, P.1
Ruppert, C.2
Wygrecka, M.3
-
37
-
-
8544245673
-
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
-
Lawson WE, Grant SW, Ambrosini V, et al. Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF. Thorax. 2004;59:977-980.
-
(2004)
Thorax.
, vol.59
, pp. 977-980
-
-
Lawson, W.E.1
Grant, S.W.2
Ambrosini, V.3
-
38
-
-
58149159548
-
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer
-
Wang Y, Kuan PJ, Xing C, et al. Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet. 2009;84:52-59.
-
(2009)
Am J Hum Genet.
, vol.84
, pp. 52-59
-
-
Wang, Y.1
Kuan, P.J.2
Xing, C.3
-
40
-
-
67650079362
-
Syndromes of telomere shortening
-
Armanios M. Syndromes of telomere shortening. Annu Rev Genomics Hum Genet. 2009;10:45-61.
-
(2009)
Annu Rev Genomics Hum Genet.
, vol.10
, pp. 45-61
-
-
Armanios, M.1
-
42
-
-
38049019132
-
Human diseases of telomerase dysfunction: Insights into tissue aging
-
Garcia CK, Wright WE, Shay JW. Human diseases of telomerase dysfunction: insights into tissue aging. Nucleic Acids Res. 2007;35:7406-7416.
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 7406-7416
-
-
Garcia, C.K.1
Wright, W.E.2
Shay, J.W.3
-
43
-
-
51349113450
-
Short telomeres are a risk factor for idiopathic pulmonary fibrosis
-
Alder JK, Chen JJ, Lancaster L, et al. Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proc Natl Acad Sci USA. 2008;105:13051-13056.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 13051-13056
-
-
Alder, J.K.1
Chen, J.J.2
Lancaster, L.3
-
44
-
-
34047188508
-
Telomerase mutations in families with idiopathic pulmonary fibrosis
-
Armanios MY, Chen JJ, Cogan JD, et al. Telomerase mutations in families with idiopathic pulmonary fibrosis. N Engl J Med. 2007;356:1317-1326.
-
(2007)
N Engl J Med.
, vol.356
, pp. 1317-1326
-
-
Armanios, M.Y.1
Chen, J.J.2
Cogan, J.D.3
-
45
-
-
34250614359
-
Adult-onset pulmonary fibrosis caused by mutations in telomerase
-
Tsakiri KD, Cronkhite JT, Kuan PJ, et al. Adult-onset pulmonary fibrosis caused by mutations in telomerase. Proc Natl Acad Sci USA. 2007;104:7552-7557.
-
(2007)
Proc Natl Acad Sci USA.
, vol.104
, pp. 7552-7557
-
-
Tsakiri, K.D.1
Cronkhite, J.T.2
Kuan, P.J.3
-
46
-
-
77956289135
-
Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations
-
Diaz de Leon A, Cronkhite JT, Katzenstein AL, et al. Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations. PLoS One. 2010;5:e10680.
-
(2010)
PLoS One.
, vol.5
-
-
Diaz De Leon, A.1
Cronkhite, J.T.2
Katzenstein, A.L.3
-
47
-
-
52749083873
-
Telomere shortening in familial and sporadic pulmonary fibrosis
-
Cronkhite JT, Xing C, Raghu G, et al. Telomere shortening in familial and sporadic pulmonary fibrosis. Am J Respir Crit Care Med. 2008;178:729-737.
-
(2008)
Am J Respir Crit Care Med.
, vol.178
, pp. 729-737
-
-
Cronkhite, J.T.1
Xing, C.2
Raghu, G.3
-
48
-
-
84878686854
-
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
-
Fingerlin TE, Murphy E, Zhang W, et al. Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. Nat Genet. 2013;45:613-620.
-
(2013)
Nat Genet.
, vol.45
, pp. 613-620
-
-
Fingerlin, T.E.1
Murphy, E.2
Zhang, W.3
-
49
-
-
0037157582
-
Association between aplastic anaemia and mutations in telomerase RNA
-
Vulliamy T, Marrone A, Dokal I, et al. Association between aplastic anaemia and mutations in telomerase RNA. Lancet. 2002;359:2168-2170.
-
(2002)
Lancet.
, vol.359
, pp. 2168-2170
-
-
Vulliamy, T.1
Marrone, A.2
Dokal, I.3
-
50
-
-
15944422499
-
Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia
-
Yamaguchi H, Calado RT, Ly H, et al. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. N Engl J Med. 2005;352:1413-1424.
-
(2005)
N Engl J Med.
, vol.352
, pp. 1413-1424
-
-
Yamaguchi, H.1
Calado, R.T.2
Ly, H.3
-
51
-
-
0041592752
-
Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
-
Yamaguchi H, Baerlocher GM, Lansdorp PM, et al. Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. Blood. 2003;102:916-918.
-
(2003)
Blood.
, vol.102
, pp. 916-918
-
-
Yamaguchi, H.1
Baerlocher, G.M.2
Lansdorp, P.M.3
-
52
-
-
79955119666
-
Constitutional telomerase mutations are genetic risk factors for cirrhosis
-
Calado RT, Brudno J, Mehta P, et al. Constitutional telomerase mutations are genetic risk factors for cirrhosis. Hepatology. 2011;53:1600-1607.
-
(2011)
Hepatology.
, vol.53
, pp. 1600-1607
-
-
Calado, R.T.1
Brudno, J.2
Mehta, P.3
-
53
-
-
84855473741
-
Telomerase and idiopathic pulmonary fibrosis
-
Armanios M. Telomerase and idiopathic pulmonary fibrosis. Mut Res. 2012;730:52-58.
-
(2012)
Mut Res.
, vol.730
, pp. 52-58
-
-
Armanios, M.1
-
54
-
-
33745282150
-
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
-
Hodgson U, Pulkkinen V, Dixon M, et al. ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis. Am J Hum Genet. 2006;79:149-154.
-
(2006)
Am J Hum Genet.
, vol.79
, pp. 149-154
-
-
Hodgson, U.1
Pulkkinen, V.2
Dixon, M.3
-
55
-
-
77951645406
-
ELMOD2, a candidate gene for idiopathic pulmonary fibrosis, regulates antiviral responses
-
Pulkkinen V, Bruce S, Rintahaka J, et al. ELMOD2, a candidate gene for idiopathic pulmonary fibrosis, regulates antiviral responses. FASEB J. 2010;24:1167-1177.
-
(2010)
FASEB J.
, vol.24
, pp. 1167-1177
-
-
Pulkkinen, V.1
Bruce, S.2
Rintahaka, J.3
-
56
-
-
79955144623
-
A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis
-
Zhang Y, Noth I, Garcia JG, et al. A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis. N Engl J Med. 2011;364:1576-1577.
-
(2011)
N Engl J Med.
, vol.364
, pp. 1576-1577
-
-
Zhang, Y.1
Noth, I.2
Garcia, J.G.3
-
57
-
-
84880043679
-
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: A genome-wide association study
-
Noth Iea.
-
Noth Iea. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. Lancet Respir Med. 2013;1:309-317.
-
(2013)
Lancet Respir Med.
, vol.1
, pp. 309-317
-
-
-
58
-
-
84878600828
-
Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
-
Peljto AL, Zhang Y, Fingerlin TE, et al. Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis. JAMA. 2013;1-8.
-
(2013)
JAMA.
, pp. 1-8
-
-
Peljto, A.L.1
Zhang, Y.2
Fingerlin, T.E.3
-
59
-
-
54049136464
-
A genomewide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis
-
Mushiroda T, Wattanapokayakit S, Takahashi A, et al. A genomewide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. J Med Genet. 2008;45: 654-656.
-
(2008)
J Med Genet.
, vol.45
, pp. 654-656
-
-
Mushiroda, T.1
Wattanapokayakit, S.2
Takahashi, A.3
-
60
-
-
84899825224
-
-
Genetic Information Nondiscrimination Act of 2008, Public Law 110-233, 42 USC, 122 STAT 181, 2008.
-
Genetic Information Nondiscrimination Act of 2008, Public Law 110-233, 42 USC, 122 STAT 181, 2008
-
-
-
|