-
1
-
-
13144296251
-
-
Tri-Council. Canada: Public Works and Government Services
-
Tri-Council. Ethical conduct for research involving humans. Canada: Public Works and Government Services, 2003.
-
(2003)
Ethical Conduct for Research Involving Humans
-
-
-
2
-
-
85205867397
-
-
World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects
-
World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects, 1964.
-
(1964)
-
-
-
3
-
-
70349150731
-
The Belmont Report: Ethical principles and guidelines for the protection of human subjects of research
-
The Belmont Report: ethical principles and guidelines for the protection of human subjects of research. US Department of Health Education, and Welfare, 1979.
-
(1979)
US Department of Health Education, and Welfare
-
-
-
4
-
-
12344329691
-
Permission to publish case reports/case series
-
Bevan JC, Hardy JF. Permission to publish case reports/case series. Can J Anaesth 2004;51:861-866.
-
(2004)
Can J Anaesth
, vol.51
, pp. 861-866
-
-
Bevan, J.C.1
Hardy, J.F.2
-
5
-
-
1642364627
-
The ethics of case reports
-
Shevell M. The ethics of case reports. Paediatr Child Health 2004;9:83-84.
-
(2004)
Paediatr Child Health
, vol.9
, pp. 83-84
-
-
Shevell, M.1
-
6
-
-
33644795291
-
Genetic knowledge and moral responsibility: Ambiguity at the interface of genetic research and clinical practice
-
Pullman D, Hodgkinson K. Genetic knowledge and moral responsibility: ambiguity at the interface of genetic research and clinical practice. Clin Genet 2006;69:199-203.
-
(2006)
Clin Genet
, vol.69
, pp. 199-203
-
-
Pullman, D.1
Hodgkinson, K.2
-
7
-
-
3142699826
-
Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation
-
Abkevich V, Zharkikh A, Deffenbaugh AM, Frank D, et al. Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation. J Med Genet 2004;41:492-507.
-
(2004)
J Med Genet
, vol.41
, pp. 492-507
-
-
Abkevich, V.1
Zharkikh, A.2
Deffenbaugh, A.M.3
Frank, D.4
-
8
-
-
13444292150
-
Classification of BRCA1 missense variants of unknown clinical significance
-
Phelan CM, Dapic V, Tice B, Favis R, et al. Classification of BRCA1 missense variants of unknown clinical significance. J Med Genet 2005;42:138-146.
-
(2005)
J Med Genet
, vol.42
, pp. 138-146
-
-
Phelan, C.M.1
Dapic, V.2
Tice, B.3
Favis, R.4
-
9
-
-
33744506819
-
Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype
-
Piovani G, Borsani G, Bertini V, Kalscheuer VM, et al. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype. Eur J Med Genet 2006;49:215-223.
-
(2006)
Eur J Med Genet
, vol.49
, pp. 215-223
-
-
Piovani, G.1
Borsani, G.2
Bertini, V.3
Kalscheuer, V.M.4
-
10
-
-
4444312172
-
A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irises
-
Spruijt L, Engelen JJ, Bruinen-Smeijsters IP, Albrechts JC, et al. A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irises. Am J Med Genet A 2004;129:312-315.
-
(2004)
Am J Med Genet A
, vol.129
, pp. 312-315
-
-
Spruijt, L.1
Engelen, J.J.2
Bruinen-Smeijsters, I.P.3
Albrechts, J.C.4
-
11
-
-
25644446165
-
Detection of an unexpected subtelomeric 15q26.2 3qter deletion in a little girl: Clinical and cytogenetic studies
-
Pinson L, Perrin A, Plouzennec C, Parent P, et al. Detection of an unexpected subtelomeric 15q26.2 3qter deletion in a little girl: clinical and cytogenetic studies. Am J Med Genet A 2005;138:160-165.
-
(2005)
Am J Med Genet A
, vol.138
, pp. 160-165
-
-
Pinson, L.1
Perrin, A.2
Plouzennec, C.3
Parent, P.4
-
12
-
-
33748202535
-
A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions
-
Baynam G, Goldblatt J, Townshend S. A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions. Clin Dysmor-phol 2006;15:145-148.
-
(2006)
Clin Dysmor-phol
, vol.15
, pp. 145-148
-
-
Baynam, G.1
Goldblatt, J.2
Townshend, S.3
-
13
-
-
33749465589
-
Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation
-
Rauch A, Hoyer J, Guth S, Zweier C, et al. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. Am J Med Genet A 2006;140:2063-2074.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 2063-2074
-
-
Rauch, A.1
Hoyer, J.2
Guth, S.3
Zweier, C.4
-
14
-
-
34548650911
-
Congenital myopathy with nema-line rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)
-
Tajsharghi H, Ohlsson M, Lindberg C, Oldfors A. Congenital myopathy with nema-line rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2). Arch Neurol 2007;64:1334-1338.
-
(2007)
Arch Neurol
, vol.64
, pp. 1334-1338
-
-
Tajsharghi, H.1
Ohlsson, M.2
Lindberg, C.3
Oldfors, A.4
-
15
-
-
34648823742
-
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene
-
Al-Dirbashi OY, Abu-Amero KK, Alswaid AF, Hoffmann GF, et al. LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene. J Inherit Metab Dis 2007;30:611.
-
(2007)
J Inherit Metab Dis
, vol.30
, pp. 611
-
-
Al-Dirbashi, O.Y.1
Abu-Amero, K.K.2
Alswaid, A.F.3
Hoffmann, G.F.4
-
16
-
-
34249009175
-
A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis
-
Shrimpton AE, Schelper RL, Linke RP, Hardy J, et al. A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis. Neuropathology 2007;27:228-232.
-
(2007)
Neuropathology
, vol.27
, pp. 228-232
-
-
Shrimpton, A.E.1
Schelper, R.L.2
Linke, R.P.3
Hardy, J.4
-
17
-
-
34247510232
-
Subtelomeric deletion 9qter: Definition of the syndrome and parental origin in 2 patients
-
Rosello M, Monfort S, Orellana C, Oltra S, et al. [Subtelomeric deletion 9qter: definition of the syndrome and parental origin in 2 patients]. Med Clin (Barc) 2007;128:419-421.
-
(2007)
Med Clin (Barc)
, vol.128
, pp. 419-421
-
-
Rosello, M.1
Monfort, S.2
Orellana, C.3
Oltra, S.4
-
18
-
-
34250624022
-
Localized autosomal recessive hypotricho-sis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family
-
Wajid M, Bazzi H, Rockey J, Lubetkin J, et al. Localized autosomal recessive hypotricho-sis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family. J Invest Dermatol 2007;127:1779-1782.
-
(2007)
J Invest Dermatol
, vol.127
, pp. 1779-1782
-
-
Wajid, M.1
Bazzi, H.2
Rockey, J.3
Lubetkin, J.4
-
19
-
-
4043108399
-
Ethical review of research into rare genetic disorders
-
Parker M, Ashcroft R, Wilkie AO, Kent A. Ethical review of research into rare genetic disorders. BMJ 2004;31 329:288-289.
-
(2004)
BMJ
, vol.31
, Issue.329
, pp. 288-289
-
-
Parker, M.1
Ashcroft, R.2
Wilkie, A.O.3
Kent, A.4
-
20
-
-
0031790040
-
Use of isolated inbred human populations for identification of disease genes
-
Sheffield VC, Stone EM, Carmi R. Use of isolated inbred human populations for identification of disease genes. Trends Genet 1998;14:391-396.
-
(1998)
Trends Genet
, vol.14
, pp. 391-396
-
-
Sheffield, V.C.1
Stone, E.M.2
Carmi, R.3
-
21
-
-
25144485002
-
Population history and its impact on medical genetics in Quebec
-
Laberge AM, Michaud J, Richter A, Lemyre E, et al. Population history and its impact on medical genetics in Quebec. Clin Genet 2005;68:287-301.
-
(2005)
Clin Genet
, vol.68
, pp. 287-301
-
-
Laberge, A.M.1
Michaud, J.2
Richter, A.3
Lemyre, E.4
-
22
-
-
0032869123
-
Molecular genetics of the Finnish disease heritage
-
Peltonen L, Jalanko A, Varilo T. Molecular genetics of the Finnish disease heritage. Hum Mol Genet 1999;8:1913-1923.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1913-1923
-
-
Peltonen, L.1
Jalanko, A.2
Varilo, T.3
-
23
-
-
19944433030
-
The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)
-
Hodgkinson KA, Parfrey PS, Bassett AS, Kupprion C, et al. The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5). J Am Coll Cardiol 2005;45:400-408.
-
(2005)
J Am Coll Cardiol
, vol.45
, pp. 400-408
-
-
Hodgkinson, K.A.1
Parfrey, P.S.2
Bassett, A.S.3
Kupprion, C.4
-
24
-
-
2442670243
-
Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia
-
Leren TP. Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia. Clin Genet 2004;65:419-422.
-
(2004)
Clin Genet
, vol.65
, pp. 419-422
-
-
Leren, T.P.1
-
25
-
-
12144285659
-
A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree
-
Timms KM, Wagner S, Samuels ME, et al. A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree. Hum Genet 2004;114:349-353.
-
(2004)
Hum Genet
, vol.114
, pp. 349-353
-
-
Timms, K.M.1
Wagner, S.2
Samuels, M.E.3
-
26
-
-
33947389328
-
Mutation hotspots of SCN9A in primary erythermalgia
-
Zhang LL, Lin ZM, Ma ZH, Xu Z, et al. Mutation hotspots of SCN9A in primary erythermalgia. Br J Dermatol 2007;156:767-769.
-
(2007)
Br J Dermatol
, vol.156
, pp. 767-769
-
-
Zhang, L.L.1
Lin, Z.M.2
Ma, Z.H.3
Xu, Z.4
-
27
-
-
34249323364
-
Linkage mapping
-
Canada: John Wiley & Sons
-
Samuels ME, Dube MP. Linkage mapping. In: Encyclopedia of genetics, genomics, proteomics, and bioinformatics, part 2, Genetics, Canada: John Wiley & Sons, 2005.
-
(2005)
Encyclopedia of Genetics, Genomics, Proteomics, and Bioinformatics, Part 2, Genetics
-
-
Samuels, M.E.1
Dube, M.P.2
-
28
-
-
34249314767
-
New technologies in human genetic analysis
-
Samuels M, Higgins B, Provost S, Marcadier J, et al. New technologies in human genetic analysis. Am Biotechnol Lab 2007;25:22-27.
-
(2007)
Am Biotechnol Lab
, vol.25
, pp. 22-27
-
-
Samuels, M.1
Higgins, B.2
Provost, S.3
Marcadier, J.4
-
29
-
-
12144286180
-
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array
-
Matsuzaki H, Loi H, Dong S, Tsai YY, et al. Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array. Genome Res 2004; 14:414-425.
-
(2004)
Genome Res
, vol.14
, pp. 414-425
-
-
Matsuzaki, H.1
Loi, H.2
Dong, S.3
Tsai, Y.Y.4
-
30
-
-
15444364646
-
Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays
-
Sellick GS, Longman C, Tolmie J, Newbury-Ecob R, et al. Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays. Nucl Acids Res 2004;32:e164.
-
(2004)
Nucl Acids Res
, vol.32
-
-
Sellick, G.S.1
Longman, C.2
Tolmie, J.3
Newbury-Ecob, R.4
-
31
-
-
33746363353
-
Structural variants: Changing the landscape of chromosomes and design of disease studies
-
Feuk L, Marshall CR, Wintle RF, Scherer SW. Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Genet 2006;15 Spec No 1:R57-R66.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.SPEC. 1
-
-
Feuk, L.1
Marshall, C.R.2
Wintle, R.F.3
Scherer, S.W.4
-
32
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon R, Ishikawa S, Fitch KR, Feuk L, et al. Global variation in copy number in the human genome. Nature 2006;444:444-454. (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
33
-
-
33748644928
-
Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation
-
Friedman JM, Baross A, Delaney AD, Ally A, et al. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation. Am J Hum Genet 2006;79:500-513.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 500-513
-
-
Friedman, J.M.1
Baross, A.2
Delaney, A.D.3
Ally, A.4
-
34
-
-
34548677263
-
Array-based comparative genomic hybridization: Clinical contexts for targeted and whole-genome designs
-
Aradhya S, Cherry AM. Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs. Genet Med 2007;9:553-559.
-
(2007)
Genet Med
, vol.9
, pp. 553-559
-
-
Aradhya, S.1
Cherry, A.M.2
-
35
-
-
34548670712
-
Use of array-based technology in the practice of medical genetics
-
Manning M, Hudgins L. Use of array-based technology in the practice of medical genetics. Genet Med 2007;9:650-653.
-
(2007)
Genet Med
, vol.9
, pp. 650-653
-
-
Manning, M.1
Hudgins, L.2
-
36
-
-
37648999313
-
Distinguishing protein-coding and noncod-ing genes in the human genome
-
Clamp M, Fry B, Kamal M, Xie X, et al. Distinguishing protein-coding and noncod-ing genes in the human genome. Proc Natl Acad Sci USA 2007;104:19428-19433.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 19428-19433
-
-
Clamp, M.1
Fry, B.2
Kamal, M.3
Xie, X.4
-
37
-
-
33645130154
-
Mendelian disorders deserve more attention
-
Antonarakis SE, Beckmann JS. Mendelian disorders deserve more attention. Nat Rev Genet 2006;7:277-282.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 277-282
-
-
Antonarakis, S.E.1
Beckmann, J.S.2
-
38
-
-
79959503826
-
The International HapMap Project
-
The International HapMap Project. Nature 2003;426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
39
-
-
34547817696
-
New perspectives for the elucidation of genetic disorders
-
Ropers HH. New perspectives for the elucidation of genetic disorders. Am J Hum Genet 2007;81:199-207.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 199-207
-
-
Ropers, H.H.1
-
40
-
-
34548675362
-
Ethical implications of array comparative genomic hybridization in complex phenotypes: Points to consider in research
-
Tabor HK, Cho MK. Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research. Genet Med 2007;9:626-631.
-
(2007)
Genet Med
, vol.9
, pp. 626-631
-
-
Tabor, H.K.1
Cho, M.K.2
-
41
-
-
33749454767
-
The post-human genome project mindset: Race, reliability, and health care
-
Kimmelman J. The post-human genome project mindset: race, reliability, and health care. Clin Genet 2006;70:427-432.
-
(2006)
Clin Genet
, vol.70
, pp. 427-432
-
-
Kimmelman, J.1
-
42
-
-
8244257360
-
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations
-
Kerem E, Rave-Harel N, Augarten A, Madgar I, et al. A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations. Am J Respir Crit Care Med 1997;155:1914-1920.
-
(1997)
Am J Respir Crit Care Med
, vol.155
, pp. 1914-1920
-
-
Kerem, E.1
Rave-Harel, N.2
Augarten, A.3
Madgar, I.4
-
43
-
-
33644931158
-
Cystic fibrosis mutations with widely variable phenotype: The D1152H example
-
Mussaffi H, Prais D, Mei-Zahav M, Blau H. Cystic fibrosis mutations with widely variable phenotype: the D1152H example. Pediatr Pulmonol 2006;41:250-254.
-
(2006)
Pediatr Pulmonol
, vol.41
, pp. 250-254
-
-
Mussaffi, H.1
Prais, D.2
Mei-Zahav, M.3
Blau, H.4
-
44
-
-
0033168957
-
Monogenic traits are not simple: Lessons from phenylketo-nuria
-
Scriver CR, Waters PJ. Monogenic traits are not simple: lessons from phenylketo-nuria. Trends Genet 1999;15:267-272.
-
(1999)
Trends Genet
, vol.15
, pp. 267-272
-
-
Scriver, C.R.1
Waters, P.J.2
-
45
-
-
33846082765
-
Newborn screening: Toward a uniform screening panel and system-executive summary
-
Watson MS, Mann MY, Lloyd-Puryear M, Rinaldo P, et al. Newborn screening: toward a uniform screening panel and system-executive summary. Pediatrics 2006;117(5 pt 2):S296-S307.
-
(2006)
Pediatrics
, vol.117
, Issue.5 PART 2
-
-
Watson, M.S.1
Mann, M.Y.2
Lloyd-Puryear, M.3
Rinaldo, P.4
-
46
-
-
33744832631
-
Economic evaluation of tandem mass spectrometry screening in California
-
Feuchtbaum L, Cunningham G. Economic evaluation of tandem mass spectrometry screening in California. Pediatrics 2006;117(5 pt 2):S280-S286.
-
(2006)
Pediatrics
, vol.117
, Issue.5 PART 2
-
-
Feuchtbaum, L.1
Cunningham, G.2
-
47
-
-
0036791226
-
Cost-benefit analysis of universal tandem mass spectrometry for newborn screening
-
Schoen EJ, Baker JC, Colby CJ, To TT. Cost-benefit analysis of universal tandem mass spectrometry for newborn screening. Pediatrics 2002;110:781-786.
-
(2002)
Pediatrics
, vol.110
, pp. 781-786
-
-
Schoen, E.J.1
Baker, J.C.2
Colby, C.J.3
To, T.T.4
-
48
-
-
0029814661
-
Cost comparison of molecular versus conventional screening of relatives at risk for retinoblastoma
-
Noorani HZ, Khan HN, Gallie BL, Detsky AS. Cost comparison of molecular versus conventional screening of relatives at risk for retinoblastoma. Am J Hum Genet 1996;59:301-307.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 301-307
-
-
Noorani, H.Z.1
Khan, H.N.2
Gallie, B.L.3
Detsky, A.S.4
-
50
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy S, Sutton G, Ng PC, Feuk L, et al. The diploid genome sequence of an individual human. PLoS Biol 2007;5:e2000000000054.
-
(2007)
PLoS Biol
, vol.5
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
Feuk, L.4
-
51
-
-
42249087308
-
The complete genome of an individual by massively parallel DNA sequencing
-
Wheeler DA, Srinivasan M, Egholm M, Shen Y, et al. The complete genome of an individual by massively parallel DNA sequencing. Nature 2008;452:872-876.
-
(2008)
Nature
, vol.452
, pp. 872-876
-
-
Wheeler, D.A.1
Srinivasan, M.2
Egholm, M.3
Shen, Y.4
-
52
-
-
85205847901
-
The impact of new DNA sequencing technologies on human genetics
-
Montreal
-
Bentley D. The impact of new DNA sequencing technologies on human genetics. HUGO HGM2007. Montreal, 2007.
-
(2007)
HUGO HGM2007
-
-
Bentley, D.1
-
53
-
-
33750953227
-
Whole-genome re-sequencing
-
Bentley DR. Whole-genome re-sequencing. Curr Opin Genet Dev 2006;16:545-552.
-
(2006)
Curr Opin Genet Dev
, vol.16
, pp. 545-552
-
-
Bentley, D.R.1
-
54
-
-
33845212250
-
Anticipating the 1,000 dollar genome
-
Mardis ER. Anticipating the 1,000 dollar genome. Genome Biol 2006;7:112.
-
(2006)
Genome Biol
, vol.7
, pp. 112
-
-
Mardis, E.R.1
-
55
-
-
85012480728
-
The $1000 genome: Ethical and legal issues in whole genome sequencing of individuals
-
Robertson JA. The $1000 genome: ethical and legal issues in whole genome sequencing of individuals. Am J Bioeth 2003;3:W-IF1.
-
(2003)
Am J Bioeth
, vol.3
-
-
Robertson, J.A.1
-
56
-
-
38549085235
-
Research ethics and the challenge of whole-genome sequencing
-
McGuire AL, Caulfield T, Cho MK. Research ethics and the challenge of whole-genome sequencing. Nat Rev Genet 2008;9:152-156.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 152-156
-
-
McGuire, A.L.1
Caulfield, T.2
Cho, M.K.3
-
57
-
-
1642463352
-
Ethics review roulette: What can we learn
-
Glasziou P, Chalmers I. Ethics review roulette: what can we learn? BMJ 2004;328: 121-122.
-
(2004)
BMJ
, vol.328
, pp. 121-122
-
-
Glasziou, P.1
Chalmers, I.2
-
58
-
-
0034795716
-
Ethical approval for research involving geographically dispersed subjects: Unsuitability of the UK MREC/LREC system and relevance to uncommon genetic disorders
-
Lewis JC, Tomkins S, Sampson JR. Ethical approval for research involving geographically dispersed subjects: unsuitability of the UK MREC/LREC system and relevance to uncommon genetic disorders. J Med Ethics 2001;27:347-351.
-
(2001)
J Med Ethics
, vol.27
, pp. 347-351
-
-
Lewis, J.C.1
Tomkins, S.2
Sampson, J.R.3
-
59
-
-
16844380496
-
Cost-effectiveness and evidence evaluation as criteria for coverage policy
-
Web Exclusives
-
Garber AM. Cost-effectiveness and evidence evaluation as criteria for coverage policy. Health Aff (Millwood) 2004;Suppl Web Exclusives: W4-284-296.
-
(2004)
Health Aff (Millwood)
, Issue.SUPPL.
-
-
Garber, A.M.1
-
60
-
-
85205880218
-
Mapping fate.
-
Wexler A. Mapping fate. Crown, 1995.
-
(1995)
Crown
-
-
Wexler, A.1
-
61
-
-
33746924446
-
Gene tests: An online genetic information resource for health care providers
-
Pagon RA. Gene tests: an online genetic information resource for health care providers. J Med Libr Assoc 2006;94:343-348.
-
(2006)
J Med Libr Assoc
, vol.94
, pp. 343-348
-
-
Pagon, R.A.1
|