-
1
-
-
84863393160
-
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
-
S1-S2, 10.1038/ng.1083, 3428915, 22366785
-
Albers CA, Paul DS, Schulze H, Freson K, Stephens JC, Smethurst PA, Jolley JD, Cvejic A, Kostadima M, Bertone P, Breuning MH, Debili N, Deloukas P, Favier R, Fiedler J, Hobbs CM, Huang N, Hurles ME, Kiddle G, Krapels I, Nurden P, Ruivenkamp CA, Sambrook JG, Smith K, Stemple DL, Strauss G, Thys C, van Geet C, Newbury-Ecob R, Ouwehand WH, Ghevaert C. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet 2012, 44:435-9. S1-S2, 10.1038/ng.1083, 3428915, 22366785.
-
(2012)
Nat Genet
, vol.44
, pp. 435-439
-
-
Albers, C.A.1
Paul, D.S.2
Schulze, H.3
Freson, K.4
Stephens, J.C.5
Smethurst, P.A.6
Jolley, J.D.7
Cvejic, A.8
Kostadima, M.9
Bertone, P.10
Breuning, M.H.11
Debili, N.12
Deloukas, P.13
Favier, R.14
Fiedler, J.15
Hobbs, C.M.16
Huang, N.17
Hurles, M.E.18
Kiddle, G.19
Krapels, I.20
Nurden, P.21
Ruivenkamp, C.A.22
Sambrook, J.G.23
Smith, K.24
Stemple, D.L.25
Strauss, G.26
Thys, C.27
van Geet, C.28
Newbury-Ecob, R.29
Ouwehand, W.H.30
Ghevaert, C.31
more..
-
2
-
-
84870516109
-
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.
-
10.1038/ng.2454, 23143600
-
Lemmers RJ, Tawil R, Petek LM, Balog J, Block GJ, Santen GW, Amell AM, van der Vliet PJ, Almomani R, Straasheijm KR, Krom YD, Klooster R, Sun Y, Den Dunnen JT, Helmer Q, Donlin-Smith CM, Padberg GW, van Engelen BG, de Greef JC, Aartsma-Rus AM, Frants RR, de Visser M, Desnuelle C, Sacconi S, Filippova GN, Bakker B, Bamshad MJ, Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2. Nat Genet 2012, 44:1370-1374. 10.1038/ng.2454, 23143600.
-
(2012)
Nat Genet
, vol.44
, pp. 1370-1374
-
-
Lemmers, R.J.1
Tawil, R.2
Petek, L.M.3
Balog, J.4
Block, G.J.5
Santen, G.W.6
Amell, A.M.7
van der Vliet, P.J.8
Almomani, R.9
Straasheijm, K.R.10
Krom, Y.D.11
Klooster, R.12
Sun, Y.13
Den Dunnen, J.T.14
Helmer, Q.15
Donlin-Smith, C.M.16
Padberg, G.W.17
van Engelen, B.G.18
de Greef, J.C.19
Aartsma-Rus, A.M.20
Frants, R.R.21
de Visser, M.22
Desnuelle, C.23
Sacconi, S.24
Filippova, G.N.25
Bakker, B.26
Bamshad, M.J.27
Tapscott, S.J.28
Miller, D.G.29
van der Maarel, S.M.30
more..
-
3
-
-
84870507885
-
Digenic inheritance and Mendelian disease.
-
10.1038/ng.2479, 23192179
-
Lupski JR. Digenic inheritance and Mendelian disease. Nat Genet 2012, 44:1291-1292. 10.1038/ng.2479, 23192179.
-
(2012)
Nat Genet
, vol.44
, pp. 1291-1292
-
-
Lupski, J.R.1
-
4
-
-
84865208871
-
Rate of de novo mutations and the importance of father's age to disease risk.
-
10.1038/nature11396, 22914163
-
Kong A, Frigge ML, Masson G, Besenbacher S, Sulem P, Magnusson G, Gudjonsson SA, Sigurdsson A, Jonasdottir A, Jonasdottir A, Wong WS, Sigurdsson G, Walters GB, Steinberg S, Helgason H, Thorleifsson G, Gudbjartsson DF, Helgason A, Magnusson OT, Thorsteinsdottir U, Stefansson K. Rate of de novo mutations and the importance of father's age to disease risk. Nature 2012, 488:471-475. 10.1038/nature11396, 22914163.
-
(2012)
Nature
, vol.488
, pp. 471-475
-
-
Kong, A.1
Frigge, M.L.2
Masson, G.3
Besenbacher, S.4
Sulem, P.5
Magnusson, G.6
Gudjonsson, S.A.7
Sigurdsson, A.8
Jonasdottir, A.9
Jonasdottir, A.10
Wong, W.S.11
Sigurdsson, G.12
Walters, G.B.13
Steinberg, S.14
Helgason, H.15
Thorleifsson, G.16
Gudbjartsson, D.F.17
Helgason, A.18
Magnusson, O.T.19
Thorsteinsdottir, U.20
Stefansson, K.21
more..
-
5
-
-
84873030486
-
Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome.
-
doi: 10.1093/hmg/dds482
-
Sun Z, Liu P, Jia X, Withers MA, Jin L, Lupski JR, Zhang F. Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome. Hum Mol Genet 2012, doi: 10.1093/hmg/dds482.
-
(2012)
Hum Mol Genet
-
-
Sun, Z.1
Liu, P.2
Jia, X.3
Withers, M.A.4
Jin, L.5
Lupski, J.R.6
Zhang, F.7
-
6
-
-
84868214089
-
Estimating the human mutation rate using autozygosity in a founder population.
-
10.1038/ng.2418, 23001126
-
Campbell CD, Chong JX, Malig M, Ko A, Dumont BL, Han L, Vives L, O'Roak BJ, Sudmant PH, Shendure J, Abney M, Ober C, Eichler EE. Estimating the human mutation rate using autozygosity in a founder population. Nat Genet 2012, 44:1277-1281. 10.1038/ng.2418, 23001126.
-
(2012)
Nat Genet
, vol.44
, pp. 1277-1281
-
-
Campbell, C.D.1
Chong, J.X.2
Malig, M.3
Ko, A.4
Dumont, B.L.5
Han, L.6
Vives, L.7
O'Roak, B.J.8
Sudmant, P.H.9
Shendure, J.10
Abney, M.11
Ober, C.12
Eichler, E.E.13
-
7
-
-
84868244955
-
Older males beget more mutations.
-
10.1038/ng.2448, 23104062
-
Hurles M. Older males beget more mutations. Nat Genet 2012, 44:1174-1176. 10.1038/ng.2448, 23104062.
-
(2012)
Nat Genet
, vol.44
, pp. 1174-1176
-
-
Hurles, M.1
-
8
-
-
84868543309
-
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
-
10.1016/S0140-6736(12)61480-9, 23020937
-
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet 2012, 380:1674-1682. 10.1016/S0140-6736(12)61480-9, 23020937.
-
(2012)
Lancet
, vol.380
, pp. 1674-1682
-
-
Rauch, A.1
Wieczorek, D.2
Graf, E.3
Wieland, T.4
Endele, S.5
Schwarzmayr, T.6
Albrecht, B.7
Bartholdi, D.8
Beygo, J.9
Di Donato, N.10
Dufke, A.11
Cremer, K.12
Hempel, M.13
Horn, D.14
Hoyer, J.15
Joset, P.16
Röpke, A.17
Moog, U.18
Riess, A.19
Thiel, C.T.20
Tzschach, A.21
Wiesener, A.22
Wohlleber, E.23
Zweier, C.24
Ekici, A.B.25
Zink, A.M.26
Rump, A.27
Meisinger, C.28
Grallert, H.29
Sticht, H.30
more..
-
9
-
-
84868686559
-
Diagnostic exome sequencing in persons with severe intellectual disability.
-
10.1056/NEJMoa1206524, 23033978
-
de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, del Rosario M, Hoischen A, Scheffer H, de Vries BB, Brunner HG, Veltman JA, Vissers LE. Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med 2012, 367:1921-1929. 10.1056/NEJMoa1206524, 23033978.
-
(2012)
N Engl J Med
, vol.367
, pp. 1921-1929
-
-
de Ligt, J.1
Willemsen, M.H.2
van Bon, B.W.3
Kleefstra, T.4
Yntema, H.G.5
Kroes, T.6
Vulto-van Silfhout, A.T.7
Koolen, D.A.8
de Vries, P.9
Gilissen, C.10
del Rosario, M.11
Hoischen, A.12
Scheffer, H.13
de Vries, B.B.14
Brunner, H.G.15
Veltman, J.A.16
Vissers, L.E.17
-
10
-
-
84873308075
-
Office of Public Health Genomics, Centers for Disease Control and Prevention.
-
Office of Public Health Genomics, Centers for Disease Control and Prevention. , http://www.cdc.gov/genomics/
-
-
-
-
11
-
-
84873290613
-
PHG Foundation: Translating genomics: making science work for health.
-
PHG Foundation: Translating genomics: making science work for health. , http://www.phgfoundation.org/15years/
-
-
-
-
12
-
-
84873285198
-
Public Health Genomics European Network.
-
Public Health Genomics European Network. , http://www.phgen.eu/typo3/index.php
-
-
-
-
13
-
-
78650646491
-
Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and 'personalized' medicine?.
-
10.1097/GIM.0b013e3182011222, 21189494
-
Burke W, Burton H, Hall AE, Karmali M, Khoury MJ, Knoppers B, Meslin EM, Stanley F, Wright CF, Zimmern RL. Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and 'personalized' medicine?. Genet Med 2010, 12:785-791. 10.1097/GIM.0b013e3182011222, 21189494.
-
(2010)
Genet Med
, vol.12
, pp. 785-791
-
-
Burke, W.1
Burton, H.2
Hall, A.E.3
Karmali, M.4
Khoury, M.J.5
Knoppers, B.6
Meslin, E.M.7
Stanley, F.8
Wright, C.F.9
Zimmern, R.L.10
-
14
-
-
84870197973
-
Epidemiology. Outsmarting outbreaks.
-
10.1126/science.1232327, 23197523
-
Walker MJ, Beatson SA. Epidemiology. Outsmarting outbreaks. Science 2012, 338:1161-1162. 10.1126/science.1232327, 23197523.
-
(2012)
Science
, vol.338
, pp. 1161-1162
-
-
Walker, M.J.1
Beatson, S.A.2
-
15
-
-
85041176360
-
Translational genetics: whole-genome sequencing diagnostics for newborns.
-
Flintoft L. Translational genetics: whole-genome sequencing diagnostics for newborns. Nat Rev Genet 2012, 13:758.
-
(2012)
Nat Rev Genet
, vol.13
, pp. 758
-
-
Flintoft, L.1
-
16
-
-
84873309581
-
-
Centers for Disease Control and Prevention
-
Centers for Disease Control and Prevention Genomic Tests and Family History by Levels of Evidence Centers for Disease Control and Prevention., http://www.cdc.gov/genomics/gtesting/tier.htm
-
Genomic Tests and Family History by Levels of Evidence
-
-
-
17
-
-
84870789057
-
Public Health Action in Genomics Is Now Needed beyond Newborn Screening.
-
10.1159/000341889, 22986915
-
Bowen MS, Kolor K, Dotson WD, Ned RM, Khoury MJ. Public Health Action in Genomics Is Now Needed beyond Newborn Screening. Public Health Genomics 2012, 15:327-334. 10.1159/000341889, 22986915.
-
(2012)
Public Health Genomics
, vol.15
, pp. 327-334
-
-
Bowen, M.S.1
Kolor, K.2
Dotson, W.D.3
Ned, R.M.4
Khoury, M.J.5
-
18
-
-
0033168459
-
Shattuck lecture--medical and societal consequences of the Human Genome Project.
-
10.1056/NEJM199907013410106, 10387940
-
Collins FS. Shattuck lecture--medical and societal consequences of the Human Genome Project. N Engl J Med 1999, 341:28-37. 10.1056/NEJM199907013410106, 10387940.
-
(1999)
N Engl J Med
, vol.341
, pp. 28-37
-
-
Collins, F.S.1
-
19
-
-
84873279922
-
PharmGKB: IL28B.
-
PharmGKB: IL28B. , http://www.pharmgkb.org/gene/PA134952671
-
-
-
-
20
-
-
84874116578
-
Innate immunity and HCV.
-
doi: 10.1016/j.jhep.2012.10.005
-
Heim MH. Innate immunity and HCV. J Hepatol 2012, doi: 10.1016/j.jhep.2012.10.005.
-
(2012)
J Hepatol
-
-
Heim, M.H.1
-
21
-
-
84867120437
-
Cystic fibrosis in an era of genomically guided therapy.
-
10.1093/hmg/dds345, 22914736
-
Barrett PM, Alagely A, Topol EJ. Cystic fibrosis in an era of genomically guided therapy. Hum Mol Genet 2012, 21:R66-R71. 10.1093/hmg/dds345, 22914736.
-
(2012)
Hum Mol Genet
, vol.21
-
-
Barrett, P.M.1
Alagely, A.2
Topol, E.J.3
-
22
-
-
84872248328
-
Omics and drug response.
-
10.1146/annurev-pharmtox-010510-100502, 23140244
-
Meyer UA, Zanger UM, Schwab M. Omics and drug response. Annu Rev Pharmacol Toxicol 2013, 53:475-502. 10.1146/annurev-pharmtox-010510-100502, 23140244.
-
(2013)
Annu Rev Pharmacol Toxicol
, vol.53
, pp. 475-502
-
-
Meyer, U.A.1
Zanger, U.M.2
Schwab, M.3
-
23
-
-
84870065830
-
Pharmacogenomics: a key component of personalized therapy.
-
10.1186/gm394, 23194652
-
Schwab M, Schaeffeler E. Pharmacogenomics: a key component of personalized therapy. Genome Med 2012, 4:93. 10.1186/gm394, 23194652.
-
(2012)
Genome Med
, vol.4
, pp. 93
-
-
Schwab, M.1
Schaeffeler, E.2
-
24
-
-
84855369410
-
Robust analysis of the yeast proteome under 50 kDa by molecular-mass-based fractionation and top-down mass spectrometry.
-
10.1021/ac202384v, 3262231, 22103811
-
Kellie JF, Catherman AD, Durbin KR, Tran JC, Tipton JD, Norris JL, Witkowski CE, Thomas PM, Kelleher NL. Robust analysis of the yeast proteome under 50 kDa by molecular-mass-based fractionation and top-down mass spectrometry. Anal Chem 2012, 84:209-215. 10.1021/ac202384v, 3262231, 22103811.
-
(2012)
Anal Chem
, vol.84
, pp. 209-215
-
-
Kellie, J.F.1
Catherman, A.D.2
Durbin, K.R.3
Tran, J.C.4
Tipton, J.D.5
Norris, J.L.6
Witkowski, C.E.7
Thomas, P.M.8
Kelleher, N.L.9
-
25
-
-
83055176451
-
Mapping intact protein isoforms in discovery mode using top-down proteomics.
-
10.1038/nature10575, 3237778, 22037311
-
Tran JC, Zamdborg L, Ahlf DR, Lee JE, Catherman AD, Durbin KR, Tipton JD, Vellaichamy A, Kellie JF, Li M, Wu C, Sweet SM, Early BP, Siuti N, LeDuc RD, Compton PD, Thomas PM, Kelleher NL. Mapping intact protein isoforms in discovery mode using top-down proteomics. Nature 2011, 480:254-258. 10.1038/nature10575, 3237778, 22037311.
-
(2011)
Nature
, vol.480
, pp. 254-258
-
-
Tran, J.C.1
Zamdborg, L.2
Ahlf, D.R.3
Lee, J.E.4
Catherman, A.D.5
Durbin, K.R.6
Tipton, J.D.7
Vellaichamy, A.8
Kellie, J.F.9
Li, M.10
Wu, C.11
Sweet, S.M.12
Early, B.P.13
Siuti, N.14
LeDuc, R.D.15
Compton, P.D.16
Thomas, P.M.17
Kelleher, N.L.18
-
26
-
-
84864818817
-
Revolutionizing medicine in the 21st century through systems approaches.
-
10.1002/biot.201100306, 22815171
-
Hood L, Balling R, Auffray C. Revolutionizing medicine in the 21st century through systems approaches. Biotechnol J 2012, 7:992-1001. 10.1002/biot.201100306, 22815171.
-
(2012)
Biotechnol J
, vol.7
, pp. 992-1001
-
-
Hood, L.1
Balling, R.2
Auffray, C.3
-
27
-
-
84871313456
-
Genomewide association studies and common disease--realizing clinical utility.
-
10.1056/NEJMp1212285, 23252523
-
Fugger L, McVean G, Bell JI. Genomewide association studies and common disease--realizing clinical utility. N Engl J Med 2012, 367:2370-2371. 10.1056/NEJMp1212285, 23252523.
-
(2012)
N Engl J Med
, vol.367
, pp. 2370-2371
-
-
Fugger, L.1
McVean, G.2
Bell, J.I.3
-
28
-
-
78651394465
-
Bring on the biomarkers.
-
10.1038/469156a, 21228852
-
Poste G. Bring on the biomarkers. Nature 2011, 469:156-157. 10.1038/469156a, 21228852.
-
(2011)
Nature
, vol.469
, pp. 156-157
-
-
Poste, G.1
-
29
-
-
84858433310
-
Personal omics profiling reveals dynamic molecular and medical phenotypes.
-
10.1016/j.cell.2012.02.009, 22424236
-
Chen R, Mias GI, Li-Pook-Than J, Jiang L, Lam HY, Chen R, Miriami E, Karczewski KJ, Hariharan M, Dewey FE, Cheng Y, Clark MJ, Im H, Habegger L, Balasubramanian S, O'Huallachain M, Dudley JT, Hillenmeyer S, Haraksingh R, Sharon D, Euskirchen G, Lacroute P, Bettinger K, Boyle AP, Kasowski M, Grubert F, Seki S, Garcia M, Whirl-Carrillo M, Gallardo M, et al. Personal omics profiling reveals dynamic molecular and medical phenotypes. Cell 2012, 148:1293-1307. 10.1016/j.cell.2012.02.009, 22424236.
-
(2012)
Cell
, vol.148
, pp. 1293-1307
-
-
Chen, R.1
Mias, G.I.2
Li-Pook-Than, J.3
Jiang, L.4
Lam, H.Y.5
Chen, R.6
Miriami, E.7
Karczewski, K.J.8
Hariharan, M.9
Dewey, F.E.10
Cheng, Y.11
Clark, M.J.12
Im, H.13
Habegger, L.14
Balasubramanian, S.15
O'Huallachain, M.16
Dudley, J.T.17
Hillenmeyer, S.18
Haraksingh, R.19
Sharon, D.20
Euskirchen, G.21
Lacroute, P.22
Bettinger, K.23
Boyle, A.P.24
Kasowski, M.25
Grubert, F.26
Seki, S.27
Garcia, M.28
Whirl-Carrillo, M.29
Gallardo, M.30
more..
-
30
-
-
84864806354
-
Quantifying your body: a how-to guide from a systems biology perspective.
-
10.1002/biot.201100495, 22887886
-
Smarr L. Quantifying your body: a how-to guide from a systems biology perspective. Biotechnol J 2012, 7:980-991. 10.1002/biot.201100495, 22887886.
-
(2012)
Biotechnol J
, vol.7
, pp. 980-991
-
-
Smarr, L.1
-
31
-
-
84879409324
-
The COPD control panel: towards personalised medicine in COPD.
-
doi:10.1136/thoraxjnl-2012-202772
-
Agusti A, Macnee W. The COPD control panel: towards personalised medicine in COPD. Thorax 2012, doi:10.1136/thoraxjnl-2012-202772.
-
(2012)
Thorax
-
-
Agusti, A.1
Macnee, W.2
-
32
-
-
84864797353
-
Editorial: Systems biology and personalized medicine - the future is now.
-
10.1002/biot.201200242, 22887882
-
Auffray C, Hood L. Editorial: Systems biology and personalized medicine - the future is now. Biotechnol J 2012, 7:938-939. 10.1002/biot.201200242, 22887882.
-
(2012)
Biotechnol J
, vol.7
, pp. 938-939
-
-
Auffray, C.1
Hood, L.2
-
33
-
-
84870568851
-
Clinical diagnosis by whole-genome sequencing of a prenatal sample.
-
10.1056/NEJMoa1208594, 23215558
-
Talkowski ME, Ordulu Z, Pillalamarri V, Benson CB, Blumenthal I, Connolly S, Hanscom C, Hussain N, Pereira S, Picker J, Rosenfeld JA, Shaffer LG, Wilkins-Haug LE, Gusella JF, Morton CC. Clinical diagnosis by whole-genome sequencing of a prenatal sample. N Engl J Med 2012, 367:2226-2232. 10.1056/NEJMoa1208594, 23215558.
-
(2012)
N Engl J Med
, vol.367
, pp. 2226-2232
-
-
Talkowski, M.E.1
Ordulu, Z.2
Pillalamarri, V.3
Benson, C.B.4
Blumenthal, I.5
Connolly, S.6
Hanscom, C.7
Hussain, N.8
Pereira, S.9
Picker, J.10
Rosenfeld, J.A.11
Shaffer, L.G.12
Wilkins-Haug, L.E.13
Gusella, J.F.14
Morton, C.C.15
-
34
-
-
83055182072
-
Next-generation DNA sequencing, regulation, and the limits of paternalism: the next challenge.
-
10.1001/jama.2011.1788, 22147382
-
Evans JP, Berg JS. Next-generation DNA sequencing, regulation, and the limits of paternalism: the next challenge. JAMA 2011, 306:2376-2377. 10.1001/jama.2011.1788, 22147382.
-
(2011)
JAMA
, vol.306
, pp. 2376-2377
-
-
Evans, J.P.1
Berg, J.S.2
-
35
-
-
84873300709
-
Why Cheaper Genetic Testing Could Cost Us a Fortune.
-
Rochman B. Why Cheaper Genetic Testing Could Cost Us a Fortune. Time 2012, , http://healthland.time.com/2012/10/26/why-cheaper-genetic-testing-could-cost-us-a-fortune/
-
(2012)
Time
-
-
Rochman, B.1
-
37
-
-
84873280761
-
Privacy and whole genome sequencing.
-
Gutmann A. Privacy and whole genome sequencing. Reuters 2012, , http://blogs.reuters.com/great-debate/2012/10/11/privacy-and-whole-genome-sequencing/
-
(2012)
Reuters
-
-
Gutmann, A.1
-
38
-
-
84872450521
-
Privacy and Progress in Whole Genome Sequencing.
-
Presidential Commission for the Study of Bioethical Issues
-
Presidential Commission for the Study of Bioethical Issues Privacy and Progress in Whole Genome Sequencing. 2012, Presidential Commission for the Study of Bioethical Issues., http://www.bioethics.gov/cms/node/764
-
(2012)
-
-
-
39
-
-
84868309115
-
Genetic tests: Politics and fetal diagnostics collide.
-
King JS. Genetic tests: Politics and fetal diagnostics collide. Nature 2012, 491:3334.
-
(2012)
Nature
, vol.491
, pp. 3334
-
-
King, J.S.1
-
40
-
-
84873302282
-
World Changing Ideas 2012.
-
The Editors
-
The Editors World Changing Ideas 2012. Sci Am 2012, The Editors., http://www.scientificamerican.com/article.cfm?id=world-changing-ideas-2012-innovations-radical-enough-alter-lives
-
(2012)
Sci Am
-
-
-
41
-
-
84873318262
-
The American College of Obstetricians and Gynecologists Committee on Genetics and The Society for Maternal-Fetal Medicine Publications Committee. Noninvasive Prenatal Testing for Fetal Aneuploidy: Committee Opinion.
-
Number 545, December 2012
-
The American College of Obstetricians and Gynecologists Committee on Genetics and The Society for Maternal-Fetal Medicine Publications Committee. Noninvasive Prenatal Testing for Fetal Aneuploidy: Committee Opinion. Number 545, December 2012 [http://www.acog.org/Resources_And_Publications/Committee_Opinions/Committee_on_Genetics/Noninvasive_Prenatal_Testing_for_Fetal_Aneuploidy.
-
-
-
|