-
1
-
-
27244437783
-
Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers
-
Abecasis G.R., Wigginton J.E. Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. Am. J. Hum. Genet. 2005, 77:754-767.
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 754-767
-
-
Abecasis, G.R.1
Wigginton, J.E.2
-
2
-
-
0014357975
-
Probable assignment of the Duffy blood group locus to chromosome 1 in man
-
Donahue R.P., Bias W.B., Renwick J.H., McKusick V.A. Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc. Natl. Acad. Sci. U.S.A. 1968, 61:949-955.
-
(1968)
Proc. Natl. Acad. Sci. U.S.A.
, vol.61
, pp. 949-955
-
-
Donahue, R.P.1
Bias, W.B.2
Renwick, J.H.3
McKusick, V.A.4
-
3
-
-
0025574865
-
Identifying human disease genes by positional cloning
-
Collins F.S. Identifying human disease genes by positional cloning. Harvey Lect. 1990, 86:149-164.
-
(1990)
Harvey Lect.
, vol.86
, pp. 149-164
-
-
Collins, F.S.1
-
4
-
-
0024424270
-
Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA
-
Riordan J.R., Rommens J.M., Kerem B., Alon N., Rozmahel R., Grzelczak Z., Zielenski J., Lok S., Plavsic N., Chou J.L., et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 1989, 245:1066-1073.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.L.10
-
6
-
-
0016302483
-
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies
-
Ott J. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am. J. Hum. Genet. 1974, 26:588-597.
-
(1974)
Am. J. Hum. Genet.
, vol.26
, pp. 588-597
-
-
Ott, J.1
-
7
-
-
0024190141
-
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
-
Lange K., Weeks D., Boehnke M. Programs for pedigree analysis: MENDEL, FISHER, and dGENE. Genet. Epidemiol. 1988, 5:471-472.
-
(1988)
Genet. Epidemiol.
, vol.5
, pp. 471-472
-
-
Lange, K.1
Weeks, D.2
Boehnke, M.3
-
9
-
-
0029886532
-
Parametric and nonparametric linkage analysis: a unified multipoint approach
-
Kruglyak L., Daly M.J., Reeve-Daly M.P., Lander E.S. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am. J. Hum. Genet. 1996, 58:1347-1363.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
10
-
-
80052709095
-
Chromosomal haplotypes by genetic phasing of human families
-
Roach J.C., Glusman G., Hubley R., Montsaroff S.Z., Holloway A.K., Mauldin D.E., Srivastava D., Garg V., Pollard K.S., Galas D.J., Hood L., Smit A.F. Chromosomal haplotypes by genetic phasing of human families. Am. J. Hum. Genet. 2011, 89:382-397.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 382-397
-
-
Roach, J.C.1
Glusman, G.2
Hubley, R.3
Montsaroff, S.Z.4
Holloway, A.K.5
Mauldin, D.E.6
Srivastava, D.7
Garg, V.8
Pollard, K.S.9
Galas, D.J.10
Hood, L.11
Smit, A.F.12
-
11
-
-
77951799158
-
Analysis of genetic inheritance in a family quartet by whole-genome sequencing
-
Roach J.C., Glusman G., Smit A.F., Huff C.D., Hubley R., Shannon P.T., Rowen L., Pant K.P., Goodman N., Bamshad M., Shendure J., Drmanac R., Jorde L.B., Hood L., Galas D.J. Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science 2010, 328:636-639.
-
(2010)
Science
, vol.328
, pp. 636-639
-
-
Roach, J.C.1
Glusman, G.2
Smit, A.F.3
Huff, C.D.4
Hubley, R.5
Shannon, P.T.6
Rowen, L.7
Pant, K.P.8
Goodman, N.9
Bamshad, M.10
Shendure, J.11
Drmanac, R.12
Jorde, L.B.13
Hood, L.14
Galas, D.J.15
-
12
-
-
80052833627
-
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
-
Smith K.R., Bromhead C.J., Hildebrand M.S., Shearer A.E., Lockhart P.J., Najmabadi H., Leventer R.J., McGillivray G., Amor D.J., Smith R.J., Bahlo M. Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes. Genome Biol. 2011, 12:R85.
-
(2011)
Genome Biol.
, vol.12
-
-
Smith, K.R.1
Bromhead, C.J.2
Hildebrand, M.S.3
Shearer, A.E.4
Lockhart, P.J.5
Najmabadi, H.6
Leventer, R.J.7
McGillivray, G.8
Amor, D.J.9
Smith, R.J.10
Bahlo, M.11
-
13
-
-
65449170412
-
Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data
-
Jiang H., Orr A., Guernsey D.L., Robitaille J., Asselin G., Samuels M.E., Dube M.P. Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data. PLoS One 2009, 4:e5280.
-
(2009)
PLoS One
, vol.4
-
-
Jiang, H.1
Orr, A.2
Guernsey, D.L.3
Robitaille, J.4
Asselin, G.5
Samuels, M.E.6
Dube, M.P.7
-
14
-
-
36949027158
-
Direct inference of SNP heterozygosity rates and resolution of LOH detection
-
Li X., Self S.G., Galipeau P.C., Paulson T.G., Reid B.J. Direct inference of SNP heterozygosity rates and resolution of LOH detection. PLoS Comput. Biol. 2007, 3:e244.
-
(2007)
PLoS Comput. Biol.
, vol.3
-
-
Li, X.1
Self, S.G.2
Galipeau, P.C.3
Paulson, T.G.4
Reid, B.J.5
-
15
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A., Gudbjartsson D.F., Sainz J., Jonsdottir G.M., Gudjonsson S.A., Richardsson B., Sigurdardottir S., Barnard J., Hallbeck B., Masson G., Shlien A., Palsson S.T., Frigge M.L., Thorgeirsson T.E., Gulcher J.R., Stefansson K. A high-resolution recombination map of the human genome. Nat. Genet. 2002, 31:241-247.
-
(2002)
Nat. Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
Shlien, A.11
Palsson, S.T.12
Frigge, M.L.13
Thorgeirsson, T.E.14
Gulcher, J.R.15
Stefansson, K.16
-
16
-
-
44349116185
-
Mapping functions
-
Tan Y.D., Fornage M. Mapping functions. Genetica 2008, 133:235-246.
-
(2008)
Genetica
, vol.133
, pp. 235-246
-
-
Tan, Y.D.1
Fornage, M.2
-
17
-
-
35348983887
-
A second generation human haplotype map of over 3.1million SNPs
-
Frazer K.A., Ballinger D.G., Cox D.R., Hinds D.A., Stuve L.L., Gibbs R.A., Belmont J.W., Boudreau A., Hardenbol P., Leal S.M., Pasternak S., Wheeler D.A., Willis T.D., Yu F., Yang H., Zeng C., Gao Y., Hu H., Hu W., Li C., Lin W., Liu S., Pan H., Tang X., Wang J., Wang W., Yu J., Zhang B., Zhang Q., Zhao H., Zhou J., Gabriel S.B., Barry R., Blumenstiel B., Camargo A., Defelice M., Faggart M., Goyette M., Gupta S., Moore J., Nguyen H., Onofrio R.C., Parkin M., Roy J., Stahl E., Winchester E., Ziaugra L., Altshuler D., Shen Y., Yao Z., Huang W., Chu X., He Y., Jin L., Liu Y., Sun W., Wang H., Wang Y., Xiong X., Xu L., Waye M.M., Tsui S.K., Xue H., Wong J.T., Galver L.M., Fan J.B., Gunderson K., Murray S.S., Oliphant A.R., Chee M.S., Montpetit A., Chagnon F., Ferretti V., Leboeuf M., Olivier J.F., Phillips M.S., Roumy S., Sallee C., Verner A., Hudson T.J., Kwok P.Y., Cai D., Koboldt D.C., Miller R.D., Pawlikowska L., Taillon-Miller P., Xiao M., Tsui L.C., Mak W., Song Y.Q., Tam P.K., Nakamura Y., Kawaguchi T., Kitamoto T., Morizono T., Nagashima A., Ohnishi Y., Sekine A., Tanaka T., Tsunoda T., Deloukas P., Bird C.P., Delgado M., Dermitzakis E.T., Gwilliam R., Hunt S., Morrison J., Powell D., Stranger B.E., Whittaker P., Bentley D.R., Daly M.J., de Bakker P.I., Barrett J., Chretien Y.R., Maller J., McCarroll S., Patterson N., Pe'er I., Price A., Purcell S., Richter D.J., Sabeti P., Saxena R., Schaffner S.F., Sham P.C., Varilly P., Stein L.D., Krishnan L., Smith A.V., Tello-Ruiz M.K., Thorisson G.A., Chakravarti A., Chen P.E., Cutler D.J., Kashuk C.S., Lin S., Abecasis G.R., Guan W., Li Y., Munro H.M., Qin Z.S., Thomas D.J., McVean G., Auton A., Bottolo L., Cardin N., Eyheramendy S., Freeman C., Marchini J., Myers S., Spencer C., Stephens M., Donnelly P., Cardon L.R., Clarke G., Evans D.M., Morris A.P., Weir B.S., Mullikin J.C., Sherry S.T., Feolo M., Skol A., Zhang H., Matsuda I., Fukushima Y., Macer D.R., Suda E., Rotimi C.N., Adebamowo C.A., Ajayi I., Aniagwu T., Marshall P.A., Nkwodimmah C., Royal C.D., Leppert M.F., Dixon M., Peiffer A., Qiu R., Kent A., Kato K., Niikawa N., Adewole I.F., Knoppers B.M., Foster M.W., Clayton E.W., Watkin J., Muzny D., Nazareth L., Sodergren E., Weinstock G.M., Yakub I., Birren B.W., Wilson R.K., Fulton L.L., Rogers J., Burton J., Carter N.P., Clee C.M., Griffiths M., Jones M.C., McLay K., Plumb R.W., Ross M.T., Sims S.K., Willey D.L., Chen Z., Han H., Kang L., Godbout M., Wallenburg J.C., L'Archeveque P., Bellemare G., Saeki K., An D., Fu H., Li Q., Wang Z., Wang R., Holden A.L., Brooks L.D., McEwen J.E., Guyer M.S., Wang V.O., Peterson J.L., Shi M., Spiegel J., Sung L.M., Zacharia L.F., Collins F.S., Kennedy K., Jamieson R., Stewart J. A second generation human haplotype map of over 3.1million SNPs. Nature 2007, 449:851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
Pasternak, S.11
Wheeler, D.A.12
Willis, T.D.13
Yu, F.14
Yang, H.15
Zeng, C.16
Gao, Y.17
Hu, H.18
Hu, W.19
Li, C.20
Lin, W.21
Liu, S.22
Pan, H.23
Tang, X.24
Wang, J.25
Wang, W.26
Yu, J.27
Zhang, B.28
Zhang, Q.29
Zhao, H.30
Zhou, J.31
Gabriel, S.B.32
Barry, R.33
Blumenstiel, B.34
Camargo, A.35
Defelice, M.36
Faggart, M.37
Goyette, M.38
Gupta, S.39
Moore, J.40
Nguyen, H.41
Onofrio, R.C.42
Parkin, M.43
Roy, J.44
Stahl, E.45
Winchester, E.46
Ziaugra, L.47
Altshuler, D.48
Shen, Y.49
Yao, Z.50
Huang, W.51
Chu, X.52
He, Y.53
Jin, L.54
Liu, Y.55
Sun, W.56
Wang, H.57
Wang, Y.58
Xiong, X.59
Xu, L.60
Waye, M.M.61
Tsui, S.K.62
Xue, H.63
Wong, J.T.64
Galver, L.M.65
Fan, J.B.66
Gunderson, K.67
Murray, S.S.68
Oliphant, A.R.69
Chee, M.S.70
Montpetit, A.71
Chagnon, F.72
Ferretti, V.73
Leboeuf, M.74
Olivier, J.F.75
Phillips, M.S.76
Roumy, S.77
Sallee, C.78
Verner, A.79
Hudson, T.J.80
Kwok, P.Y.81
Cai, D.82
Koboldt, D.C.83
Miller, R.D.84
Pawlikowska, L.85
Taillon-Miller, P.86
Xiao, M.87
Tsui, L.C.88
Mak, W.89
Song, Y.Q.90
Tam, P.K.91
Nakamura, Y.92
Kawaguchi, T.93
Kitamoto, T.94
Morizono, T.95
Nagashima, A.96
Ohnishi, Y.97
Sekine, A.98
Tanaka, T.99
more..
-
18
-
-
79551565257
-
NT5E mutations and arterial calcifications
-
St Hilaire C., Ziegler S.G., Markello T.C., Brusco A., Groden C., Gill F., Carlson-Donohoe H., Lederman R.J., Chen M.Y., Yang D., Siegenthaler M.P., Arduino C., Mancini C., Freudenthal B., Stanescu H.C., Zdebik A.A., Chaganti R.K., Nussbaum R.L., Kleta R., Gahl W.A., Boehm M. NT5E mutations and arterial calcifications. N. Eng. J. Med. 2011, 364:432-442.
-
(2011)
N. Eng. J. Med.
, vol.364
, pp. 432-442
-
-
St Hilaire, C.1
Ziegler, S.G.2
Markello, T.C.3
Brusco, A.4
Groden, C.5
Gill, F.6
Carlson-Donohoe, H.7
Lederman, R.J.8
Chen, M.Y.9
Yang, D.10
Siegenthaler, M.P.11
Arduino, C.12
Mancini, C.13
Freudenthal, B.14
Stanescu, H.C.15
Zdebik, A.A.16
Chaganti, R.K.17
Nussbaum, R.L.18
Kleta, R.19
Gahl, W.A.20
Boehm, M.21
more..
-
19
-
-
70349659703
-
Genetic analysis of variation in human meiotic recombination
-
Chowdhury R., Bois P.R.J., Feingold E., Sherman S.L., Cheung VG V.G. Genetic analysis of variation in human meiotic recombination. PLoS Genetics 2005, e1000648.
-
(2005)
PLoS Genetics
-
-
Chowdhury, R.1
Bois, P.R.J.2
Feingold, E.3
Sherman, S.L.4
Cheung Vg, V.G.5
-
20
-
-
26844482093
-
A fine-scale map of recombination rates and hotspots across the human genome
-
Meyers S., Bottolo L., Freeman C., McVean G., Donnell P. A fine-scale map of recombination rates and hotspots across the human genome. Science 2005, 310:321-324.
-
(2005)
Science
, vol.310
, pp. 321-324
-
-
Meyers, S.1
Bottolo, L.2
Freeman, C.3
McVean, G.4
Donnell, P.5
-
21
-
-
33847216961
-
Polymorphic variation in human meiotic recombination
-
Cheung V.G., Burdick J.T., Hirschmann D., Morley M. Polymorphic variation in human meiotic recombination. Am. J. Hum. Genet. 2007, 80:526-530.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 526-530
-
-
Cheung, V.G.1
Burdick, J.T.2
Hirschmann, D.3
Morley, M.4
-
22
-
-
70349696278
-
Broad-scale recombination patterns underlying proper disjunction in humans
-
Fledel-Alon A., Wilson D.J., Broman K., Wen X., Ober C., Coop G., Przeworski M. Broad-scale recombination patterns underlying proper disjunction in humans. PLoS Genet. 2009, 5:e1000658.
-
(2009)
PLoS Genet.
, vol.5
-
-
Fledel-Alon, A.1
Wilson, D.J.2
Broman, K.3
Wen, X.4
Ober, C.5
Coop, G.6
Przeworski, M.7
-
23
-
-
79960239873
-
Progressive myoclonic epilepsy-associated gene KCTD7 is a regulator of potassium conductance in neurons
-
Azizieh R., Orduz D., Van Bogaert P., Bouschet T., Rodriguez W., Schiffmann S.N., Pirson I., Abramowicz M.J. Progressive myoclonic epilepsy-associated gene KCTD7 is a regulator of potassium conductance in neurons. Mol. Neurobiol. 2011, 44:111-121.
-
(2011)
Mol. Neurobiol.
, vol.44
, pp. 111-121
-
-
Azizieh, R.1
Orduz, D.2
Van Bogaert, P.3
Bouschet, T.4
Rodriguez, W.5
Schiffmann, S.N.6
Pirson, I.7
Abramowicz, M.J.8
-
24
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley D.R., Balasubramanian S., Swerdlow H.P., Smith G.P., Milton J., Brown C.G., Hall K.P., Evers D.J., Barnes C.L., Bignell H.R., Boutell J.M., Bryant J., Carter R.J., Keira Cheetham R., Cox A.J., Ellis D.J., Flatbush M.R., Gormley N.A., Humphray S.J., Irving L.J., Karbelashvili M.S., Kirk S.M., Li H., Liu X., Maisinger K.S., Murray L.J., Obradovic B., Ost T., Parkinson M.L., Pratt M.R., Rasolonjatovo I.M., Reed M.T., Rigatti R., Rodighiero C., Ross M.T., Sabot A., Sankar S.V., Scally A., Schroth G.P., Smith M.E., Smith V.P., Spiridou A., Torrance P.E., Tzonev S.S., Vermaas E.H., Walter K., Wu X., Zhang L., Alam M.D., Anastasi C., Aniebo I.C., Bailey D.M., Bancarz I.R., Banerjee S., Barbour S.G., Baybayan P.A., Benoit V.A., Benson K.F., Bevis C., Black P.J., Boodhun A., Brennan J.S., Bridgham J.A., Brown R.C., Brown A.A., Buermann D.H., Bundu A.A., Burrows J.C., Carter N.P., Castillo N., Chiara E.C.M., Chang S., Neil Cooley R., Crake N.R., Dada O.O., Diakoumakos K.D., Dominguez-Fernandez B., Earnshaw D.J., Egbujor U.C., Elmore D.W., Etchin S.S., Ewan M.R., Fedurco M., Fraser L.J., Fuentes Fajardo K.V., Scott Furey W., George D., Gietzen K.J., Goddard C.P., Golda G.S., Granieri P.A., Green D.E., Gustafson D.L., Hansen N.F., Harnish K., Haudenschild C.D., Heyer N.I., Hims M.M., Ho J.T., Horgan A.M., Hoschler K., Hurwitz S., Ivanov D.V., Johnson M.Q., James T., Huw Jones T.A., Kang G.D., Kerelska T.H., Kersey A.D., Khrebtukova I., Kindwall A.P., Kingsbury Z., Kokko-Gonzales P.I., Kumar A., Laurent M.A., Lawley C.T., Lee S.E., Lee X., Liao A.K., Loch J.A., Lok M., Luo S., Mammen R.M., Martin J.W., McCauley P.G., McNitt P., Mehta P., Moon K.W., Mullens J.W., Newington T., Ning Z., Ling Ng B., Novo S.M., O'Neill M.J., Osborne M.A., Osnowski A., Ostadan O., Paraschos L.L., Pickering L., Pike A.C., Chris Pinkard D., Pliskin D.P., Podhasky J., Quijano V.J., Raczy C., Rae V.H., Rawlings S.R., Chiva Rodriguez A., Roe P.M., Rogers J., Rogert Bacigalupo M.C., Romanov N., Romieu A., Roth R.K., Rourke N.J., Ruediger S.T., Rusman E., Sanches-Kuiper R.M., Schenker M.R., Seoane J.M., Shaw R.J., Shiver M.K., Short S.W., Sizto N.L., Sluis J.P., Smith M.A., Ernest Sohna Sohna J., Spence E.J., Stevens K., Sutton N., Szajkowski L., Tregidgo C.L., Turcatti G., Vandevondele S., Verhovsky Y., Virk S.M., Wakelin S., Walcott G.C., Wang J., Worsley G.J., Yan J., Yau L., Zuerlein M., Mullikin J.C., Hurles M.E., McCooke N.J., West J.S., Oaks F.L., Lundberg P.L., Klenerman D., Durbin R., Smith A.J. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008, 456:53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
Smith, G.P.4
Milton, J.5
Brown, C.G.6
Hall, K.P.7
Evers, D.J.8
Barnes, C.L.9
Bignell, H.R.10
Boutell, J.M.11
Bryant, J.12
Carter, R.J.13
Keira Cheetham, R.14
Cox, A.J.15
Ellis, D.J.16
Flatbush, M.R.17
Gormley, N.A.18
Humphray, S.J.19
Irving, L.J.20
Karbelashvili, M.S.21
Kirk, S.M.22
Li, H.23
Liu, X.24
Maisinger, K.S.25
Murray, L.J.26
Obradovic, B.27
Ost, T.28
Parkinson, M.L.29
Pratt, M.R.30
Rasolonjatovo, I.M.31
Reed, M.T.32
Rigatti, R.33
Rodighiero, C.34
Ross, M.T.35
Sabot, A.36
Sankar, S.V.37
Scally, A.38
Schroth, G.P.39
Smith, M.E.40
Smith, V.P.41
Spiridou, A.42
Torrance, P.E.43
Tzonev, S.S.44
Vermaas, E.H.45
Walter, K.46
Wu, X.47
Zhang, L.48
Alam, M.D.49
Anastasi, C.50
Aniebo, I.C.51
Bailey, D.M.52
Bancarz, I.R.53
Banerjee, S.54
Barbour, S.G.55
Baybayan, P.A.56
Benoit, V.A.57
Benson, K.F.58
Bevis, C.59
Black, P.J.60
Boodhun, A.61
Brennan, J.S.62
Bridgham, J.A.63
Brown, R.C.64
Brown, A.A.65
Buermann, D.H.66
Bundu, A.A.67
Burrows, J.C.68
Carter, N.P.69
Castillo, N.70
Chiara, E.C.M.71
Chang, S.72
Neil Cooley, R.73
Crake, N.R.74
Dada, O.O.75
Diakoumakos, K.D.76
Dominguez-Fernandez, B.77
Earnshaw, D.J.78
Egbujor, U.C.79
Elmore, D.W.80
Etchin, S.S.81
Ewan, M.R.82
Fedurco, M.83
Fraser, L.J.84
Fuentes Fajardo, K.V.85
Scott Furey, W.86
George, D.87
Gietzen, K.J.88
Goddard, C.P.89
Golda, G.S.90
Granieri, P.A.91
Green, D.E.92
Gustafson, D.L.93
Hansen, N.F.94
Harnish, K.95
Haudenschild, C.D.96
Heyer, N.I.97
Hims, M.M.98
Ho, J.T.99
more..
-
25
-
-
0032231941
-
PedCheck: a program for identification of genotype incompatibilities in linkage analysis
-
O'Connell J.R., Weeks D.E. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am. J. Hum. Genet. 1998, 63:259-266.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
26
-
-
27144455205
-
Allegro version 2
-
Gudbjartsson D.F., Thorvaldsson T., Kong A., Gunnarsson G., Ingolfsdottir A. Allegro version 2. Nat. Genet. 2005, 37:1015-1016.
-
(2005)
Nat. Genet.
, vol.37
, pp. 1015-1016
-
-
Gudbjartsson, D.F.1
Thorvaldsson, T.2
Kong, A.3
Gunnarsson, G.4
Ingolfsdottir, A.5
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