-
1
-
-
0034017850
-
GOLD - Graphical overview of linkage disequilibrium
-
Abecasis GR, Cookson WO. 2000. GOLD-graphical overview of linkage disequilibrium. Bioinformatics 16:182-183.
-
(2000)
Bioinformatics
, vol.16
, pp. 182-183
-
-
Abecasis, G.R.1
Cookson, W.O.2
-
2
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. 2002. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
3
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M. 1995. Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med 25:63-77.
-
(1995)
Psychol Med
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
4
-
-
0028020638
-
Effect of serotonin depletion on vibrissa-related patterns of thalamic afferents in the rat's somatosensory cortex
-
Bennett-Clarke CA, Leslie MJ, Lane RD, Rhoades RW. 1994. Effect of serotonin depletion on vibrissa-related patterns of thalamic afferents in the rat's somatosensory cortex. J Neurosci 14:7594-7607.
-
(1994)
J Neurosci
, vol.14
, pp. 7594-7607
-
-
Bennett-Clarke, C.A.1
Leslie, M.J.2
Lane, R.D.3
Rhoades, R.W.4
-
5
-
-
0026217294
-
A comparison of pattern formation by thalamocortical and serotonergic afferents in the rat barrel field cortex
-
Blue ME, Erzurumlu RS, Jhaveri S. 1991. A comparison of pattern formation by thalamocortical and serotonergic afferents in the rat barrel field cortex. Cereb Cortex 1:380-389.
-
(1991)
Cereb Cortex
, vol.1
, pp. 380-389
-
-
Blue, M.E.1
Erzurumlu, R.S.2
Jhaveri, S.3
-
6
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL. 2001. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 68:1514-1520.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
Lawlor, B.A.7
Fitzgerald, M.8
Greenberg, D.A.9
Davis, K.L.10
-
7
-
-
0030058732
-
Lack of barrels in the somatosensory cortex of monoamine oxidase A-deficient mice: Role of a serotonin excess during the critical period
-
Cases O, Vitalis T, Seif I, De Maeyer E, Sotelo C, Gaspar P. 1996. Lack of barrels in the somatosensory cortex of monoamine oxidase A-deficient mice: Role of a serotonin excess during the critical period. Neuron 16:297-307.
-
(1996)
Neuron
, vol.16
, pp. 297-307
-
-
Cases, O.1
Vitalis, T.2
Seif, I.3
De Maeyer, E.4
Sotelo, C.5
Gaspar, P.6
-
8
-
-
0034929626
-
A general and accurate approach for computing the statistical power of the transmission disequilibrium test for complex disease genes
-
Chen WM, Deng HW. 2001. A general and accurate approach for computing the statistical power of the transmission disequilibrium test for complex disease genes. Genet Epidemiol 21:53-67.
-
(2001)
Genet Epidemiol
, vol.21
, pp. 53-67
-
-
Chen, W.M.1
Deng, H.W.2
-
9
-
-
0030824236
-
Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys
-
Chugani DC, Muzik O, Rothermel R, Behen M, Chakraborty P, Mangner T, da Silva EA, Chugani HT. 1997. Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys. Ann Neurol 42:666-669.
-
(1997)
Ann Neurol
, vol.42
, pp. 666-669
-
-
Chugani, D.C.1
Muzik, O.2
Rothermel, R.3
Behen, M.4
Chakraborty, P.5
Mangner, T.6
Da Silva, E.A.7
Chugani, H.T.8
-
10
-
-
0032987647
-
Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children
-
Chugani DC, Muzik O, Behen M, Rothermel R, Janisse JJ, Lee J, Chugani HT. 1999. Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children. Ann Neurol 45:287-295.
-
(1999)
Ann Neurol
, vol.45
, pp. 287-295
-
-
Chugani, D.C.1
Muzik, O.2
Behen, M.3
Rothermel, R.4
Janisse, J.J.5
Lee, J.6
Chugani, H.T.7
-
11
-
-
0034952023
-
Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders
-
Comings DE. 2001. Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders. Ann N Y Acad Sci 931:50-83.
-
(2001)
Ann N Y Acad Sci
, vol.931
, pp. 50-83
-
-
Comings, D.E.1
-
12
-
-
0025818923
-
Clinical and genetic relationships between autism-pervasive developmental disorder and Tourette syndrome: A study of 19 cases
-
Comings DE, Comings BG. 1991. Clinical and genetic relationships between autism-pervasive developmental disorder and Tourette syndrome: A study of 19 cases. Am J Med Genet 39:180-191.
-
(1991)
Am J Med Genet
, vol.39
, pp. 180-191
-
-
Comings, D.E.1
Comings, B.G.2
-
13
-
-
0025976896
-
Human tryptophan oxygenase localized to 4q31: Possible implications for alcoholism and other behavioral disorders
-
Comings DE, Muhleman D, Dietz GW Jr, Donlon T. 1991. Human tryptophan oxygenase localized to 4q31: Possible implications for alcoholism and other behavioral disorders. Genomics 9:301-308.
-
(1991)
Genomics
, vol.9
, pp. 301-308
-
-
Comings, D.E.1
Muhleman, D.2
Dietz Jr., G.W.3
Donlon, T.4
-
14
-
-
9544223224
-
Exon and intron variants in the human tryptophan 2,3-dioxygenase gene: Potential association with Tourette syndrome, substance abuse, and other disorders
-
Comings DE, Gade R, Muhleman D, Chiu C, Wu S, To M, Spence M, Dietz G, Winn-Deen E, Rosenthal RJ, Lesieur HR, Rugle L, Sverd J, Ferry L, Johnson JP, MacMurray JP. 1996. Exon and intron variants in the human tryptophan 2,3-dioxygenase gene: Potential association with Tourette syndrome, substance abuse, and other disorders. Pharmacogenetics 6:307-318.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 307-318
-
-
Comings, D.E.1
Gade, R.2
Muhleman, D.3
Chiu, C.4
Wu, S.5
To, M.6
Spence, M.7
Dietz, G.8
Winn-Deen, E.9
Rosenthal, R.J.10
Lesieur, H.R.11
Rugle, L.12
Sverd, J.13
Ferry, L.14
Johnson, J.P.15
MacMurray, J.P.16
-
15
-
-
0023728919
-
Free serotonin in plasma: Autistic children and their first-degree relatives
-
Cook EH Jr, Leventhal BL, Freedman DX. 1988. Free serotonin in plasma: Autistic children and their first-degree relatives. Biol Psychiatry 24: 488-491.
-
(1988)
Biol Psychiatry
, vol.24
, pp. 488-491
-
-
Cook Jr., E.H.1
Leventhal, B.L.2
Freedman, D.X.3
-
16
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH Jr, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal BL. 1997. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 2:247-250.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook Jr., E.H.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Yan, S.5
Lincoln, A.6
Haas, R.7
Courchesne, E.8
Leventhal, B.L.9
-
17
-
-
0035399728
-
SNP association studies in Alzheimer's disease highlight problems for complex disease analysis
-
Emahazion T, Feuk L, Jobs M, Sawyer SL, Fredman D, St Clair D, Prince JA, Brookes AJ. 2001. SNP association studies in Alzheimer's disease highlight problems for complex disease analysis. Trends Genet 17:407-413.
-
(2001)
Trends Genet
, vol.17
, pp. 407-413
-
-
Emahazion, T.1
Feuk, L.2
Jobs, M.3
Sawyer, S.L.4
Fredman, D.5
St. Clair, D.6
Prince, J.A.7
Brookes, A.J.8
-
18
-
-
0020614686
-
Role of precursor availability in the control of monamine biosynthesis in brain
-
Fernstrom JD. 1983. Role of precursor availability in the control of monamine biosynthesis in brain. Physiol Rev 63:484-546.
-
(1983)
Physiol Rev
, vol.63
, pp. 484-546
-
-
Fernstrom, J.D.1
-
19
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein S, Rutter M. 1977. Infantile autism: A genetic study of 21 twin pairs. J Child Psychol Psychiatry 18:297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
20
-
-
0033799573
-
Apolipoprotein E variation at the sequence haplotype level: Implications for the origin and maintenance of a major human polymorphism
-
Fullerton SM, Clark AG, Weiss KM, Nickerson DA, Taylor SL, Stengard JH, Salomaa V, Vartiainen E, Perola M, Boerwinkle E, Sing CF. 2000. Apolipoprotein E variation at the sequence haplotype level: Implications for the origin and maintenance of a major human polymorphism. Am J Hum Genet 67:881-900.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 881-900
-
-
Fullerton, S.M.1
Clark, A.G.2
Weiss, K.M.3
Nickerson, D.A.4
Taylor, S.L.5
Stengard, J.H.6
Salomaa, V.7
Vartiainen, E.8
Perola, M.9
Boerwinkle, E.10
Sing, C.F.11
-
21
-
-
0034916325
-
The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions
-
Geschwind DH, Sowinski J, Lord C, Iversen P, Shestack J, Jones P, Ducat L, Spence SJ. 2001. The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions. Am J Hum Genet 69:463-466.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 463-466
-
-
Geschwind, D.H.1
Sowinski, J.2
Lord, C.3
Iversen, P.4
Shestack, J.5
Jones, P.6
Ducat, L.7
Spence, S.J.8
-
22
-
-
0027419999
-
Possible association of c-Harvey-Ras-1 (HRAS-1) marker with autism
-
Herault J, Perrot A, Barthelemy C, Buchler M, Cherpi C, Leboyer M, Sauvage D, Lelord G, Mallet J, Muh JP. 1993. Possible association of c-Harvey-Ras-1 (HRAS-1) marker with autism. Psychiatry Res 46:261-267.
-
(1993)
Psychiatry Res
, vol.46
, pp. 261-267
-
-
Herault, J.1
Perrot, A.2
Barthelemy, C.3
Buchler, M.4
Cherpi, C.5
Leboyer, M.6
Sauvage, D.7
Lelord, G.8
Mallet, J.9
Muh, J.P.10
-
23
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
IMGSAC. 2001. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 69:570-581.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 570-581
-
-
-
24
-
-
0034929664
-
Notes from the SNP vs. haplotype front
-
Judson R, Stephens JC. 2001. Notes from the SNP vs. haplotype front. Pharmacogenomics 2:7-10.
-
(2001)
Pharmacogenomics
, vol.2
, pp. 7-10
-
-
Judson, R.1
Stephens, J.C.2
-
25
-
-
0034105758
-
Mutation screening of human 5-HT(2B)receptor gene in early-onset obsessive-compulsive disorder
-
Kim SJ, Veenstra-VanderWeele J, Hanna GL, Gonen D, Leventhal BL, Cook EH Jr. 2000. Mutation screening of human 5-HT(2B)receptor gene in early-onset obsessive-compulsive disorder. Mol Cell Probes 14:47-52.
-
(2000)
Mol Cell Probes
, vol.14
, pp. 47-52
-
-
Kim, S.J.1
Veenstra-VanderWeele, J.2
Hanna, G.L.3
Gonen, D.4
Leventhal, B.L.5
Cook Jr., E.H.6
-
26
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poustka F, Benner A, Lesch KP, Poustka A. 1997. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 6:2233-2238.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
-
27
-
-
0033358557
-
A note on power approximations for the transmission/disequilibrium test
-
Knapp M. 1999. A note on power approximations for the transmission/disequilibrium test. Am J Hum Genet 64:1177-1185.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1177-1185
-
-
Knapp, M.1
-
28
-
-
0033569904
-
Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder
-
Lassig JP, Vachirasomtoon K, Hartzell K, Leventhal M, Courchesne E, Courchesne R, Lord C, Leventhal BL, Cook EH Jr. 1999. Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder. Am J Med Genet 88:472-475.
-
(1999)
Am J Med Genet
, vol.88
, pp. 472-475
-
-
Lassig, J.P.1
Vachirasomtoon, K.2
Hartzell, K.3
Leventhal, M.4
Courchesne, E.5
Courchesne, R.6
Lord, C.7
Leventhal, B.L.8
Cook Jr., E.H.9
-
29
-
-
0030772982
-
Tests for linkage and association in nuclear families
-
Martin ER, Kaplan NL, Weir BS. 1997. Tests for linkage and association in nuclear families. Am J Hum Genet 61:439-448.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 439-448
-
-
Martin, E.R.1
Kaplan, N.L.2
Weir, B.S.3
-
30
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
Martin ER, Monks SA, Warren LL, Kaplan NL. 2000. A test for linkage and association in general pedigrees: The pedigree disequilibrium test. Am J Hum Genet 67:146-154.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 146-154
-
-
Martin, E.R.1
Monks, S.A.2
Warren, L.L.3
Kaplan, N.L.4
-
31
-
-
0035076031
-
Correcting for a potential bias in the pedigree disequilibrium test
-
Martin ER, Bass MP, Kaplan NL. 2001. Correcting for a potential bias in the pedigree disequilibrium test. Am J Hum Genet 68:1065-1067.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1065-1067
-
-
Martin, E.R.1
Bass, M.P.2
Kaplan, N.L.3
-
32
-
-
0029805972
-
Effects of tryptophan depletion in drug-free adults with autistic disorder
-
McDougle CJ, Naylor ST, Cohen DJ, Aghajanian GK, Heninger GR, Price LH. 1996. Effects of tryptophan depletion in drug-free adults with autistic disorder. Arch Gen Psychiatry 53:993-1000.
-
(1996)
Arch Gen Psychiatry
, vol.53
, pp. 993-1000
-
-
McDougle, C.J.1
Naylor, S.T.2
Cohen, D.J.3
Aghajanian, G.K.4
Heninger, G.R.5
Price, L.H.6
-
33
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. 1998. PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63:259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
34
-
-
0029994393
-
Laminar development of the mouse barrel cortex: Effects of neurotoxins against monoamines
-
Osterheld-Haas MC, Hornung JP. 1996. Laminar development of the mouse barrel cortex: Effects of neurotoxins against monoamines. Exp Brain Res 110:183-195.
-
(1996)
Exp Brain Res
, vol.110
, pp. 183-195
-
-
Osterheld-Haas, M.C.1
Hornung, J.P.2
-
35
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Rastam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M, van Malldergerme L. 1999. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet 8:805-812.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
Penet, C.11
Feingold, J.12
Brice, A.13
Leboyer, M.14
Van Malldergerme, L.15
-
36
-
-
3042746413
-
Analysis of ten candidate genes in autism by association and linkage
-
Philippe A, Guilloud-Bataille M, Martinez M, Gillberg C, Rastam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Penet C, Feingold J, Brice A, Leboyer M. 2002. Analysis of ten candidate genes in autism by association and linkage. Am J Med Genet 114:125-128.
-
(2002)
Am J Med Genet
, vol.114
, pp. 125-128
-
-
Philippe, A.1
Guilloud-Bataille, M.2
Martinez, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Penet, C.10
Feingold, J.11
Brice, A.12
Leboyer, M.13
-
37
-
-
0033046371
-
Case-parents design for gene-environment interaction
-
Schaid DJ. 1999. Case-parents design for gene-environment interaction. Genet Epidemiol 16:261-273.
-
(1999)
Genet Epidemiol
, vol.16
, pp. 261-273
-
-
Schaid, D.J.1
-
38
-
-
18344374001
-
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
-
Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, Abramson RK, Wright HH, DeLong RG, Gilbert JR, Cuccaro ML, Pericak-Vance MA. 2002. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. Am J Hum Genet 70:1058-1061.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1058-1061
-
-
Shao, Y.1
Raiford, K.L.2
Wolpert, C.M.3
Cope, H.A.4
Ravan, S.A.5
Ashley-Koch, A.A.6
Abramson, R.K.7
Wright, H.H.8
DeLong, R.G.9
Gilbert, J.R.10
Cuccaro, M.L.11
Pericak-Vance, M.A.12
-
39
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. 1996. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
40
-
-
0029858544
-
The TDT and other family-based tests for linkage disequilibrium and association
-
Spielman RS, Ewens WJ. 1996. The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet 59:983-989.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 983-989
-
-
Spielman, R.S.1
Ewens, W.J.2
-
41
-
-
0034987571
-
Role of the serotonin transporter gene in the behavioral expression of autism
-
Tordjman S, Gutknecht L, Carlier M, Spitz E, Antoine C, Slama F, Carsalade V, Cohen DJ, Ferrari P, Roubertoux PL, Anderson GM. 2001. Role of the serotonin transporter gene in the behavioral expression of autism. Mol Psychiatry 6:434-439.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 434-439
-
-
Tordjman, S.1
Gutknecht, L.2
Carlier, M.3
Spitz, E.4
Antoine, C.5
Slama, F.6
Carsalade, V.7
Cohen, D.J.8
Ferrari, P.9
Roubertoux, P.L.10
Anderson, G.M.11
-
42
-
-
0037041326
-
Transmission disequilibrium studies of the serotonin 5-HT(2A) receptor gene (HTR2A) in autism
-
Veenstra-VanderWeele J, Kim SJ, Lord C, Courchesne R, Akshoomoff N, Leventhal BL, Courchesne E, Cook EH Jr. 2002. Transmission disequilibrium studies of the serotonin 5-HT(2A) receptor gene (HTR2A) in autism. Am J Med Genet 114:277-283.
-
(2002)
Am J Med Genet
, vol.114
, pp. 277-283
-
-
Veenstra-VanderWeele, J.1
Kim, S.J.2
Lord, C.3
Courchesne, R.4
Akshoomoff, N.5
Leventhal, B.L.6
Courchesne, E.7
Cook Jr., E.H.8
-
43
-
-
0031579427
-
Effects of neonatal serotonin depletion on the development of rat dentate granule cells
-
Yan W, Wilson CC, Haring JH. 1997. Effects of neonatal serotonin depletion on the development of rat dentate granule cells. Brain Res Dev Brain Res 98:177-184.
-
(1997)
Brain Res Dev Brain Res
, vol.98
, pp. 177-184
-
-
Yan, W.1
Wilson, C.C.2
Haring, J.H.3
-
44
-
-
0032904498
-
5-HTTLPR variants not associated with autistic spectrum disorders
-
Zhong N, Ye L, Ju W, Brown WT, Tsiouris J, Cohen I. 1999. 5-HTTLPR variants not associated with autistic spectrum disorders. Neurogenetics 2:129-131.
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(1999)
Neurogenetics
, vol.2
, pp. 129-131
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Zhong, N.1
Ye, L.2
Ju, W.3
Brown, W.T.4
Tsiouris, J.5
Cohen, I.6
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