-
1
-
-
0004235298
-
-
American Psychiatric Association:, ed 4. Washington, American Psychiatric Association
-
American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders DSM-IV, ed 4. Washington, American Psychiatric Association, 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders DSM-IV
-
-
-
2
-
-
0035958295
-
Pervasive developmental disorders in preschool children
-
Chakrabarti S, Fombonne E: Pervasive developmental disorders in preschool children. JAMA 2001;285:3093-3099.
-
(2001)
JAMA
, vol.285
, pp. 3093-3099
-
-
Chakrabarti, S.1
Fombonne, E.2
-
3
-
-
0036991144
-
The prevalence of autism spectrum disorders: Recent evidence and future challenges
-
Charman T: The prevalence of autism spectrum disorders: recent evidence and future challenges. Eur Child Adolesc Psychiatry 2002;11:249-256.
-
(2002)
Eur Child Adolesc Psychiatry
, vol.11
, pp. 249-256
-
-
Charman, T.1
-
4
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC: A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet 2003;73:886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.4
Spence, S.J.5
Palmer, A.A.6
Grunn, A.7
Juo, S.H.8
Terwilliger, J.D.9
Liu, J.10
Cantor, R.M.11
Geschwind, D.H.12
Gilliam, T.C.13
-
5
-
-
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: Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 1995;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
-
6
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein S, Rutter M: Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry 1997;18:297-321.
-
(1997)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
7
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M: A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 1989;30:405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
8
-
-
0029134874
-
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
-
Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH, Rutter M: Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet 1995;57:717-726.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
Rutter, M.7
-
9
-
-
0028857007
-
Polygenic disease: Methods for mapping complex disease traits
-
Weeks DE, Lathrop GM: Polygenic disease: methods for mapping complex disease traits. Trends Genet 1995;11:513-519.
-
(1995)
Trends Genet
, vol.11
, pp. 513-519
-
-
Weeks, D.E.1
Lathrop, G.M.2
-
10
-
-
0032454027
-
Chromosomal disorders and autism
-
Gillberg C: Chromosomal disorders and autism. J Autism Dev Disord 1998;28:415-425.
-
(1998)
J Autism Dev Disord
, vol.28
, pp. 415-425
-
-
Gillberg, C.1
-
11
-
-
4644315735
-
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
-
Bolton PF, Veltman MW, Weisblatt E, Holmes JR, Thomas NS, Youings SA, Thompson RJ, Roberts SE, Dennis NR, Browne CE, Goodsoon S, Moore V, Brown J: Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders. Psychiatr Genet 2004;14:131-137.
-
(2004)
Psychiatr Genet
, vol.14
, pp. 131-137
-
-
Bolton, P.F.1
Veltman, M.W.2
Weisblatt, E.3
Holmes, J.R.4
Thomas, N.S.5
Youings, S.A.6
Thompson, R.J.7
Roberts, S.E.8
Dennis, N.R.9
Browne, C.E.10
Goodsoon, S.11
Moore, V.12
Brown, J.13
-
12
-
-
0027476507
-
Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: An overview
-
Knoll JH, Wagstaff J, Lalande M: Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview. Am J Med Genet 1993;46:2-6.
-
(1993)
Am J Med Genet
, vol.46
, pp. 2-6
-
-
Knoll, J.H.1
Wagstaff, J.2
Lalande, M.3
-
13
-
-
0027026716
-
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
-
Ozcelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U: Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nat Genet 1992;2:265-269.
-
(1992)
Nat Genet
, vol.2
, pp. 265-269
-
-
Ozcelik, T.1
Leff, S.2
Robinson, W.3
Donlon, T.4
Lalande, M.5
Sanjines, E.6
Schinzel, A.7
Francke, U.8
-
14
-
-
0028206982
-
Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism
-
Arrieta I, Lobato MN, Martinez B, Criado B: Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism. Psychiatr Genet 1994;4:63-65.
-
(1994)
Psychiatr Genet
, vol.4
, pp. 63-65
-
-
Arrieta, I.1
Lobato, M.N.2
Martinez, B.3
Criado, B.4
-
15
-
-
13444260705
-
Autism and 15q11-q13 disorders: Behavioral, genetic, and pathophysiological issues
-
Dykens EM, Sutcliffe JS, Levitt P: Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues. Ment Retard Dev Disabil Res Rev 2004;10:284-291.
-
(2004)
Ment Retard Dev Disabil Res Rev
, vol.10
, pp. 284-291
-
-
Dykens, E.M.1
Sutcliffe, J.S.2
Levitt, P.3
-
16
-
-
14344252476
-
Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome
-
Graham JM, Rosner B, Dykens E, Visootsak J: Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome. Am J Med Genet 2005;133:240-247.
-
(2005)
Am J Med Genet
, vol.133
, pp. 240-247
-
-
Graham, J.M.1
Rosner, B.2
Dykens, E.3
Visootsak, J.4
-
17
-
-
0033590679
-
Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay
-
Mohandas TK, Park JP, Spellman RA, Filiano JJ, Mamourian AC, Hawk AB, Belloni DR, Noll WW, Moeschler JB: Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay. Am J Med Genet 1999;82:294-300.
-
(1999)
Am J Med Genet
, vol.82
, pp. 294-300
-
-
Mohandas, T.K.1
Park, J.P.2
Spellman, R.A.3
Filiano, J.J.4
Mamourian, A.C.5
Hawk, A.B.6
Belloni, D.R.7
Noll, W.W.8
Moeschler, J.B.9
-
18
-
-
0034088447
-
Genetic studies in autistic disorder and chromosome 15
-
Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER, Maddox LO, Vance JM, Abramson RK, Wright HH, Gilbert JR, Cuccaro ML, DeLong GR, Pericak-Vance MA: Genetic studies in autistic disorder and chromosome 15. Neurogenetics 2000;2:219-226.
-
(2000)
Neurogenetics
, vol.2
, pp. 219-226
-
-
Bass, M.P.1
Menold, M.M.2
Wolpert, C.M.3
Donnelly, S.L.4
Ravan, S.A.5
Hauser, E.R.6
Maddox, L.O.7
Vance, J.M.8
Abramson, R.K.9
Wright, H.H.10
Gilbert, J.R.11
Cuccaro, M.L.12
DeLong, G.R.13
Pericak-Vance, M.A.14
-
19
-
-
0032945941
-
The Paris Autism Research International Sibpair Study, genome-wide scan for autism susceptibility genes
-
Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Rastam M, Sponheim E, Coleman M, Zapella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M: The Paris Autism Research International Sibpair Study, genome-wide scan for autism susceptibility genes. Hum Mol Genet 1999;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
Zapella, M.8
Aschauer, H.9
Van Maldergem, L.10
Penet, C.11
Feingold, J.12
Brice, A.13
Leboyer, M.14
-
20
-
-
85047700330
-
Association between a GABRB3 polymorphism and autism
-
Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH, Fang Y, Song CY, Vitale R: Association between a GABRB3 polymorphism and autism. Mol Psychiatry 2002;7:311-316.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 311-316
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Greenberg, D.A.4
Kilifarski, M.5
Reichert, J.6
Cook, E.H.7
Fang, Y.8
Song, C.Y.9
Vitale, R.10
-
21
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
-
Cook EH, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E: Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Hum Genet 1998;62:1077-1083.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1077-1083
-
-
Cook, E.H.1
Courchesne, R.Y.2
Cox, N.J.3
Lord, C.4
Gonen, D.5
Guter, S.J.6
Lincoln, A.7
Nix, K.8
Haas, R.9
Leventhal, B.L.10
Courchesne, E.11
-
22
-
-
7644221741
-
A receptor subunit cluster and association to autism
-
A receptor subunit cluster and association to autism. Am J Med Genet 2004;131:51-59.
-
(2004)
Am J Med Genet
, vol.131
, pp. 51-59
-
-
McCauley, J.L.1
Olson, L.M.2
Delahanty, R.3
Amin, T.4
Nurmi, E.L.5
Organ, E.L.6
Jacobs, M.M.7
Folstein, S.E.8
Haines, J.L.9
Sutcliffe, J.S.10
-
23
-
-
18344386200
-
A receptor subunit genes in autistic disorder
-
A receptor subunit genes in autistic disorder. J Neurogenet 2001;15:245-259.
-
(2001)
J Neurogenet
, vol.15
, pp. 245-259
-
-
Menold, M.M.1
Shao, Y.2
Wolpert, C.M.3
Donnelly, S.L.4
Raiford, K.L.5
Martin, E.R.6
Ravan, S.A.7
Abramson, R.K.8
Wright, H.H.9
Delong, G.R.10
Cuccaro, M.L.11
Pericar-Vance, M.A.12
Gilbert, J.R.13
-
24
-
-
0003428096
-
-
Los Angeles, Western Psychological Services
-
Lord C, Rutter M, DiLavore P, Risi S: Autism Diagnostic Observation Schedule, Los Angeles, Western Psychological Services, 2002.
-
(2002)
Autism Diagnostic Observation Schedule
-
-
Lord, C.1
Rutter, M.2
DiLavore, P.3
Risi, S.4
-
27
-
-
33847283565
-
-
KEDI-WISC, ed 2. Seoul, Korean Educational Development Institute
-
Park KS, Yoon JR, Park HJ, Park HJ, Kwon KO: Korean Educational Developmental Institute - Wechsler Intelligence Scale for Children (KEDI-WISC), ed 2. Seoul, Korean Educational Development Institute, 2002.
-
(2002)
Korean Educational Developmental Institute - Wechsler Intelligence Scale for Children
-
-
Park, K.S.1
Yoon, J.R.2
Park, H.J.3
Park, H.J.4
Kwon, K.O.5
-
28
-
-
0242475326
-
LDA - a java-based linkage disequilibrium analyzer
-
Ding K, Zhou K, He F, Shen Y: LDA - a java-based linkage disequilibrium analyzer. Bioinformatics 2003;19:2147-2148.
-
(2003)
Bioinformatics
, vol.19
, pp. 2147-2148
-
-
Ding, K.1
Zhou, K.2
He, F.3
Shen, Y.4
-
29
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D: A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 1999;65:1170-1177.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
31
-
-
0033461783
-
Elevated levels of plasma and urine gamma-aminobutyric acid - a case study for an autistic child
-
Cohen BI: Elevated levels of plasma and urine gamma-aminobutyric acid - a case study for an autistic child. Autism 1999;3:437-440.
-
(1999)
Autism
, vol.3
, pp. 437-440
-
-
Cohen, B.I.1
-
33
-
-
0036691555
-
Elevated plasma gamma-aminobutyric acid (GABA) levels in autistic youngsters: Stimulus for a GABA hypothesis of autism
-
Dhossche D, Applegate H, Abraham A, Maertens P, Bland L, Bencsath A, Martinez J: Elevated plasma gamma-aminobutyric acid (GABA) levels in autistic youngsters: stimulus for a GABA hypothesis of autism. Med Sci Monit 2002;8:PR1-PR6.
-
(2002)
Med Sci Monit
, vol.8
-
-
Dhossche, D.1
Applegate, H.2
Abraham, A.3
Maertens, P.4
Bland, L.5
Bencsath, A.6
Martinez, J.7
-
34
-
-
0035755097
-
Density and distribution of hippocampal neurotransmitter receptors in autism: An autoradiographic study
-
Blatt GJ, Fitzgerald CM, Guptill JT, Booker AB, Kemper TL, Bauman ML: Density and distribution of hippocampal neurotransmitter receptors in autism: an autoradiographic study. J Autism Dev Disord 2001;31:537-543.
-
(2001)
J Autism Dev Disord
, vol.31
, pp. 537-543
-
-
Blatt, G.J.1
Fitzgerald, C.M.2
Guptill, J.T.3
Booker, A.B.4
Kemper, T.L.5
Bauman, M.L.6
-
35
-
-
0035026384
-
Postnatal maturation of human GABAA receptors measured with positron emission tomography
-
Chugani DC, Muzik O, Juhasz C, Janisse JJ, Ager J, Chugani HT: Postnatal maturation of human GABAA receptors measured with positron emission tomography. Ann Neurol 2001;49:618-626.
-
(2001)
Ann Neurol
, vol.49
, pp. 618-626
-
-
Chugani, D.C.1
Muzik, O.2
Juhasz, C.3
Janisse, J.J.4
Ager, J.5
Chugani, H.T.6
-
36
-
-
0029200592
-
A receptors and their structural determinants
-
A receptors and their structural determinants. Adv Biochem Psychopharmacol 1995;48: 1-16.
-
(1995)
Adv Biochem Psychopharmacol
, vol.48
, pp. 1-16
-
-
Barnard, E.A.1
-
37
-
-
0028977843
-
GABAA-receptor heterogeneity in the adult rat brain: Differential regional and cellular distribution of seven major subunits
-
Fritschy JM, Mohler H: GABAA-receptor heterogeneity in the adult rat brain: differential regional and cellular distribution of seven major subunits. J Comp Neurol 1995;359:154-194.
-
(1995)
J Comp Neurol
, vol.359
, pp. 154-194
-
-
Fritschy, J.M.1
Mohler, H.2
-
39
-
-
0032531430
-
Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome
-
DeLorey TM, Handforth A, Anagnostaras SG, Homanics GE, Minassian BA, Asatourian A, Fanselow MS, Delgado-Escueta A, Ellison GD, Olsen RW: Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. J Neurosci 1998;18: 8505-8514.
-
(1998)
J Neurosci
, vol.18
, pp. 8505-8514
-
-
DeLorey, T.M.1
Handforth, A.2
Anagnostaras, S.G.3
Homanics, G.E.4
Minassian, B.A.5
Asatourian, A.6
Fanselow, M.S.7
Delgado-Escueta, A.8
Ellison, G.D.9
Olsen, R.W.10
-
40
-
-
0032837062
-
GABA and epileptogenesis: Comparing gabrb3 gene-deficient mice with Angelman syndrome in man
-
DeLorey TM, Olsen RW: GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man. Epilepsy Res 1999;36:123-132.
-
(1999)
Epilepsy Res
, vol.36
, pp. 123-132
-
-
DeLorey, T.M.1
Olsen, R.W.2
-
41
-
-
12644290240
-
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
-
Homanics GE, DeLorey TM, Firestone LL, Quinlan JJ, Handforth A, Harrison NL, Krasowski MD, Rick CE, Korpi ER, Makela R, Brilliant MH, Hagiwara N, Ferguson C, Snyder K, Olsen RW: Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proc Natl Acad Sci USA 1997;94:4143-4148.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4143-4148
-
-
Homanics, G.E.1
DeLorey, T.M.2
Firestone, L.L.3
Quinlan, J.J.4
Handforth, A.5
Harrison, N.L.6
Krasowski, M.D.7
Rick, C.E.8
Korpi, E.R.9
Makela, R.10
Brilliant, M.H.11
Hagiwara, N.12
Ferguson, C.13
Snyder, K.14
Olsen, R.W.15
-
42
-
-
33746215247
-
-
ed 3. Hoboken, John Wiley & Sons
-
Volkmar FR, Paul R, Klin A, Cohen D: Handbook of Autism and Pervasive Developmental Disorders, ed 3. Hoboken, John Wiley & Sons, 2005.
-
(2005)
Handbook of Autism and Pervasive Developmental Disorders
-
-
Volkmar, F.R.1
Paul, R.2
Klin, A.3
Cohen, D.4
-
45
-
-
23644450062
-
The fears, phobias and anxieties of children with autism spectrum disorders and Down syndrome: Comparisons with developmentally and chronologically age matched children
-
Evans DW, Canavera K, Kleinpeter FL, Maccubbin E, Taga K: The fears, phobias and anxieties of children with autism spectrum disorders and Down syndrome: comparisons with developmentally and chronologically age matched children. Child Psychiatry Hum Dev 2005;36:3-26.
-
(2005)
Child Psychiatry Hum Dev
, vol.36
, pp. 3-26
-
-
Evans, D.W.1
Canavera, K.2
Kleinpeter, F.L.3
Maccubbin, E.4
Taga, K.5
-
46
-
-
0034892190
-
Anxiety in high-functioning children with autism
-
Gillott A, Furniss F, Walte A: Anxiety in high-functioning children with autism. Autism 2001;5:277-286.
-
(2001)
Autism
, vol.5
, pp. 277-286
-
-
Gillott, A.1
Furniss, F.2
Walte, A.3
-
47
-
-
0031829430
-
Comorbid anxiety symptoms in children with pervasive developmental disorders
-
Muris P, Steerneman P, Merckelbach H, Holdrinet I, Meesters C: Comorbid anxiety symptoms in children with pervasive developmental disorders. J Anxiety Disord 1998;12:387-393.
-
(1998)
J Anxiety Disord
, vol.12
, pp. 387-393
-
-
Muris, P.1
Steerneman, P.2
Merckelbach, H.3
Holdrinet, I.4
Meesters, C.5
-
48
-
-
0037499597
-
Psychiatric disorders in individuals with pervasive developmental disorder
-
Sverd J: Psychiatric disorders in individuals with pervasive developmental disorder. J Psychiatr Pract 2002;9:111-127.
-
(2002)
J Psychiatr Pract
, vol.9
, pp. 111-127
-
-
Sverd, J.1
-
49
-
-
0023605732
-
Paradoxical reactions elicited by diazepam in children with classic autism
-
Marrosu F, Marrosu G, Rachel MG, Biggio G: Paradoxical reactions elicited by diazepam in children with classic autism. Funct Neurol 1987;2:355-361.
-
(1987)
Funct Neurol
, vol.2
, pp. 355-361
-
-
Marrosu, F.1
Marrosu, G.2
Rachel, M.G.3
Biggio, G.4
-
50
-
-
0033569931
-
The International Molecular Genetic Study of Autism Consortium. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families
-
Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP: The International Molecular Genetic Study of Autism Consortium. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. Am J Med Genet 1999;88:492-496.
-
(1999)
Am J Med Genet
, vol.88
, pp. 492-496
-
-
Maestrini, E.1
Lai, C.2
Marlow, A.3
Matthews, N.4
Wallace, S.5
Bailey, A.6
Cook, E.H.7
Weeks, D.E.8
Monaco, A.P.9
-
51
-
-
0034615152
-
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
-
Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA: Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. Am J Med Genet 2000;96:43-48.
-
(2000)
Am J Med Genet
, vol.96
, pp. 43-48
-
-
Martin, E.R.1
Menold, M.M.2
Wolpert, C.M.3
Bass, M.P.4
Donnelly, S.L.5
Ravan, S.A.6
Zimmerman, A.7
Gilbert, J.R.8
Vance, J.M.9
Maddox, L.O.10
Wright, H.H.11
Abramson, R.K.12
DeLong, G.R.13
Cuccaro, M.L.14
Pericak-Vance, M.A.15
|