Genetics References Clinical studies Fra(X)(p22) not associated with infantile autism. Lancet 1984; 2

Download 0.6 Mb.
Date conversion29.03.2017
Size0.6 Mb.
  1   2   3   4   5   6   7   8   9   ...   12
Genetics References

Clinical studies

1. Fra(X)(p22) not associated with infantile autism. Lancet 1984; 2(8416): 1397.

2. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium. Hum Mol Genet 1998; 7(3): 571-578.
3. An autosomal genomic screen for autism. Am J Med Genet 2001; 105(8): 609-615.
4. Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet 2001; 105(8): 539-547.
5. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 2001; 69(3): 570-581.
6. Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Hum Mol Genet 2001; 10(9): 973-982.
7. Chromosome "hot spot" linked to autism. Harv Ment Health Lett 2008; 24(11): 7.

8. Special report: aCGH for the genetic evaluation of patients with developmental delay/mental retardation or autism spectrum disorder. Technol Eval Cent Asses Program Exec Summ 2009; 23(10): 1-5.

9. Abdul-Rahman OA, Hudgins L. The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders. Genet Med 2006; 8(1): 50-54.
10. Abramson RK, Wright HH. Autism: the difficult hunt for disease genes. J S C Med Assoc 2006; 102(8): 277-279.
11. Abu-Amero KK, Hellani AM, Salih MA, Seidahmed MZ, Elmalik TS, Zidan G et al. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation. BMC Med Genet 2010; 11: 135.
12. Abu-Elneel K, Liu T, Gazzaniga FS, Nishimura Y, Wall DP, Geschwind DH et al. Heterogeneous dysregulation of microRNAs across the autism spectrum. Neurogenetics 2008; 9(3): 153-161.
13. Adams M, Lucock M, Stuart J, Fardell S, Baker K, Ng X. Preliminary evidence for involvement of the folate gene polymorphism 19bp deletion-DHFR in occurrence of autism. Neurosci Lett 2007; 422(1): 24-29.
14. Addington AM, Gauthier J, Piton A, Hamdan FF, Raymond A, Gogtay N et al. A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders. Mol Psychiatry 2010.

15. Adegbola A, Gao H, Sommer S, Browning M. A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD). Am J Med Genet A 2008; 146A(4): 505-511.

16. Akbarian S. Clinical experts on Rett disorder. Pediatr Rehabil 2002; 5(2): 117-118.
17. Alarcon M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet 2008; 82(1): 150-159.
18. Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet 2002; 70(1): 60-71.
19. Alarcon M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH. Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Mol Psychiatry 2005; 10(8): 747-757.
20. Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H. A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Autism Res 2010; 3(2): 47-52.
21. Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M et al. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry 2009; 14(6): 590-600.

22. Alpert M. The autism diet. Sci Am 2007; 296(4): 19-20.

23. Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA et al. Association of common variants in the Joubert syndrome gene (AHI1) with autism. Hum Mol Genet 2008; 17(24): 3887-3896.
24. Aman MG. Treatment planning for patients with autism spectrum disorders. J Clin Psychiatry 2005; 66 Suppl 10: 38-45.
25. Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK et al. Examination of association of genes in the serotonin system to autism. Neurogenetics 2009; 10(3): 209-216.
26. Anderson GM. Genetics of childhood disorders: XLV. Autism, part 4: serotonin in autism. J Am Acad Child Adolesc Psychiatry 2002; 41(12): 1513-1516.
27. Anderson GM, Gutknecht L, Cohen DJ, Brailly-Tabard S, Cohen JH, Ferrari P et al. Serotonin transporter promoter variants in autism: functional effects and relationship to platelet hyperserotonemia. Mol Psychiatry 2002; 7(8): 831-836.
28. Anitha A, Nakamura K, Yamada K, Suda S, Thanseem I, Tsujii M et al. Genetic analyses of roundabout (ROBO) axon guidance receptors in autism. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(7): 1019-1027.

29. Anneren G, Dahl N, Uddenfeldt U, Janols LO. Asperger syndrome in a boy with a balanced de novo translocation: t(17;19)(p13.3;p11). Am J Med Genet 1995; 56(3): 330-331.

30. Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR et al. A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 2010; 19(20): 4072-4082.
31. Antshel KM, Aneja A, Strunge L, Peebles J, Fremont WP, Stallone K et al. Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion). J Autism Dev Disord 2007; 37(9): 1776-1786.
32. Anvret M, Gillberg C, Wahlstrom J, Albertsson-Wikland K, Davies K. Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family. Clin Genet 1988; 34(4): 265-271.
33. Arieff Z, Kaur M, Gameeldien H, van der Merwe L, Bajic VB. 5-HTTLPR polymorphism: analysis in South African autistic individuals. Hum Biol 2010; 82(3): 291-300.
34. Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet 2008; 82(1): 160-164.
35. Armstrong DD. Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain? Brain Dev 2005; 27 Suppl 1: S72-S76.

36. Armstrong DD, Deguchi K, Antallfy B. Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain. J Child Neurol 2003; 18(10): 683-687.

37. Armstrong J, Aibar E, Pineda M, Perez MM, Gean E, Carrera M et al. Prenatal diagnosis in Rett syndrome. Fetal Diagn Ther 2002; 17(4): 200-204.
38. 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(1): 63-65.
39. Arrieta I, Nunez T, Martinez B, Perez A, Telez M, Criado B et al. Chromosomal fragility in a behavioral disorder. Behav Genet 2002; 32(6): 397-412.
40. Aschner M, Ceccatelli S. Are neuropathological conditions relevant to ethylmercury exposure? Neurotox Res 2010; 18(1): 59-68.
41. Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL et al. Genetic studies of autistic disorder and chromosome 7. Genomics 1999; 61(3): 227-236.
42. Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA et al. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatr Genet 2007; 17(4): 221-226.

43. Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM et al. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Ann Hum Genet 2006; 70(Pt 3): 281-292.

44. Assumpcao F, Santos RC, Rosario M, Mercadante M. Brief report: autism and Aarskog syndrome. J Autism Dev Disord 1999; 29(2): 179-181.
45. Assumpcao Junior FB. Brief report: a case of chromosome 22 alteration associated with autistic syndrome. J Autism Dev Disord 1998; 28(3): 253-256.
46. Atladottir HO, Pedersen MG, Thorsen P, Mortensen PB, Deleuran B, Eaton WW et al. Association of family history of autoimmune diseases and autism spectrum disorders. Pediatrics 2009; 124(2): 687-694.
47. August GJ. A genetic marker associated with infantile autism. Am J Psychiatry 1983; 140(6): 813.
48. Auranen M, Nieminen T, Majuri S, Vanhala R, Peltonen L, Jarvela I. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families. Mol Psychiatry 2000; 5(3): 320-322.
49. Auranen M, Vanhala R, Jarvela I. [First gene connected to autism spectrum disorders has been found]. Duodecim 2000; 116(20): 2185-2187.

50. Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T et al. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet 2002; 71(4): 777-790.

51. Auranen M, Varilo T, Alen R, Vanhala R, Ayers K, Kempas E et al. Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland. Mol Psychiatry 2003; 8(10): 879-884.
52. Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR et al. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. Am J Hum Genet 2010; 87(3): 316-324.
53. Azzoni A, Raja M. [A case of pervasive developmental disorder with chromosomal translocation (X; 4) (p11; q13)]. Encephale 2006; 32(3 Pt 1): 325-327.
54. Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL. Copy number and sequence variants implicate APBA2 as an autism candidate gene. Autism Res 2009; 2(6): 359-364.
55. Bacchelli E, Blasi F, Biondolillo M, Lamb JA, Bonora E, Barnby G et al. Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Mol Psychiatry 2003; 8(11): 916-924.

56. Badner JA, Gershon ES. Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7. Mol Psychiatry 2002; 7(1): 56-66.

57. Bailey A, Bolton P, Butler L, Le Couteur A, Murphy M, Scott S et al. Prevalence of the fragile X anomaly amongst autistic twins and singletons. J Child Psychol Psychiatry 1993; 34(5): 673-688.
58. Bailey A, Parr J. Implications of the broader phenotype for concepts of autism. Novartis Found Symp 2003; 251: 26-35; discussion 36-47, 109-111, 281-197.
59. Bakare MO, Ikegwuonu NN. Childhood autism in a 13 year old boy with oculocutaneous albinism: a case report. J Med Case Reports 2008; 2: 56.
60. Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet 2008; 82(1): 165-173.
61. Barbosa-Goncalves A, Vendrame-Goloni CB, Martins AL, Fett-Conte AC. Subtelomeric region of chromosome 2 in patients with autism spectrum disorders. Genet Mol Res 2008; 7(2): 527-533.
62. Barnby G, Abbott A, Sykes N, Morris A, Weeks DE, Mott R et al. Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. Am J Hum Genet 2005; 76(6): 950-966.

63. Baron CA, Tepper CG, Liu SY, Davis RR, Wang NJ, Schanen NC et al. Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes. Hum Mol Genet 2006; 15(6): 853-869.

64. Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL et al. An autosomal genomic screen for autism. Collaborative linkage study of autism. Am J Med Genet 1999; 88(6): 609-615.
65. Bartlett CW, Goedken R, Vieland VJ. Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set. Am J Hum Genet 2005; 76(4): 688-695.
66. Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER et al. Genetic studies in autistic disorder and chromosome 15. Neurogenetics 2000; 2(4): 219-226.
67. Battaglia A, Bonaglia MC. The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders. Am J Med Genet C Semin Med Genet 2006; 142C(1): 8-12.
68. Battaglia A, Carey JC. Etiologic yield of autistic spectrum disorders: a prospective study. Am J Med Genet C Semin Med Genet 2006; 142C(1): 3-7.
69. Bayou N, Belhadj A, Daoud H, Briault S, Helayem MB, Chaabouni H et al. Exploring the 7p22.1 chromosome as a candidate region for autism. J Biomed Biotechnol 2010; 2010: 423894.

70. Bayou N, M'Rad R, Belhaj A, Daoud H, Ben Jemaa L, Zemni R et al. De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder. J Biomed Biotechnol 2008; 2008: 231904.

71. Becker KG, Schultz ST. Similarities in features of autism and asthma and a possible link to acetaminophen use. Med Hypotheses 2010; 74(1): 7-11.
72. Bedogni F, Hodge RD, Nelson BR, Frederick EA, Shiba N, Daza RA et al. Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology. Gene Expr Patterns 2010; 10(1): 9-15.
73. Behjati F, Shafaghati Y, Firouzabadi SG, Kahrizi K, Bagherizadeh I, Najmabadi H et al. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism. Eur J Med Genet 2008; 51(6): 608-614.
74. Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM et al. Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2. Biol Psychiatry 2009; 66(10): 911-917.
75. Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S et al. Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. Am J Hum Genet 2005; 77(5): 851-868.
76. Benezech M, Noel B. Fra (X) syndrome and autism. Clin Genet 1985; 28(1): 93.

77. Benezech M, Noel B, Noel L, Bourgeois M. [Fragile X chromosome and autistic mental retardation. Apropos of 23 cases]. Ann Med Psychol (Paris) 1983; 141(9): 1006-1011.

78. Ben-Shachar S, Lanpher B, German JR, Qasaymeh M, Potocki L, Nagamani SC et al. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders. J Med Genet 2009; 46(6): 382-388.
79. Berg JS, Brunetti-Pierri N, Peters SU, Kang SH, Fong CT, Salamone J et al. Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region. Genet Med 2007; 9(7): 427-441.
80. Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U et al. Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nat Genet 2010; 42(6): 489-491.
81. Betancur C, Corbex M, Spielewoy C, Philippe A, Laplanche JL, Launay JM et al. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Mol Psychiatry 2002; 7(1): 67-71.
82. Beyer KS, Blasi F, Bacchelli E, Klauck SM, Maestrini E, Poustka A. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism. Hum Genet 2002; 111(4-5): 305-309.

83. Beyer KS, Klauck SM, Benner A, Poustka F, Poustka A. Association studies of the HOPA dodecamer duplication variant in different subtypes of autism. Am J Med Genet 2002; 114(1): 110-115.

84. Beyer KS, Klauck SM, Wiemann S, Poustka A. Construction of a physical map of an autism susceptibility region in 7q32.3-q33. Gene 2001; 272(1-2): 85-91.
85. Bhat SS, Ladd S, Grass F, Spence JE, Brasington CK, Simensen RJ et al. Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism. Clin Genet 2008; 73(1): 94-96.
86. Blackman JA, Selzer SC, Patil S, Van Dyke DC. Autistic disorder associated with an iso-dicentric Y chromosome. Dev Med Child Neurol 1991; 33(2): 162-166.
87. Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ et al. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. Eur J Hum Genet 2006; 14(1): 123-126.
88. Blasi F, Bacchelli E, Pesaresi G, Carone S, Bailey AJ, Maestrini E. Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection. Am J Med Genet B Neuropsychiatr Genet 2006; 141B(3): 220-221.

89. Blomquist HK, Bohman M, Edvinsson SO, Gillberg C, Gustavson KH, Holmgren G et al. Frequency of the fragile X syndrome in infantile autism. A Swedish multicenter study. Clin Genet 1985; 27(2): 113-117.

90. Blondis TA, Cook E, Jr., Koza-Taylor P, Finn T. Asperger syndrome associated with Steinert's myotonic dystrophy. Dev Med Child Neurol 1996; 38(9): 840-847.
91. Boccone L, Dessi V, Zappu A, Piga S, Piludu MB, Rais M et al. Bannayan-Riley-Ruvalcaba syndrome with reactive nodular lymphoid hyperplasia and autism and a PTEN mutation. Am J Med Genet A 2006; 140(18): 1965-1969.
92. Bolton P, Macdonald H, Pickles A, Rios P, Goode S, Crowson M et al. A case-control family history study of autism. J Child Psychol Psychiatry 1994; 35(5): 877-900.
93. Bolton P, Powell J, Rutter M, Buckle V, Yates JR, Ishikawa-Brush Y et al. Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1). Psychiatr Genet 1995; 5(2): 51-55.
94. Bolton P, Rutter M, Butler L, Summers D. Females with autism and the fragile X. J Autism Dev Disord 1989; 19(3): 473-476.
95. Bolton PF. Neuroepileptic correlates of autistic symptomatology in tuberous sclerosis. Ment Retard Dev Disabil Res Rev 2004; 10(2): 126-131.

96. Bolton PF, Griffiths PD. Association of tuberous sclerosis of temporal lobes with autism and atypical autism. Lancet 1997; 349(9049): 392-395.

97. Bolton PF, Veltman MW, Weisblatt E, Holmes JR, Thomas NS, Youings SA et al. Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders. Psychiatr Genet 2004; 14(3): 131-137.
98. Bonati MT, Finelli P, Giardino D, Gottardi G, Roberts W, Larizza L. Trisomy 15q25.2-qter in an autistic child: genotype-phenotype correlations. Am J Med Genet A 2005; 133A(2): 184-188.
99. Bonnet C, Gregoire MJ, Brochet K, Raffo E, Leheup B, Jonveaux P. Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization. J Hum Genet 2006; 51(9): 815-821.
100. Bonora E, Bacchelli E, Levy ER, Blasi F, Marlow A, Monaco AP et al. Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. Mol Psychiatry 2002; 7(3): 289-301.
101. Bonora E, Beyer KS, Lamb JA, Parr JR, Klauck SM, Benner A et al. Analysis of reelin as a candidate gene for autism. Mol Psychiatry 2003; 8(10): 885-892.

102. Bonora E, Lamb JA, Barnby G, Sykes N, Moberly T, Beyer KS et al. Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. Eur J Hum Genet 2005; 13(2): 198-207.

103. Borg I, Squire M, Menzel C, Stout K, Morgan D, Willatt L et al. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation. J Med Genet 2002; 39(6): 391-399.
104. Borgatti R, Piccinelli P, Passoni D, Raggi E, Ferrarese C. Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15. J Child Neurol 2001; 16(12): 911-914.
105. Bottini N, De Luca D, Saccucci P, Fiumara A, Elia M, Porfirio MC et al. Autism: evidence of association with adenosine deaminase genetic polymorphism. Neurogenetics 2001; 3(2): 111-113.
106. Bozdagi O, Sakurai T, Papapetrou D, Wang X, Dickstein DL, Takahashi N et al. Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Mol Autism 2010; 1(1): 15.
107. Brandau DT, Lund M, Cooley LD, Sanger WG, Butler MG. Autistic and dysmorphic features associated with a submicroscopic 2q33.3-q34 interstitial deletion detected by array comparative genomic hybridization. Am J Med Genet A 2008; 146A(4): 521-524.

108. Braun NN, Reutiman TJ, Lee S, Folsom TD, Fatemi SH. Expression of phosphodiesterase 4 is altered in the brains of subjects with autism. Neuroreport 2007; 18(17): 1841-1844.

109. Bremer A, Giacobini M, Nordenskjold M, Brondum-Nielsen K, Mansouri M, Dahl N et al. Screening for copy number alterations in loci associated with autism spectrum disorders by two-color multiplex ligation-dependent probe amplification. Am J Med Genet B Neuropsychiatr Genet 2010; 153B(1): 280-285.
110. Brown WT, Friedman E, Jenkins EC, Brooks J, Wisniewski K, Raguthu S et al. Association of fragile X syndrome with autism. Lancet 1982; 1(8263): 100.
111. Brown WT, Jenkins EC, Cohen IL, Fisch GS, Wolf-Schein EG, Gross A et al. Fragile X and autism: a multicenter survey. Am J Med Genet 1986; 23(1-2): 341-352.
112. Brown WT, Jenkins EC, Friedman E, Brooks J, Wisniewski K, Raguthu S et al. Autism is associated with the fragile-X syndrome. J Autism Dev Disord 1982; 12(3): 303-308.
113. Bruining H, de Sonneville L, Swaab H, de Jonge M, Kas M, van Engeland H et al. Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes. PLoS One 2010; 5(5): e10887.

114. Brune CW, Kim SJ, Hanna GL, Courchesne E, Lord C, Leventhal BL et al. Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample. Autism Res 2008;

  1   2   3   4   5   6   7   8   9   ...   12

The database is protected by copyright © 2017
send message

    Main page