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

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217. Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC et al. Pax6 3' deletion results in aniridia, autism and mental retardation. Hum Genet 2008; 123(4): 371-378.
218. Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC et al. Novel copy number variants in children with autism and additional developmental anomalies. J Neurodev Disord 2009; 1(4): 292-301.
219. De Braekeleer M, Tremblay M, Thivierge J. Genetic analysis of genealogies in mentally retarded autistic probands from Saguenay Lac-Saint-Jean (Quebec, Canada). Ann Genet 1996; 39(1): 47-50.
220. de Bruijn DR, van Dijk AH, Pfundt R, Hoischen A, Merkx GF, Gradek GA et al. Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression. Mol Syndromol 2010; 1(1): 46-57.
221. de Krom M, Staal WG, Ophoff RA, Hendriks J, Buitelaar J, Franke B et al. A common variant in DRD3 receptor is associated with autism spectrum disorder. Biol Psychiatry 2009; 65(7): 625-630.

222. de la Barra F, Skoknic V, Alliende A, Raimann E, Cortes F, Lacassie Y. [Twins with autism and mental retardation associated with balanced (7;20) chromosomal translocation]. Rev Chil Pediatr 1986; 57(6): 549-554.

223. Della Monica M, Lonardo F, Faravelli F, Pierluigi M, Luquetti DV, De Gregori M et al. A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q. Am J Med Genet A 2007; 143A(22): 2733-2737.
224. DeLong R. Autism and familial major mood disorder: are they related? J Neuropsychiatry Clin Neurosci 2004; 16(2): 199-213.
225. Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R et al. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders. Biol Psychiatry 2009; 66(4): 349-359.
226. Derwinska K, Bernaciak J, Wisniowiecka-Kowalnik B, Obersztyn E, Bocian E, Stankiewicz P. Autistic features with speech delay in a girl with an approximately 1.5-Mb deletion in 6q16.1, including GPR63 and FUT9. Clin Genet 2009; 75(2): 199-202.
227. Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P et al. Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. Am J Med Genet A 2010; 152A(9): 2346-2354.

228. Devlin B, Bennett P, Cook EH, Jr., Dawson G, Gonen D, Grigorenko EL et al. No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network. Am J Med Genet 2002; 114(6): 667-672.

229. Devlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W et al. Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network. Am J Med Genet B Neuropsychiatr Genet 2004; 126B(1): 46-50.
230. Di Bella MA, Cali F, Seidita G, Mirisola M, Ragusa A, Ragalmuto A et al. Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation. Am J Med Genet B Neuropsychiatr Genet 2006; 141B(6): 584-590.
231. Dimitropoulos A, Schultz RT. Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings. Curr Psychiatry Rep 2007; 9(2): 159-164.
232. Dissanayake C, Bui Q, Bulhak-Paterson D, Huggins R, Loesch DZ. Behavioural and cognitive phenotypes in idiopathic autism versus autism associated with fragile X syndrome. J Child Psychol Psychiatry 2009; 50(3): 290-299.
233. Donnelly SL, Wolpert CM, Menold MM, Bass MP, Gilbert JR, Cuccaro ML et al. Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome. Am J Med Genet 2000; 96(3): 312-316.

234. dos Santos PA, Longo D, Brandalize AP, Schuler-Faccini L. MTHFR C677T is not a risk factor for autism spectrum disorders in South Brazil. Psychiatr Genet 2010; 20(4): 187-189.

235. Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet 2007; 39(1): 25-27.
236. Dutta S, Das S, Guhathakurta S, Sen B, Sinha S, Chatterjee A et al. Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder. Cell Mol Neurobiol 2007; 27(8): 1035-1047.
237. Dutta S, Guhathakurta S, Sinha S, Chatterjee A, Ahmed S, Ghosh S et al. Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism. Am J Med Genet B Neuropsychiatr Genet 2007; 144B(1): 106-112.
238. Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. Neurosci Lett 2008; 441(1): 56-60.

239. Dykens EM, Sutcliffe JS, Levitt P. Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues. Ment Retard Dev Disabil Res Rev 2004; 10(4): 284-291.

240. Eagleson KL, Gravielle MC, Schlueter McFadyen-Ketchum LJ, Russek SJ, Farb DH, Levitt P. Genetic disruption of the autism spectrum disorder risk gene PLAUR induces GABAA receptor subunit changes. Neuroscience 2010; 168(3): 797-810.
241. Edelmann L, Prosnitz A, Pardo S, Bhatt J, Cohen N, Lauriat T et al. An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism. J Med Genet 2007; 44(2): 136-143.
242. Eichler EE, Zimmerman AW. A hot spot of genetic instability in autism. N Engl J Med 2008; 358(7): 737-739.
243. Ekstrom AB, Hakenas-Plate L, Samuelsson L, Tulinius M, Wentz E. Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(6): 918-926.
244. Eliez S. Autism in children with 22q11.2 deletion syndrome. J Am Acad Child Adolesc Psychiatry 2007; 46(4): 433-434; author reply 434-434.

245. Endo T, Kitamura H, Tamura R, Egawa J, Sugai T, Fukui N et al. 5-HTTLPR polymorphism influences prefrontal neurochemical metabolites in autism spectrum disorder. Psychiatry Res 2010; 183(2): 170-173.

246. Enstrom AM, Lit L, Onore CE, Gregg JP, Hansen RL, Pessah IN et al. Altered gene expression and function of peripheral blood natural killer cells in children with autism. Brain Behav Immun 2009; 23(1): 124-133.
247. Erturk O, Bilguvar K, Korkmaz B, Bayri Y, Bayrakli F, Arlier Z et al. A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin. Am J Med Genet A 2010; 152A(4): 1039-1042.
248. Eskenazi B, Huen K, Marks A, Harley KG, Bradman A, Barr DB et al. PON1 and neurodevelopment in children from the CHAMACOS study exposed to organophosphate pesticides in utero. Environ Health Perspect 2010; 118(12): 1775-1781.
249. Estecio M, Fett-Conte AC, Varella-Garcia M, Fridman C, Silva AE. Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders. J Autism Dev Disord 2002; 32(1): 35-41.
250. Ezugha H, Goldenthal M, Valencia I, Anderson CE, Legido A, Marks H. 5q14.3 deletion manifesting as mitochondrial disease and autism: case report. J Child Neurol 2010; 25(10): 1232-1235.

251. Fatemi SH, Snow AV, Stary JM, Araghi-Niknam M, Reutiman TJ, Lee S et al. Reelin signaling is impaired in autism. Biol Psychiatry 2005; 57(7): 777-787.

252. Fatemi SH, Stary JM, Halt AR, Realmuto GR. Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum. J Autism Dev Disord 2001; 31(6): 529-535.
253. Felder B, Radlwimmer B, Benner A, Mincheva A, Todt G, Beyer KS et al. FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. Am J Med Genet A 2009; 149A(5): 952-959.
254. Feng J, Schroer R, Yan J, Song W, Yang C, Bockholt A et al. High frequency of neurexin 1beta signal peptide structural variants in patients with autism. Neurosci Lett 2006; 409(1): 10-13.
255. Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P et al. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder. J Med Genet 2010; 47(3): 195-203.
256. Ferrante P, Saresella M, Guerini FR, Marzorati M, Musetti MC, Cazzullo AG. Significant association of HLA A2-DR11 with CD4 naive decrease in autistic children. Biomed Pharmacother 2003; 57(8): 372-374.

257. Filipek PA, Juranek J, Smith M, Mays LZ, Ramos ER, Bocian M et al. Mitochondrial dysfunction in autistic patients with 15q inverted duplication. Ann Neurol 2003; 53(6): 801-804.

258. Fine SE, Weissman A, Gerdes M, Pinto-Martin J, Zackai EH, McDonald-McGinn DM et al. Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome. J Autism Dev Disord 2005; 35(4): 461-470.
259. Finelli P, Natacci F, Bonati MT, Gottardi G, Engelen JJ, de Die-Smulders CE et al. FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour. J Med Genet 2004; 41(7): e90.
260. Flax JF, Hare A, Azaro MA, Vieland VJ, Brzustowicz LM. Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci. J Neurodev Disord 2010; 2(4): 210-223.
261. Flejter WL, Bennett-Baker PE, Ghaziuddin M, McDonald M, Sheldon S, Gorski JL. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. Am J Med Genet 1996; 61(2): 182-187.

262. Floris C, Rassu S, Boccone L, Gasperini D, Cao A, Crisponi L. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area. Eur J Hum Genet 2008; 16(6): 696-704.

263. Folstein S, Rutter M. Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry 1977; 18(4): 297-321.
264. Fon EA, Sarrazin J, Meunier C, Alarcia J, Shevell MI, Philippe A et al. Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutation. Am J Med Genet 1995; 60(6): 554-557.
265. Fontenelle LF, Mendlowicz MV, Bezerra de Menezes G, dos Santos Martins RR, Versiani M. Asperger Syndrome, obsessive-compulsive disorder, and major depression in a patient with 45,X/46,XY mosaicism. Psychopathology 2004; 37(3): 105-109.
266. Francke U. Discovery of the Rett syndrome gene and its function. Turk J Pediatr 2000; 42(4): 271.
267. Freitag CM, Agelopoulos K, Huy E, Rothermundt M, Krakowitzky P, Meyer J et al. Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder. Eur Child Adolesc Psychiatry 2010; 19(1): 67-74.
268. Fryns JP, Kleczkowska A. Autism and ring chromosome 18 mosaicism. Clin Genet 1992; 42(1): 55.

269. Fujita E, Dai H, Tanabe Y, Zhiling Y, Yamagata T, Miyakawa T et al. Autism spectrum disorder is related to endoplasmic reticulum stress induced by mutations in the synaptic cell adhesion molecule, CADM1. Cell Death Dis 2010; 1: e47.

270. Gadow KD, Devincent CJ, Olvet DM, Pisarevskaya V, Hatchwell E. Association of DRD4 polymorphism with severity of oppositional defiant disorder, separation anxiety disorder and repetitive behaviors in children with autism spectrum disorder. Eur J Neurosci 2010; 32(6): 1058-1065.
271. Gadow KD, DeVincent CJ, Pisarevskaya V, Olvet DM, Xu W, Mendell NR et al. Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorder. Prog Neuropsychopharmacol Biol Psychiatry 2010; 34(7): 1208-1214.
272. Gadow KD, Roohi J, DeVincent CJ, Hatchwell E. Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder. J Child Psychol Psychiatry 2008; 49(12): 1331-1338.
273. Gadow KD, Roohi J, DeVincent CJ, Kirsch S, Hatchwell E. Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder. J Autism Dev Disord 2009; 39(11): 1542-1551.

274. Gadow KD, Roohi J, DeVincent CJ, Kirsch S, Hatchwell E. Glutamate transporter gene (SLC1A1) single nucleotide polymorphism (rs301430) and repetitive behaviors and anxiety in children with autism spectrum disorder. J Autism Dev Disord 2010; 40(9): 1139-1145.

275. Gaita L, Manzi B, Sacco R, Lintas C, Altieri L, Lombardi F et al. Decreased serum arylesterase activity in autism spectrum disorders. Psychiatry Res 2010; 180(2-3): 105-113.
276. Galasso C, Lo-Castro A, Lalli C, Nardone AM, Gullotta F, Curatolo P. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism. J Child Neurol 2008; 23(7): 802-806.
277. Gallagher L, Becker K, Kearney G, Dunlop A, Stallings R, Green A et al. Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3). J Autism Dev Disord 2003; 33(1): 105-108.
278. Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M. No association between allelic variants of HOXA1/HOXB1 and autism. Am J Med Genet B Neuropsychiatr Genet 2004; 124B(1): 64-67.
279. Gans DJ. Additional evidence for genetic component in autism. J Autism Dev Disord 1989; 19(1): 175-176.
280. Garbett K, Ebert PJ, Mitchell A, Lintas C, Manzi B, Mirnics K et al. Immune transcriptome alterations in the temporal cortex of subjects with autism. Neurobiol Dis 2008; 30(3): 303-311.

281. Gauthier J, Bonnel A, St-Onge J, Karemera L, Laurent S, Mottron L et al. NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. Am J Med Genet B Neuropsychiatr Genet 2005; 132B(1): 74-75.

282. Gauthier J, Joober R, Dube MP, St-Onge J, Bonnel A, Gariepy D et al. Autism spectrum disorders associated with X chromosome markers in French-Canadian males. Mol Psychiatry 2006; 11(2): 206-213.
283. Gauthier J, Joober R, Mottron L, Laurent S, Fuchs M, De Kimpe V et al. Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. Am J Med Genet A 2003; 118A(2): 172-175.
284. Gauthier J, Spiegelman D, Piton A, Lafreniere RG, Laurent S, St-Onge J et al. Novel de novo SHANK3 mutation in autistic patients. Am J Med Genet B Neuropsychiatr Genet 2009; 150B(3): 421-424.
285. Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH. Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder. Mol Psychiatry 2004; 9(5): 474-484.
286. Ghaziuddin M. Autism in Down's syndrome: a family history study. J Intellect Disabil Res 2000; 44 ( Pt 5): 562-566.
287. Ghaziuddin M, Burmeister M. Deletion of chromosome 2q37 and autism: a distinct subtype? J Autism Dev Disord 1999; 29(3): 259-263.

288. Ghaziuddin M, Sheldon S, Tsai LY, Alessi N. Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder. J Intellect Disabil Res 1993; 37 ( Pt 3): 313-317.

289. Giannandrea M, Bianchi V, Mignogna ML, Sirri A, Carrabino S, D'Elia E et al. Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly. Am J Hum Genet 2010; 86(2): 185-195.
290. Gillberg C. Identical triplets with infantile autism and the fragile-X syndrome. Br J Psychiatry 1983; 143: 256-260.
291. Gillberg C, Cederlund M. Asperger syndrome: familial and pre- and perinatal factors. J Autism Dev Disord 2005; 35(2): 159-166.
292. Gillberg C, Ohlson VA, Wahlstrom J, Steffenburg S, Blix K. Monozygotic female twins with autism and the fragile-X syndrome (AFRAX). J Child Psychol Psychiatry 1988; 29(4): 447-451.
293. Gillberg C, Persson E, Wahlstrom J. The autism-fragile-X syndrome (AFRAX): a population-based study of ten boys. J Ment Defic Res 1986; 30 ( Pt 1): 27-39.
294. Gillberg C, Steffenburg S, Wahlstrom J, Gillberg IC, Sjostedt A, Martinsson T et al. Autism associated with marker chromosome. J Am Acad Child Adolesc Psychiatry 1991; 30(3): 489-494.

295. Gillberg C, Wahlstrom J. Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases. Dev Med Child Neurol 1985; 27(3): 293-304.

296. Gillberg C, Wahlstrom J, Hagberg B. Infantile autism and Rett's syndrome: common chromosomal denominator. Lancet 1984; 2(8411): 1094-1095.
297. Gillberg C, Winnergard I, Wahlstrom J. The sex chromosomes--one key to autism? An XYY case of infantile autism. Appl Res Ment Retard 1984; 5(3): 353-360.
298. Gilling M, Lauritsen MB, Moller M, Henriksen KF, Vicente A, Oliveira G et al. A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. Eur J Hum Genet 2008; 16(3): 312-319.
299. Giunco CT, de Oliveira AB, Carvalho-Salles AB, Souza DS, Silva AE, da Rocha SS et al. Association between APOE polymorphisms and predisposition for autism. Psychiatr Genet 2009; 19(6): 338.
300. Giunco CT, Moretti-Ferreira D, Silva AE, Rocha SS, Fett-Conte AC. MOMO syndrome associated with autism: a case report. Genet Mol Res 2008; 7(4): 1223-1225.
301. Glancy M, Barnicoat A, Vijeratnam R, de Souza S, Gilmore J, Huang S et al. Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties. Eur J Hum Genet 2009; 17(1): 37-43.

302. Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009; 459(7246): 569-573.

303. Goffin A, Hoefsloot LH, Bosgoed E, Swillen A, Fryns JP. PTEN mutation in a family with Cowden syndrome and autism. Am J Med Genet 2001; 105(6): 521-524.
304. Goin-Kochel RP, Abbacchi A, Constantino JN. Lack of evidence for increased genetic loading for autism among families of affected females: a replication from family history data in two large samples. Autism 2007; 11(3): 279-286.
305. Goin-Kochel RP, Porter AE, Peters SU, Shinawi M, Sahoo T, Beaudet AL. The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations. Autism Res 2009; 2(2): 98-108.
306. Goizet C, Excoffier E, Taine L, Taupiac E, El Moneim AA, Arveiler B et al. Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH. Am J Med Genet 2000; 96(6): 839-844.
307. Goldfine PE, McPherson PM, Heath GA, Hardesty VA, Beauregard LJ, Gordon B. Association of fragile X syndrome with autism. Am J Psychiatry 1985; 142(1): 108-110.

308. Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P et al. Analysis of X chromosome inactivation in autism spectrum disorders. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(6): 830-835.

309. Gong X, Delorme R, Fauchereau F, Durand CM, Chaste P, Betancur C et al. An investigation of ribosomal protein L10 gene in autism spectrum disorders. BMC Med Genet 2009; 10: 7.
310. Gong X, Jia M, Ruan Y, Shuang M, Liu J, Wu S et al. Association between the FOXP2 gene and autistic disorder in Chinese population. Am J Med Genet B Neuropsychiatr Genet 2004; 127B(1): 113-116.
311. Goodlin-Jones BL, Tassone F, Gane LW, Hagerman RJ. Autistic spectrum disorder and the fragile X premutation. J Dev Behav Pediatr 2004; 25(6): 392-398.
312. Goodman AB. A family history study of schizophrenia spectrum disorders suggests new candidate genes in schizophrenia and autism. Psychiatr Q 1994; 65(4): 287-297.
313. Grady DL, Harxhi A, Smith M, Flodman P, Spence MA, Swanson JM et al. Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific. Am J Med Genet B Neuropsychiatr Genet 2005; 136B(1): 33-35.

314. Graf WD, Marin-Garcia J, Gao HG, Pizzo S, Naviaux RK, Markusic D et al. Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation. J Child Neurol 2000; 15(6): 357-361.

315. Greenberg DA, Hodge SE, Sowinski J, Nicoll D. Excess of twins among affected sibling pairs with autism: implications for the etiology of autism. Am J Hum Genet 2001; 69(5): 1062-1067.
316. Gregg JP, Lit L, Baron CA, Hertz-Picciotto I, Walker W, Davis RA et al. Gene expression changes in children with autism. Genomics 2008; 91(1): 22-29.
317. Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med 2009; 7: 62.
318. Grigorenko EL, Han SS, Yrigollen CM, Leng L, Mizue Y, Anderson GM et al. Macrophage migration inhibitory factor and autism spectrum disorders. Pediatrics 2008; 122(2): e438-445.
319. Grimbacher B, Dutra AS, Holland SM, Fischer RE, Pao M, Gallin JI et al. Analphoid marker chromosome in a patient with hyper-IgE syndrome, autism, and mild mental retardation. Genet Med 1999; 1(5): 213-218.
320. Guerini FR, Bolognesi E, Manca S, Sotgiu S, Zanzottera M, Agliardi C et al. Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders. Hum Immunol 2009; 70(3): 184-190.

321. Guerini FR, Manca S, Sotgiu S, Tremolada S, Zanzottera M, Agliardi C et al. A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder. Hum Immunol 2006; 67(1-2): 108-117.
322. Guhathakurta S, Ghosh S, Sinha S, Chatterjee A, Ahmed S, Chowdhury SR et al. Serotonin transporter promoter variants: Analysis in Indian autistic and control population. Brain Res 2006;


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