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
: 611-615.

643. Pancrudo J, Shanske S, Coku J, Lu J, Mardach R, Akman O et al. Mitochondrial myopathy associated with a novel mutation in mtDNA. Neuromuscul Disord 2007; 17(8): 651-654.
644. Papanikolaou K, Paliokosta E, Gyftodimou J, Kolaitis G, Vgenopoulou S, Sarri C et al. A case of partial trisomy of chromosome 8p associated with autism. J Autism Dev Disord 2006; 36(5): 705-709.
645. Pasca SP, Dronca E, Kaucsar T, Craciun EC, Endreffy E, Ferencz BK et al. One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders. J Cell Mol Med 2009; 13(10): 4229-4238.
646. Pasca SP, Dronca E, Nemes B, Kaucsar T, Endreffy E, Iftene F et al. Paraoxonase 1 activities and polymorphisms in autism spectrum disorders. J Cell Mol Med 2010; 14(3): 600-607.
647. Payton JB, Steele MW, Wenger SL, Minshew NJ. The fragile X marker and autism in perspective. J Am Acad Child Adolesc Psychiatry 1989; 28(3): 417-421.

648. Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R, Bravaccio C et al. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. Mol Psychiatry 2001; 6(2): 150-159.

649. Persico AM, D'Agruma L, Zelante L, Militerni R, Bravaccio C, Schneider C et al. Enhanced APOE2 transmission rates in families with autistic probands. Psychiatr Genet 2004; 14(2): 73-82.
650. Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M et al. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Am J Med Genet 2000; 96(1): 123-127.
651. Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S et al. No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder. Psychiatr Genet 2001; 11(2): 99-103.
652. Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S et al. Adenosine deaminase alleles and autistic disorder: case-control and family-based association studies. Am J Med Genet 2000; 96(6): 784-790.
653. Persico AM, Pascucci T, Puglisi-Allegra S, Militerni R, Bravaccio C, Schneider C et al. Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. Mol Psychiatry 2002; 7(7): 795-800.

654. Persson C, Niklasson L, Oskarsdottir S, Johansson S, Jonsson R, Soderpalm E. Language skills in 5-8-year-old children with 22q11 deletion syndrome. Int J Lang Commun Disord 2006; 41(3): 313-333.

655. Pescucci C, Meloni I, Bruttini M, Ariani F, Longo I, Mari F et al. Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features. Clin Genet 2003; 64(6): 497-501.
656. Petek E, Schwarzbraun T, Noor A, Patel M, Nakabayashi K, Choufani S et al. Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. Mol Genet Genomics 2007; 277(1): 71-81.
657. Peters SU, Beaudet AL, Madduri N, Bacino CA. Autism in Angelman syndrome: implications for autism research. Clin Genet 2004; 66(6): 530-536.
658. Petersen MB, Vejerslev LO, Beck B. Trisomy 14 mosaicism in a 2 year old girl. J Med Genet 1986; 23(1): 86-88.
659. Peterson E, Schmidt GL, Tregellas JR, Winterrowd E, Kopelioff L, Hepburn S et al. A voxel-based morphometry study of gray matter in parents of children with autism. Neuroreport 2006; 17(12): 1289-1292.

660. Petit E, Herault J, Martineau J, Perrot A, Barthelemy C, Hameury L et al. Association study with two markers of a human homeogene in infantile autism. J Med Genet 1995; 32(4): 269-274.

661. Petit E, Herault J, Raynaud M, Cherpi C, Perrot A, Barthelemy C et al. X chromosome and infantile autism. Biol Psychiatry 1996; 40(6): 457-464.
662. Philippe A, Guilloud-Bataille M, Martinez M, Gillberg C, Rastam M, Sponheim E et al. Analysis of ten candidate genes in autism by association and linkage. Am J Med Genet 2002; 114(2): 125-128.
663. Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Rastam M, Sponheim E et al. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet 1999; 8(5): 805-812.
664. Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L et al. Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Mol Psychiatry 2005; 10(10): 950-960.
665. Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E et al. Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Med Genet 2007; 8: 74.

666. Piccione M, Antona V, Antona R, Gambino G, Pierluigi M, Malacarne M et al. Array-CGH defined chromosome 1p duplication in a patient with autism spectrum disorder, mild mental deficiency, and minor dysmorphic features. Am J Med Genet A 2010; 152A(2): 486-489.

667. Pickler L, Elias E. Genetic evaluation of the child with an autism spectrum disorder. Pediatr Ann 2009; 38(1): 26-29.
668. Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH et al. 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(3): 717-726.
669. Pilowsky T, Yirmiya N, Doppelt O, Gross-Tsur V, Shalev RS. Social and emotional adjustment of siblings of children with autism. J Child Psychol Psychiatry 2004; 45(4): 855-865.
670. Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466(7304): 368-372.
671. Piton A, Michaud JL, Peng H, Aradhya S, Gauthier J, Mottron L et al. Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Hum Mol Genet 2008; 17(24): 3965-3974.
672. Piven J, Palmer P. Cognitive deficits in parents from multiple-incidence autism families. J Child Psychol Psychiatry 1997; 38(8): 1011-1021.

673. Plank SM, Copeland-Yates SA, Sossey-Alaoui K, Bell JM, Schroer RJ, Skinner C et al. Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism. Am J Med Genet 2001; 105(5): 404-405.

674. Pons R, Andreu AL, Checcarelli N, Vila MR, Engelstad K, Sue CM et al. Mitochondrial DNA abnormalities and autistic spectrum disorders. J Pediatr 2004; 144(1): 81-85.
675. Poo-Arguelles P, Arias A, Vilaseca MA, Ribes A, Artuch R, Sans-Fito A et al. X-Linked creatine transporter deficiency in two patients with severe mental retardation and autism. J Inherit Metab Dis 2006; 29(1): 220-223.
676. Poon PM, Chen QL, Lai KY, Wong CK, Pang CP. CGG repeat interruptions in the FMR1 gene in patients with infantile autism. Clin Chem Lab Med 1998; 36(8): 649-653.
677. Poot M, Beyer V, Schwaab I, Damatova N, Van't Slot R, Prothero J et al. Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics 2010; 11(1): 81-89.
678. Prasad HC, Steiner JA, Sutcliffe JS, Blakely RD. Enhanced activity of human serotonin transporter variants associated with autism. Philos Trans R Soc Lond B Biol Sci 2009; 364(1514): 163-173.

679. Pueschel SM, Herman R, Groden G. Brief report: screening children with autism for fragile-X syndrome and phenylketonuria. J Autism Dev Disord 1985; 15(3): 335-338.

680. Qiao Y, Harvard C, Riendeau N, Fawcett C, Liu X, Holden JJ et al. Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability. Cytogenet Genome Res 2008; 123(1-4): 79-87.
681. Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ et al. Autism-associated familial microdeletion of Xp11.22. Clin Genet 2008; 74(2): 134-144.
682. Qiao Y, Riendeau N, Koochek M, Liu X, Harvard C, Hildebrand MJ et al. Phenomic determinants of genomic variation in autism spectrum disorders. J Med Genet 2009; 46(10): 680-688.
683. Qin J, Jia M, Wang L, Lu T, Ruan Y, Liu J et al. Association study of SHANK3 gene polymorphisms with autism in Chinese Han population. BMC Med Genet 2009; 10: 61.
684. Quintero-Rivera F, Sharifi-Hannauer P, Martinez-Agosto JA. Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review. Am J Med Genet A 2010; 152A(10): 2459-2467.

685. Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL et al. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Neurosci Lett 2004; 372(3): 209-214.

686. Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS et al. Lack of association between autism and SLC25A12. Am J Psychiatry 2006; 163(5): 929-931.
687. Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH et al. No association between the APOE gene and autism. Am J Med Genet B Neuropsychiatr Genet 2004; 125B(1): 57-60.
688. Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB et al. A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R. BMC Med Genet 2004; 5: 10.
689. Ramelli GP, Silacci C, Ferrarini A, Cattaneo C, Visconti P, Pescia G. Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study. Dev Med Child Neurol 2008; 50(12): 953-955.
690. Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP et al. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Ann Neurol 2009; 66(6): 771-782.

691. Ramoz N, Cai G, Reichert JG, Corwin TE, Kryzak LA, Smith CJ et al. Family-based association study of TPH1 and TPH2 polymorphisms in autism. Am J Med Genet B Neuropsychiatr Genet 2006; 141B(8): 861-867.

692. Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD. An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(7): 1152-1158.
693. Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E et al. Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism. Biol Psychiatry 2006; 60(2): 186-191.
694. Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL et al. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. Am J Psychiatry 2004; 161(4): 662-669.
695. Rasmussen K, Nielsen J, Sillesen I, Brask BH, Saldana-Garcia P. A bisatellited marker chromosome in a mentally retarded girl with infantile autism. Hereditas 1976; 82(1): 37-42.
696. Raznahan A, Pugliese L, Barker GJ, Daly E, Powell J, Bolton PF et al. Serotonin transporter genotype and neuroanatomy in autism spectrum disorders. Psychiatr Genet 2009; 19(3): 147-150.

697. Raznahan A, Toro R, Proitsi P, Powell J, Paus T, P FB et al. A functional polymorphism of the brain derived neurotrophic factor gene and cortical anatomy in autism spectrum disorder. J Neurodev Disord 2009; 1(3): 215-223.

698. Reddy KS. Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder. BMC Med Genet 2005; 6: 3.
699. Redfern RE, Daou MC, Li L, Munson M, Gericke A, Ross AH. A mutant form of PTEN linked to autism. Protein Sci 2010; 19(10): 1948-1956.
700. Rehnstrom K, Ylisaukko-oja T, Nieminen-von Wendt T, Sarenius S, Kallman T, Kempas E et al. Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome. J Med Genet 2006; 43(2): e6.
701. Rehnstrom K, Ylisaukko-oja T, Nummela I, Ellonen P, Kempas E, Vanhala R et al. Allelic variants in HTR3C show association with autism. Am J Med Genet B Neuropsychiatr Genet 2009; 150B(5): 741-746.
702. Rehnstrom K, Ylisaukko-Oja T, Vanhala R, von Wendt L, Peltonen L, Hovatta I. No association between common variants in glyoxalase 1 and autism spectrum disorders. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(1): 124-127.
703. Reiersen AM, Constantino JN, Grimmer M, Martin NG, Todd RD. Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Res Hum Genet 2008; 11(6): 579-585.

704. Richler E, Reichert JG, Buxbaum JD, McInnes LA. Autism and ultraconserved non-coding sequence on chromosome 7q. Psychiatr Genet 2006; 16(1): 19-23.

705. Rineer S, Finucane B, Simon EW. Autistic symptoms among children and young adults with isodicentric chromosome 15. Am J Med Genet 1998; 81(5): 428-433.
706. Rippon G, Brock J, Brown C, Boucher J. Disordered connectivity in the autistic brain: challenges for the "new psychophysiology". Int J Psychophysiol 2007; 63(2): 164-172.
707. Ritvo ER, Freeman BJ, Mason-Brothers A, Mo A, Ritvo AM. Concordance for the syndrome of autism in 40 pairs of afflicted twins. Am J Psychiatry 1985; 142(1): 74-77.
708. Ritvo ER, Spence MA, Freeman BJ, Mason-Brothers A, Mo A, Marazita ML. Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism. Am J Psychiatry 1985; 142(2): 187-192.
709. Robinson PD, Schutz CK, Macciardi F, White BN, Holden JJ. Genetically determined low maternal serum dopamine beta-hydroxylase levels and the etiology of autism spectrum disorders. Am J Med Genet 2001; 100(1): 30-36.

710. Rogers SJ, Wehner DE, Hagerman R. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr 2001; 22(6): 409-417.

711. Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C et al. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. J Autism Dev Disord 1999; 29(3): 195-201.
712. Romano V, Cali F, Mirisola M, Gambino G, R DA, Di Rosa P et al. Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients. Mol Psychiatry 2003; 8(8): 716-717.
713. Romano V, Cali F, Seidita G, Mirisola M, D'Anna RP, Gambino G et al. Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families. Psychiatr Genet 2005; 15(2): 149-150.
714. Ronald A, Butcher LM, Docherty S, Davis OS, Schalkwyk LC, Craig IW et al. A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples. Behav Genet 2010; 40(1): 31-45.
715. Ronald A, Happe F, Bolton P, Butcher LM, Price TS, Wheelwright S et al. Genetic heterogeneity between the three components of the autism spectrum: a twin study. J Am Acad Child Adolesc Psychiatry 2006; 45(6): 691-699.

716. Ronald A, Happe F, Plomin R. The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism. Dev Sci 2005; 8(5): 444-458.

717. Ronald A, Happe F, Plomin R. A twin study investigating the genetic and environmental aetiologies of parent, teacher and child ratings of autistic-like traits and their overlap. Eur Child Adolesc Psychiatry 2008; 17(8): 473-483.
718. Ronald A, Happe F, Price TS, Baron-Cohen S, Plomin R. Phenotypic and genetic overlap between autistic traits at the extremes of the general population. J Am Acad Child Adolesc Psychiatry 2006; 45(10): 1206-1214.
719. Ronald A, Larsson H, Anckarsater H, Lichtenstein P. A twin study of autism symptoms in Sweden. Mol Psychiatry 2010.
720. Ronald A, Simonoff E, Kuntsi J, Asherson P, Plomin R. Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample. J Child Psychol Psychiatry 2008; 49(5): 535-542.
721. Roohi J, DeVincent CJ, Hatchwell E, Gadow KD. Association of a monoamine oxidase-a gene promoter polymorphism with ADHD and anxiety in boys with autism spectrum disorder. J Autism Dev Disord 2009; 39(1): 67-74.

722. Roohi J, Montagna C, Tegay DH, Palmer LE, DeVincent C, Pomeroy JC et al. Disruption of contactin 4 in three subjects with autism spectrum disorder. J Med Genet 2009; 46(3): 176-182.

723. Roohi J, Tegay DH, Pomeroy JC, Burkett S, Stone G, Stanyon R et al. A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet 2008; 147B(4): 411-417.
724. Rosenfeld JA, Ballif BC, Torchia BS, Sahoo T, Ravnan JB, Schultz R et al. Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders. Genet Med 2010; 12(11): 694-702.
725. Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A et al. A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea. Eur J Med Genet 2008; 51(6): 631-638.
726. Russell G, Steer C, Golding J. Social and demographic factors that influence the diagnosis of autistic spectrum disorders. Soc Psychiatry Psychiatr Epidemiol 2010.
727. Russo AJ, Neville L, Wroge C. Low Serum Alpha-1 Antitrypsin (AAT) in Family Members of Individuals with Autism Correlates with PiMZ Genotype. Biomark Insights 2009; 4: 45-56.

728. Russo S, Marchi M, Cogliati F, Bonati MT, Pintaudi M, Veneselli E et al. Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes. Neurogenetics 2009; 10(3): 241-250.

729. Rutter M, Kreppner J, Croft C, Murin M, Colvert E, Beckett C et al. Early adolescent outcomes of institutionally deprived and non-deprived adoptees. III. Quasi-autism. J Child Psychol Psychiatry 2007; 48(12): 1200-1207.
730. Sabaratnam M, Murthy NV, Wijeratne A, Buckingham A, Payne S. Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome: a prospective ten-year follow-up study. Eur Child Adolesc Psychiatry 2003; 12(4): 172-177.
731. Sabaratnam M, Turk J, Vroegop P. Case report: autistic disorder and chromosomal abnormality 46, XX duplication (4) p12-p13. Eur Child Adolesc Psychiatry 2000; 9(4): 307-311.
732. Sabry MA, Farag TI. Chromosome 15q11-13 region and the autistic disorder. J Intellect Disabil Res 1998; 42 ( Pt 3): 259.
733. Sacco R, Papaleo V, Hager J, Rousseau F, Moessner R, Militerni R et al. Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1. BMC Med Genet 2007; 8: 11.

734. Sakurai T, Ramoz N, Reichert JG, Corwin TE, Kryzak L, Smith CJ et al. Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors. Psychiatr Genet 2006; 16(6): 251-257.

735. Sakurai T, Reichert J, Hoffman EJ, Cai G, Jones HB, Faham M et al. A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders. Autism Res 2008; 1(4): 251-257.
736. Saliba JR, Griffiths M. Brief report: autism of the Asperger type associated with an autosomal fragile site. J Autism Dev Disord 1990; 20(4): 569-575.
737. Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P et al. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. Am J Med Genet 1999; 88(5): 551-556.
738. Salyakina D, Ma DQ, Jaworski JM, Konidari I, Whitehead PL, Henson R et al. Variants in several genomic regions associated with asperger disorder. Autism Res 2010; 3(6): 303-310.
739. Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet 2005; 14(4): 483-492.
740. Sankar DV. Chromosome breakage in infantile autism. Dev Med Child Neurol 1970; 12(5): 572-575.

741. Sauter S, von Beust G, Burfeind P, Weise A, Starke H, Liehr T et al. Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]. Am J Med Genet A 2003; 120A(4): 533-536.

742. Sbacchi S, Acquadro F, Calo I, Cali F, Romano V. Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding. Curr Genomics 2010; 11(2): 136-145.
743. Schaefer GB, Lutz RE. Diagnostic yield in the clinical genetic evaluation of autism spectrum disorders. Genet Med 2006; 8(9): 549-556.
744. Schaefer GB, Starr L, Pickering D, Skar G, Dehaai K, Sanger WG. Array comparative genomic hybridization findings in a cohort referred for an autism evaluation. J Child Neurol 2010; 25(12): 1498-1503.
745. Schaevitz LR, Moriuchi JM, Nag N, Mellot TJ, Berger-Sweeney J. Cognitive and social functions and growth factors in a mouse model of Rett syndrome. Physiol Behav 2010; 100(3): 255-263.
746. Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E et al. Evidence for multiple loci from a genome scan of autism kindreds. Mol Psychiatry 2006; 11(11): 1049-1060, 1979.
747. Schinzel A. Autistic disorder and additional inv dup(15)(pter----q13) chromosome. Am J Med Genet 1990; 35(3): 447-448.

748. Schnetz-Boutaud NC, Anderson BM, Brown KD, Wright HH, Abramson RK, Cuccaro ML et al. Examination of tetrahydrobiopterin pathway genes in autism. Genes Brain Behav 2009; 8(8): 753-757.
749. Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M et al. Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet 1998;

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

The database is protected by copyright © 2017
send message

    Main page