-
1
-
-
77956671613
-
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: Genotype-phenotype correlation
-
Abu-Amero, K.K., Hellani, A.M., Salih, M.A., Seidahmed, M.Z., Elmalik, T.S., Zidan, G., &, Bosley, T.M., (2010). A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: Genotype-phenotype correlation. BMC Medical Genetics, 11, 135.
-
(2010)
BMC Medical Genetics
, vol.11
, pp. 135
-
-
Abu-Amero, K.K.1
Hellani, A.M.2
Salih, M.A.3
Seidahmed, M.Z.4
Elmalik, T.S.5
Zidan, G.6
Bosley, T.M.7
-
2
-
-
33745818375
-
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The special needs and autism project (SNAP)
-
Baird, G., Simonoff, E., Pickles, A., Chandler, S., Loucas, T., Meldrum, D., &, Charman, T., (2006). Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The special needs and autism project (SNAP). Lancet, 368, 210-215.
-
(2006)
Lancet
, vol.368
, pp. 210-215
-
-
Baird, G.1
Simonoff, E.2
Pickles, A.3
Chandler, S.4
Loucas, T.5
Meldrum, D.6
Charman, T.7
-
3
-
-
34547923133
-
The behavioural phenotype of Cornelia de Lange syndrome: A study of 56 individuals
-
Basile, E., Villa, L., Selicorni, A., &, Molteni, M., (2007). The behavioural phenotype of Cornelia de Lange syndrome: A study of 56 individuals. Journal of Intellectual Disability Research, 51, 671-681.
-
(2007)
Journal of Intellectual Disability Research
, vol.51
, pp. 671-681
-
-
Basile, E.1
Villa, L.2
Selicorni, A.3
Molteni, M.4
-
4
-
-
0017144546
-
Epidemiology of cornelia de lange syndrome
-
Beck, B., (1976). Epidemiology of cornelia de lange syndrome. Acta Paediatrics Scandanavia, 65, 631-638.
-
(1976)
Acta Paediatrics Scandanavia
, vol.65
, pp. 631-638
-
-
Beck, B.1
-
5
-
-
0021948046
-
Mortality, pathological findings and causes of death in the de lange syndrome
-
Beck, B., &, Fenger, K., (1985). Mortality, pathological findings and causes of death in the de lange syndrome. Acta Paediatrics Scandanavia, 74, 765-769.
-
(1985)
Acta Paediatrics Scandanavia
, vol.74
, pp. 765-769
-
-
Beck, B.1
Fenger, K.2
-
6
-
-
0032835107
-
Behavioral phenotype of Cornelia de Lange syndrome
-
Berney, T.P., Ireland, M., &, Burn, J., (1999). Behavioral phenotype of Cornelia de Lange syndrome. Archives of Diseases in Childhood, 81, 333-336.
-
(1999)
Archives of Diseases in Childhood
, vol.81
, pp. 333-336
-
-
Berney, T.P.1
Ireland, M.2
Burn, J.3
-
7
-
-
33745909174
-
Genotype-phenotype correlations of 39 patients with Cornelia de Lange syndrome: The Dutch experience
-
Bhuiyan, Z.A., Klein, M., Hammond, P., van Haeringen, A., Mannens, M.A.M., Van Berckelaer-Onnes, I., &, Hennekam, R.C.M., (2006). Genotype-phenotype correlations of 39 patients with Cornelia de Lange syndrome: The Dutch experience. Journal of Medical Genetics, 46, 568-575.
-
(2006)
Journal of Medical Genetics
, vol.46
, pp. 568-575
-
-
Bhuiyan, Z.A.1
Klein, M.2
Hammond, P.3
Van Haeringen, A.4
Mannens, M.A.M.5
Van Berckelaer-Onnes, I.6
Hennekam, R.C.M.7
-
8
-
-
0013358720
-
Repetitive behaviors and social-communicative impairments in autism: Implications for developmental theory and diagnosis
-
J.A. Burack, T. Charman, N. Yirmiya, & P.R. Zelazo (Eds.),. New Jersey: Lawrence Erlbaum Associates
-
Charman, T., &, Swettenham, J., (2001). Repetitive behaviors and social-communicative impairments in autism: Implications for developmental theory and diagnosis. In, J.A. Burack, T. Charman, N. Yirmiya, &, P.R. Zelazo, (Eds.), The Development of Autism: Perspectives from Theory and Research (pp. 325-345). New Jersey: Lawrence Erlbaum Associates.
-
(2001)
The Development of Autism: Perspectives from Theory and Research
, pp. 325-345
-
-
Charman, T.1
Swettenham, J.2
-
9
-
-
18144424836
-
Outcome at 7 years of children diagnosed with autism at age 2: Predictive validity of assessments conducted at 2 and 3 years of age and pattern of symptom change over time
-
Charman, T., Taylor, E., Drew, A., Cockerill, H., Brown, J., &, Baird, G., (2005). Outcome at 7 years of children diagnosed with autism at age 2: Predictive validity of assessments conducted at 2 and 3 years of age and pattern of symptom change over time. Journal of Child Psychology and Psychiatry, 46, 500-513.
-
(2005)
Journal of Child Psychology and Psychiatry
, vol.46
, pp. 500-513
-
-
Charman, T.1
Taylor, E.2
Drew, A.3
Cockerill, H.4
Brown, J.5
Baird, G.6
-
10
-
-
70349592376
-
Low mood and social anxiety in Cornelia de Lange syndrome
-
Collis, L., Oliver, C., &, Moss, J., (2006). Low mood and social anxiety in Cornelia de Lange syndrome. Journal of Intellectual Disability Research, 50, 791-800.
-
(2006)
Journal of Intellectual Disability Research
, vol.50
, pp. 791-800
-
-
Collis, L.1
Oliver, C.2
Moss, J.3
-
11
-
-
33847308551
-
Fragile X syndrome and autism: Common developmental pathways?
-
Cornish, K., Turk, J., &, Levitas, A., (2007). Fragile X syndrome and autism: Common developmental pathways? Current Peadistric Reviews, 3, 61-68.
-
(2007)
Current Peadistric Reviews
, vol.3
, pp. 61-68
-
-
Cornish, K.1
Turk, J.2
Levitas, A.3
-
12
-
-
33847196427
-
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation
-
Deardorff, M.A., Kaur, M., Yaeger, D., Rampuria, A., Korolev, S., Pie, J., ⋯, Krantz, I.D, (2007). Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation. American Journal of Human Genetics, 80, 485-494.
-
(2007)
American Journal of Human Genetics
, vol.80
, pp. 485-494
-
-
Deardorff, M.A.1
Kaur, M.2
Yaeger, D.3
Rampuria, A.4
Korolev, S.5
Pie, J.6
Krantz, I.D.7
-
13
-
-
0003700595
-
-
(2nd edn). Windsor: NFER-Nelson
-
Dunn, L.M., Dunn, L.M., Whetton, C., &, Burley, J., (1997). The British Picture Vocabulary Scale (2nd edn). Windsor: NFER-Nelson.
-
(1997)
The British Picture Vocabulary Scale
-
-
Dunn, L.M.1
Dunn, L.M.2
Whetton, C.3
Burley, J.4
-
15
-
-
84863816193
-
Autism, intellectual disability and molecular-genetic aspects associated with subtelomeric rearrangements
-
Fisch, G., Grossfeld, P.D., Youngblom, J., Simensen, R., &, Battaglia, A., (2010). Autism, intellectual disability and molecular-genetic aspects associated with subtelomeric rearrangements. Journal of Intellectual Disability Research, 54, 886.
-
(2010)
Journal of Intellectual Disability Research
, vol.54
, pp. 886
-
-
Fisch, G.1
Grossfeld, P.D.2
Youngblom, J.3
Simensen, R.4
Battaglia, A.5
-
16
-
-
0032804766
-
The epidemiology of autism: A review
-
Fombonne, E., (1999). The epidemiology of autism: A review. Psychological Medicine, 29, 769-786.
-
(1999)
Psychological Medicine
, vol.29
, pp. 769-786
-
-
Fombonne, E.1
-
18
-
-
4544253309
-
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations
-
Gillis, L.A., McCallum, J., Kaur, M., DeScipio, C., Yaeger, D., Mariani, A., ⋯, Krantz, I.D., (2004). NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations. American Journal of Human Genetics, 75, 610-623.
-
(2004)
American Journal of Human Genetics
, vol.75
, pp. 610-623
-
-
Gillis, L.A.1
McCallum, J.2
Kaur, M.3
Descipio, C.4
Yaeger, D.5
Mariani, A.6
Krantz, I.D.7
-
19
-
-
0027429313
-
Survey of speech and language skills with prognostic indicators in 116 patients with Cornelia de Lange syndrome
-
Goodban, M.T., (1993). Survey of speech and language skills with prognostic indicators in 116 patients with Cornelia de Lange syndrome. American Journal of Medical Genetics, 47, 1059-1063.
-
(1993)
American Journal of Medical Genetics
, vol.47
, pp. 1059-1063
-
-
Goodban, M.T.1
-
20
-
-
33748960624
-
Social escape behaviours in individuals with fragile X syndrome
-
Hall, S., deBernardis, M., &, Reiss, A., (2006). Social escape behaviours in individuals with fragile X syndrome. Journal of Autism and Developmental Disorders, 36, 935-947.
-
(2006)
Journal of Autism and Developmental Disorders
, vol.36
, pp. 935-947
-
-
Hall, S.1
Debernardis, M.2
Reiss, A.3
-
21
-
-
77956176282
-
Autism in fragile X syndrome: A category mistake?
-
Hall, S., Lightbody, A.A., Hirt, M., Rezvani, A., &, Reiss, A.L., (2010). Autism in fragile X syndrome: A category mistake? Journal of the American Academy of Child and Adolescent Psychiatry, 54, 921-933.
-
(2010)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.54
, pp. 921-933
-
-
Hall, S.1
Lightbody, A.A.2
Hirt, M.3
Rezvani, A.4
Reiss, A.L.5
-
22
-
-
56549107680
-
The 'fractionable autism triad': A review of evidence from behavioural, genetic, cognitive and neural research
-
Happé, F., &, Ronald, A., (2008). The 'fractionable autism triad': A review of evidence from behavioural, genetic, cognitive and neural research. Neuropsychological Review, 18, 287-304.
-
(2008)
Neuropsychological Review
, vol.18
, pp. 287-304
-
-
Happé, F.1
Ronald, A.2
-
23
-
-
33749032127
-
Time to give up on a single explanation for autism
-
Happé, F., Ronald, A., &, Plomin, R., (2006). Time to give up on a single explanation for autism. Nature Neuroscience, 9, 1218-1220.
-
(2006)
Nature Neuroscience
, vol.9
, pp. 1218-1220
-
-
Happé, F.1
Ronald, A.2
Plomin, R.3
-
24
-
-
3042549224
-
Using the Social Communication Questionnaire to identify 'autistic spectrum' disorders associated with other genetic conditions: Findings from a study of individuals with Cohen syndrome
-
Howlin, P., &, Karpf, J., (2004). Using the Social Communication Questionnaire to identify 'autistic spectrum' disorders associated with other genetic conditions: findings from a study of individuals with Cohen syndrome. Autism, 8, 175-182.
-
(2004)
Autism
, vol.8
, pp. 175-182
-
-
Howlin, P.1
Karpf, J.2
-
25
-
-
0027429307
-
De Lange syndrome: A clinical review of 310 individuals
-
Jackson, L., Kline, A.D., Barr, M., &, Koch, S., (1993). de Lange syndrome: A clinical review of 310 individuals. American Journal of Medical Genetics, 47, 940-946.
-
(1993)
American Journal of Medical Genetics
, vol.47
, pp. 940-946
-
-
Jackson, L.1
Kline, A.D.2
Barr, M.3
Koch, S.4
-
26
-
-
2642542322
-
Cornelia de lange syndrome is caused by mutations in NIBPL, the human homolog of Drosophila melanogaster Nipped-B
-
Krantz, I.D., McCallum, J., DeScipio, C., Kaur, M., Gillis, L.A., Yaeger, D., ⋯, Jackson, L.G., (2004). Cornelia de lange syndrome is caused by mutations in NIBPL, the human homolog of Drosophila melanogaster Nipped-B. Nature Genetics, 6, 631-635.
-
(2004)
Nature Genetics
, vol.6
, pp. 631-635
-
-
Krantz, I.D.1
McCallum, J.2
Descipio, C.3
Kaur, M.4
Gillis, L.A.5
Yaeger, D.6
Jackson, L.G.7
-
27
-
-
1842855895
-
Autism and intellectual disability: A study of prevalence on a sample of the Italian population
-
La Malfa, G., Lassi, S., Bertelli, M., Salvini, R., &, Placidi, G.F., (2004). Autism and intellectual disability: a study of prevalence on a sample of the Italian population. Journal of Intellectual Disability Research, 48, 262-267.
-
(2004)
Journal of Intellectual Disability Research
, vol.48
, pp. 262-267
-
-
La Malfa, G.1
Lassi, S.2
Bertelli, M.3
Salvini, R.4
Placidi, G.F.5
-
28
-
-
84863851976
-
Behavioral assessment of social anxiety in females with turner of fragile X syndrome
-
Lesniak-Karpiak, K., Mazzocco, M.M.M., &, Ross, J.L., (2003). Behavioral assessment of social anxiety in females with turner of fragile X syndrome. Journal of Autism and Developmental Disorders, 36, 935-947.
-
(2003)
Journal of Autism and Developmental Disorders
, vol.36
, pp. 935-947
-
-
Lesniak-Karpiak, K.1
Mazzocco, M.M.M.2
Ross, J.L.3
-
29
-
-
0003428096
-
-
Los Angeles: Western Psychological Services
-
Lord, C., Rutter, M., DiLavore, P.C., &, Risi, S., (2000). The Autism Diagnostic Observation Schedule (ADOS). Los Angeles: Western Psychological Services.
-
(2000)
The Autism Diagnostic Observation Schedule (ADOS)
-
-
Lord, C.1
Rutter, M.2
Dilavore, P.C.3
Risi, S.4
-
30
-
-
34547749941
-
A two-year prospective follow-up study of community-based early intensive behavioural intervention and specialist nursery provision for children with autism spectrum disorders
-
Magiati, I., Charman, T., &, Howlin, P., (2007). A two-year prospective follow-up study of community-based early intensive behavioural intervention and specialist nursery provision for children with autism spectrum disorders. Journal of Child Psychology and Psychiatry, 48, 803-812.
-
(2007)
Journal of Child Psychology and Psychiatry
, vol.48
, pp. 803-812
-
-
Magiati, I.1
Charman, T.2
Howlin, P.3
-
31
-
-
79952448509
-
Patterns of change in children with autism spectrum disorders who received community based comprehensive interventions in their pre-school years: A seven year follow up study
-
Magiati, I., Moss, J., Charman, T., &, Howlin, P., (2011). Patterns of change in children with autism spectrum disorders who received community based comprehensive interventions in their pre-school years: A seven year follow up study. Research in Autism Spectrum Disorders, 5, 1016-1027.
-
(2011)
Research in Autism Spectrum Disorders
, vol.5
, pp. 1016-1027
-
-
Magiati, I.1
Moss, J.2
Charman, T.3
Howlin, P.4
-
32
-
-
48149089002
-
Research review: What is the association between the social-communication element of autism and repetitive interests, behaviours and activities?
-
Mandy, W.P.L., &, Skuse, D.H., (2008). Research review: What is the association between the social-communication element of autism and repetitive interests, behaviours and activities? Journal of Child Psychology and Psychiatry, 49, 795-808.
-
(2008)
Journal of Child Psychology and Psychiatry
, vol.49
, pp. 795-808
-
-
Mandy, W.P.L.1
Skuse, D.H.2
-
33
-
-
20944451704
-
Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome
-
Miyake, N., Visser, R., Kinoshita, A., Yoshiura, K.I., Niikawa, N., Kondoh, T., ⋯, Kurosawa, K., (2005). Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome. American Journal of Medical Genetics, 135, 103-105.
-
(2005)
American Journal of Medical Genetics
, vol.135
, pp. 103-105
-
-
Miyake, N.1
Visser, R.2
Kinoshita, A.3
Yoshiura, K.I.4
Niikawa, N.5
Kondoh, T.6
Kurosawa, K.7
-
34
-
-
84863851727
-
Delineating the profile of autism spectrum disorder in Cornelia de Lange syndrome
-
Moss, J., Hall, S., Collis, L., Arron, K., Burbidge, C., Richards, C., &, Oliver, C., (2010). Delineating the profile of autism spectrum disorder in Cornelia de Lange syndrome. Journal of Intellectual Disability Research, 54, 888.
-
(2010)
Journal of Intellectual Disability Research
, vol.54
, pp. 888
-
-
Moss, J.1
Hall, S.2
Collis, L.3
Arron, K.4
Burbidge, C.5
Richards, C.6
Oliver, C.7
-
35
-
-
70350430194
-
Invited annotation: Autism spectrum disorders in genetic syndromes: Implications for diagnosis, intervention and understanding the wider ASD population
-
Moss, J., &, Howlin, P., (2009). Invited annotation: Autism spectrum disorders in genetic syndromes: Implications for diagnosis, intervention and understanding the wider ASD population. Journal of Intellectual Disability Research, 53, 852-872.
-
(2009)
Journal of Intellectual Disability Research
, vol.53
, pp. 852-872
-
-
Moss, J.1
Howlin, P.2
-
36
-
-
84863824293
-
The assessment and presentation of autism spectrum disorder and associated characteristics in individuals with severe intellectual disability and genetic syndromes
-
J. Burack, R. Hodapp, G. Iarocci, & E. Zigler, (Ed.) New York: Oxford University Press
-
Moss, J., Howlin, P., &, Oliver, C., (2011). The assessment and presentation of autism spectrum disorder and associated characteristics in individuals with severe intellectual disability and genetic syndromes. In, J. Burack, R. Hodapp, G. Iarocci, &, E. Zigler, (Ed.), The Oxford Handbook of Intellectual Disability and Development (pp. 275-299). New York: Oxford University Press.
-
(2011)
The Oxford Handbook of Intellectual Disability and Development
, pp. 275-299
-
-
Moss, J.1
Howlin, P.2
Oliver, C.3
-
37
-
-
49949152363
-
Stability of the autism diagnostic interview- revised from pre-school to elementary school in children with autism spectrum disorders
-
Moss, J., Magiati, I., Charman, T., &, Howlin, P., (2008a). Stability of the autism diagnostic interview- revised from pre-school to elementary school in children with autism spectrum disorders. Journal of Autism and Developmental Disorders, 38, 1081-1091.
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, pp. 1081-1091
-
-
Moss, J.1
Magiati, I.2
Charman, T.3
Howlin, P.4
-
38
-
-
48749120257
-
Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes
-
Moss, J., Oliver, C., Wilkie, L., Berg, K., Kaur, G., &, Cornish, K., (2008b). Prevalence of autism spectrum phenomenology in Cornelia de Lange and Cri du Chat syndromes. American Journal of Mental Retardation, 113, 278-291.
-
(2008)
American Journal of Mental Retardation
, vol.113
, pp. 278-291
-
-
Moss, J.1
Oliver, C.2
Wilkie, L.3
Berg, K.4
Kaur, G.5
Cornish, K.6
-
39
-
-
0037227002
-
Towards a behavioral phenotype for Rett syndrome
-
Mount, R.H., Hastings, R.P., Reilly, S., Cass, H., &, Charman, T., (2003). Towards a behavioral phenotype for Rett syndrome. American Journal on Mental Retardation, 1, 1-12.
-
(2003)
American Journal on Mental Retardation
, vol.1
, pp. 1-12
-
-
Mount, R.H.1
Hastings, R.P.2
Reilly, S.3
Cass, H.4
Charman, T.5
-
40
-
-
33646379870
-
X-linked cornelia de lange syndrome owing to SMC1L1 mutations
-
Musio, A., Selicorni, A., Focarelli, M.L., Gervasini, C., Milani, D., Russo, S., ⋯, Larizza, L., (2006). X-linked cornelia de lange syndrome owing to SMC1L1 mutations. Nature Genetics, 38, 528-530.
-
(2006)
Nature Genetics
, vol.38
, pp. 528-530
-
-
Musio, A.1
Selicorni, A.2
Focarelli, M.L.3
Gervasini, C.4
Milani, D.5
Russo, S.6
Larizza, L.7
-
42
-
-
57449106631
-
The behavioral phenotype of Cornelia de Lange syndrome: Case control study
-
Oliver, C., Arron, K., Sloneem, J., &, Hall, S., (2008). The behavioral phenotype of Cornelia de Lange syndrome: Case control study. British Journal of Psychiatry, 193, 466-470.
-
(2008)
British Journal of Psychiatry
, vol.193
, pp. 466-470
-
-
Oliver, C.1
Arron, K.2
Sloneem, J.3
Hall, S.4
-
43
-
-
79961170673
-
Delineation of behavioral phenotypes in genetic syndromes. Comparison of autism spectrum disorder, affect and hyperactivity
-
Oliver, C., Berg, K., Moss, J., Arron K., & Burbidge, C., (2011). Delineation of behavioral phenotypes in genetic syndromes. Comparison of autism spectrum disorder, affect and hyperactivity. Journal of Autism and Developmental Disorders, 41, 1019-1032.
-
(2011)
Journal of Autism and Developmental Disorders
, vol.41
, pp. 1019-1032
-
-
Oliver, C.1
Berg, K.2
Moss, J.3
Arron, K.4
Burbidge, C.5
-
44
-
-
33746314832
-
Searching for ways out of the autism maze: Genetic, epigenetic and environmental clues
-
Persico, A.M., &, Bourgeron, T., (2006). Searching for ways out of the autism maze: Genetic, epigenetic and environmental clues. Trends in Neuroscience, 29, 349-358.
-
(2006)
Trends in Neuroscience
, vol.29
, pp. 349-358
-
-
Persico, A.M.1
Bourgeron, T.2
-
45
-
-
77957895378
-
Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
-
Quintero-Rivera, F., Sharifi-Hannauer, P., &, Martinez-Agosto, J.A., (2010). Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review. American Journal of Medical Genetics Part A, 152a, 2459-2467.
-
(2010)
American Journal of Medical Genetics Part A
, vol.152 A
, pp. 2459-2467
-
-
Quintero-Rivera, F.1
Sharifi-Hannauer, P.2
Martinez-Agosto, J.A.3
-
46
-
-
70349598257
-
Social anxiety in Cornelia de Lange syndrome
-
Richards, C., Moss, J., O'Farrell, L., Kaur, G., &, Oliver, C., (2009). Social anxiety in Cornelia de Lange syndrome. Journal of Autism and Developmental Disorders, 39, 1155-1162.
-
(2009)
Journal of Autism and Developmental Disorders
, vol.39
, pp. 1155-1162
-
-
Richards, C.1
Moss, J.2
O'Farrell, L.3
Kaur, G.4
Oliver, C.5
-
47
-
-
33748417617
-
Combining information from multiple sources in the diagnosis of autism spectrum disorders
-
Risi, S., Lord, C., Gotham, K., Corsello, C., Chrysler, C., Szatmari, P., Cook, E., Leventhal, B., &, Pickles, A., (2006). Combining information from multiple sources in the diagnosis of autism spectrum disorders. American Academy of Child and Adolescent Psychiatry, 45, 1094-1103.
-
(2006)
American Academy of Child and Adolescent Psychiatry
, vol.45
, pp. 1094-1103
-
-
Risi, S.1
Lord, C.2
Gotham, K.3
Corsello, C.4
Chrysler, C.5
Szatmari, P.6
Cook, E.7
Leventhal, B.8
Pickles, A.9
-
48
-
-
34748907163
-
Social approach and autistic behavior in children with fragile X syndrome
-
Roberts, J.E., Weisenfeld, L.A.H., Hatton, D.D., Health, M., &, Kaufmann, W.E., (2007). Social approach and autistic behavior in children with fragile X syndrome. Journal of Autism and Developmental Disorders, 37, 1748-1760.
-
(2007)
Journal of Autism and Developmental Disorders
, vol.37
, pp. 1748-1760
-
-
Roberts, J.E.1
Weisenfeld, L.A.H.2
Hatton, D.D.3
Health, M.4
Kaufmann, W.E.5
-
49
-
-
0842297288
-
-
Los Angeles: Western Psychological Services
-
Rutter, M., Bailey, A., Lord, C., &, Berument, S.K., (2003). The Social Communication Questionnaire. Los Angeles: Western Psychological Services.
-
(2003)
The Social Communication Questionnaire
-
-
Rutter, M.1
Bailey, A.2
Lord, C.3
Berument, S.K.4
-
50
-
-
34447628063
-
Rethinking the nature of genetic vulnerability to autistic spectrum disorders
-
Skuse, D.H., (2007). Rethinking the nature of genetic vulnerability to autistic spectrum disorders. Trends in Genetics, 23, 387-395.
-
(2007)
Trends in Genetics
, vol.23
, pp. 387-395
-
-
Skuse, D.H.1
-
51
-
-
0003895711
-
-
Circle Pines, MN: American Guidance Service (AGS)
-
Sparrow, S.S., Balla, D., &, Cicchetti, D.V., (1984). Vineland Adaptive Behavior Scales. Circle Pines, MN: American Guidance Service (AGS).
-
(1984)
Vineland Adaptive Behavior Scales
-
-
Sparrow, S.S.1
Balla, D.2
Cicchetti, D.V.3
-
52
-
-
2642565901
-
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
-
Tonkin, E.T., Wang, T., Lisgo, S., Bamshad, M.J., &, Strachan, T., (2004). NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nature Genetics, 6, 636-641.
-
(2004)
Nature Genetics
, vol.6
, pp. 636-641
-
-
Tonkin, E.T.1
Wang, T.2
Lisgo, S.3
Bamshad, M.J.4
Strachan, T.5
-
53
-
-
3042635551
-
Autism in Angelman syndrome: An exploration of comorbidity
-
Trillingsgaard, A., &, Ostergaard, J.R., (2004). Autism in Angelman syndrome: An exploration of comorbidity. Autism: International Journal of Research and Practice, 8, 163-174.
-
(2004)
Autism: International Journal of Research and Practice
, vol.8
, pp. 163-174
-
-
Trillingsgaard, A.1
Ostergaard, J.R.2
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