-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
DOI 10.1038/nrg2346, PII NRG2346
-
Abrahams, B.S., &, Geschwind, D.H., (2008). Advances in autism genetics: On the threshold of a new neurobiology. Nature Reviews. Genetics, 9, 341-355. (Pubitemid 351556064)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
77950899212
-
Connecting genes to brain in the autism spectrum disorders
-
Abrahams, B.S., &, Geschwind, D.H., (2010). Connecting genes to brain in the autism spectrum disorders. Archives of Neurology, 67, 395-399.
-
(2010)
Archives of Neurology
, vol.67
, pp. 395-399
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
3
-
-
0030879482
-
Imprinted expression of the murine angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
DOI 10.1038/ng0997-75
-
Albrecht, U., Sutcliffe, J.S., Cattanach, B.M., Beechey, C.V., Armstrong, D., Eichele, G., Beaudet, A.L., (1997). Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nature Genetics, 17, 75-78. (Pubitemid 27377535)
-
(1997)
Nature Genetics
, vol.17
, Issue.1
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
Beechey, C.V.4
Armstrong, D.5
Eichele, G.6
Beaudet, A.L.7
-
4
-
-
34447286464
-
Hyperresponsive sensory patterns in young children with autism, developmental delay, and typical development
-
Baranek, G.T., Boyd, B.A., Poe, M.D., David, F.J., &, Watson, L.R., (2007). Hyperresponsive sensory patterns in young children with autism, developmental delay, and typical development. American Journal of Mental Retardation, 112, 233-245.
-
(2007)
American Journal of Mental Retardation
, vol.112
, pp. 233-245
-
-
Baranek, G.T.1
Boyd, B.A.2
Poe, M.D.3
David, F.J.4
Watson, L.R.5
-
5
-
-
34447319904
-
Evaluation of autism traits in Angelman syndrome: A resource to unfold autism genes
-
DOI 10.1007/s10048-007-0086-0
-
Bonati, M.T., Russo, S., Finelli, P., Valsecchi, M.R., Cogliati, F., Cavalleri, F., et al., (2007). Evaluation of autism traits in Angelman syndrome: A resource to unfold autism genes. Neurogenetics, 8, 169-178. (Pubitemid 47051010)
-
(2007)
Neurogenetics
, vol.8
, Issue.3
, pp. 169-178
-
-
Bonati, M.T.1
Russo, S.2
Finelli, P.3
Valsecchi, M.R.4
Cogliati, F.5
Cavalleri, F.6
Roberts, W.7
Elia, M.8
Larizza, L.9
-
6
-
-
77951600825
-
Sensory features and repetitive behaviors in children with autism and developmental delays
-
Boyd, B.A., Baranek, G.T., Sideris, J., Poe, M.D., Watson, L.R., Patten, E., et al., (2010). Sensory features and repetitive behaviors in children with autism and developmental delays. Autism Research, 3, 78-87.
-
(2010)
Autism Research
, vol.3
, pp. 78-87
-
-
Boyd, B.A.1
Baranek, G.T.2
Sideris, J.3
Poe, M.D.4
Watson, L.R.5
Patten, E.6
-
7
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook, E.H., Jr., Lindgren, V., Leventhal, B.L., Courchesne, R., Lincoln, A., Shulman, C., et al., (1997). Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. American Journal of Human Genetics, 60, 928-934. (Pubitemid 27146502)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.4
, pp. 928-934
-
-
Cook Jr., E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
8
-
-
77953537460
-
Mechanism-based approaches to treating fragile X
-
Dolen, G., Carpenter, R.L., Ocain, T.D., &, Bear, M.F., (2010). Mechanism-based approaches to treating fragile X. Pharmacology and Therapeutics, 127, 78-93.
-
(2010)
Pharmacology and Therapeutics
, vol.127
, pp. 78-93
-
-
Dolen, G.1
Carpenter, R.L.2
Ocain, T.D.3
Bear, M.F.4
-
9
-
-
67349130116
-
Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioral disturbances
-
Doornbos, M., Sikkema-Raddatz, B., Ruijvenkamp, C.A., Dijkhuizen, T., Bijlsma, E.K., Gijsbers, A.C., et al., (2009). Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioral disturbances. European Journal of Medical Genetics, 52, 108-115.
-
(2009)
European Journal of Medical Genetics
, vol.52
, pp. 108-115
-
-
Doornbos, M.1
Sikkema-Raddatz, B.2
Ruijvenkamp, C.A.3
Dijkhuizen, T.4
Bijlsma, E.K.5
Gijsbers, A.C.6
-
10
-
-
50449083328
-
Behavior in Prader-Willi syndrome: Relationship to genetic subtypes and age
-
Dykens, E.M., &, Roof, E., (2008). Behavior in Prader-Willi syndrome: Relationship to genetic subtypes and age. Journal of Child Psychology and Psychiatry, 49, 1001-1008.
-
(2008)
Journal of Child Psychology and Psychiatry
, vol.49
, pp. 1001-1008
-
-
Dykens, E.M.1
Roof, E.2
-
11
-
-
77957374544
-
A neurodevelopmental survey of Angelman Syndrome with genotype-phenotype correlations
-
Gentile, J.K., Tan, W.H., Horowitz, L.T., Bacino, C.A., Skinner, S.A., Barbieri-Welge, R., â∥, Peters, S.U., (2010). A neurodevelopmental survey of Angelman Syndrome with genotype-phenotype correlations. Journal of Developmental and Behavioral Pediatrics, 31, 592-601.
-
(2010)
Journal of Developmental and Behavioral Pediatrics
, vol.31
, pp. 592-601
-
-
Gentile, J.K.1
Tan, W.H.2
Horowitz, L.T.3
Bacino, C.A.4
Skinner, S.A.5
Barbieri-Welge, R.6
Peters, S.U.7
-
12
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner, J.T., Wang, K., Cai, G., Korvatska, O., Kim, C.E., Wood, S., et al., (2009). Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature, 459, 569-573.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
-
13
-
-
44849109297
-
A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithms
-
Gotham, K., Risi, S., Dawson, G., Tager-Flusberg, H., Joseph, R., Carter, A., et al., (2008). A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithms. Journal of the American Academy of Child and Adolescent Psychiatry, 47, 642-651.
-
(2008)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.47
, pp. 642-651
-
-
Gotham, K.1
Risi, S.2
Dawson, G.3
Tager-Flusberg, H.4
Joseph, R.5
Carter, A.6
-
14
-
-
34147123692
-
The autism diagnostic observation schedule: Revised algorithms for improved diagnostic validity
-
DOI 10.1007/s10803-006-0280-1
-
Gotham, K., Risi, S., Pickles, A., &, Lord, C., (2007). The Autism Diagnostic Observation Schedule: Revised algorithms for improved diagnostic validity. Journal of Autism and Developmental Disorders, 37, 613-627. (Pubitemid 46571734)
-
(2007)
Journal of Autism and Developmental Disorders
, vol.37
, Issue.4
, pp. 613-627
-
-
Gotham, K.1
Risi, S.2
Pickles, A.3
Lord, C.4
-
15
-
-
77955701221
-
Autism spectrum disorders and epigenetics
-
Grafodatskaya, D., Chung, B., Szatmari, P., &, Weksberg, R., (2010). Autism spectrum disorders and epigenetics. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 794-809.
-
(2010)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.49
, pp. 794-809
-
-
Grafodatskaya, D.1
Chung, B.2
Szatmari, P.3
Weksberg, R.4
-
16
-
-
84855829012
-
-
Unpublished test, Children's Hospital, Boston
-
Hanson, E., Jackson, L., &, Hundley, R., (2007). The Behavior and Sensory Interests Questionnaire. Unpublished test, Children's Hospital, Boston.
-
(2007)
The Behavior and Sensory Interests Questionnaire
-
-
Hanson, E.1
Jackson, L.2
Hundley, R.3
-
17
-
-
77958487589
-
Cognitive and behavioral characterization of 16p11.2 deletion syndrome
-
Hanson, E., Nasir, R.H., Fong, A., Lian, A., Hundley, R., Shen, Y., et al., (2010). Cognitive and behavioral characterization of 16p11.2 deletion syndrome. Journal of Developmental and Behavioral Pediatrics, 31, 649-657.
-
(2010)
Journal of Developmental and Behavioral Pediatrics
, vol.31
, pp. 649-657
-
-
Hanson, E.1
Nasir, R.H.2
Fong, A.3
Lian, A.4
Hundley, R.5
Shen, Y.6
-
18
-
-
84894454320
-
A solution to limitations of cognitive testing in children with intellectual disabilities: The case of fragile X syndrome
-
Hessl, D., Nguyen, D.V., Green, C., Chavez, A., Tassone, F., Hagerman, R.J., et al., (2009). A solution to limitations of cognitive testing in children with intellectual disabilities: The case of fragile X syndrome. Journal of Neurodevelopmental Disorders, 1, 33-45.
-
(2009)
Journal of Neurodevelopmental Disorders
, vol.1
, pp. 33-45
-
-
Hessl, D.1
Nguyen, D.V.2
Green, C.3
Chavez, A.4
Tassone, F.5
Hagerman, R.J.6
-
19
-
-
77951206469
-
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
-
Hogart, A., Wu, D., LaSalle, J.M., &, Schanen, N.C., (2010). The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Diseases, 38, 181-191.
-
(2010)
Neurobiology of Diseases
, vol.38
, pp. 181-191
-
-
Hogart, A.1
Wu, D.2
Lasalle, J.M.3
Schanen, N.C.4
-
20
-
-
54949144402
-
The autistic neuron: Troubled translation?
-
Kelleher, R.J., III, &, Bear, M.F., (2008). The autistic neuron: Troubled translation? Cell, 135, 401-406.
-
(2008)
Cell
, vol.135
, pp. 401-406
-
-
Kelleher Iii, R.J.1
Bear, M.F.2
-
21
-
-
0031012849
-
UBE3A/E6-AP mutations cause Angelman syndrome
-
DOI 10.1038/ng0197-70
-
Kishino, T., Lalande, M., &, Wagstaff, J., (1997). UBE3A/E6-AP mutations cause Angelman syndrome. Nature Genetics, 15, 70-73. (Pubitemid 27014952)
-
(1997)
Nature Genetics
, vol.15
, Issue.1
, pp. 70-73
-
-
Kishino, T.1
Lalande, M.2
Wagstaff, J.3
-
22
-
-
64549117853
-
The autism spectrum: Definitions, assessment and diagnoses
-
Lord, C., &, Bishop, S.L., (2009). The autism spectrum: Definitions, assessment and diagnoses. British Journal of Hospital Medicine (London), 70, 132-135.
-
(2009)
British Journal of Hospital Medicine (London)
, vol.70
, pp. 132-135
-
-
Lord, C.1
Bishop, S.L.2
-
23
-
-
33644678754
-
Prader-Willi syndrome: Intellectual abilities and behavioural features by genetic subtype
-
DOI 10.1111/j.1469-7610.2005.01520.x
-
Milner, K.M., Craig, E.E., Thompson, R.J., Veltman, M.W., Thomas, N.S., Roberts, S., et al., (2005). Prader-Willi syndrome: Intellectual abilities and behavioral features by genetic subtype. Journal of Child Psychology and Psychiatry, 46, 1089-1096. (Pubitemid 44201556)
-
(2005)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.46
, Issue.10
, pp. 1089-1096
-
-
Milner, K.M.1
Craig, E.E.2
Thompson, R.J.3
Veltman, M.W.M.4
Simon Thomas, N.5
Roberts, S.6
Bellamy, M.7
Curran, S.R.8
Sporikou, C.M.J.9
Bolton, P.F.10
-
24
-
-
70350430194
-
Autism spectrum disorders in genetic syndromes: Implications for diagnosis, intervention and understanding the wider autism spectrum disorder population
-
Moss, J., &, Howlin, P., (2009). Autism spectrum disorders in genetic syndromes: Implications for diagnosis, intervention and understanding the wider autism spectrum disorder population. Journal of Intellectual Disability Research, 53, 852-873.
-
(2009)
Journal of Intellectual Disability Research
, vol.53
, pp. 852-873
-
-
Moss, J.1
Howlin, P.2
-
25
-
-
34547731978
-
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways
-
DOI 10.1093/hmg/ddm116
-
Nishimura, Y., Martin, C.L., Vazquez-Lopez, A., Spence, S.J., Alvarez-Retuerto, A.I., Sigman, M., et al., (2007). Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Human Molecular Genetics, 16, 1682-1698. (Pubitemid 47241828)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.14
, pp. 1682-1698
-
-
Nishimura, Y.1
Martin, C.L.2
Vazquez-Lopez, A.3
Spence, S.J.4
Alvarez-Retuerto, A.I.5
Sigman, M.6
Steindler, C.7
Pellegrini, S.8
Schanen, N.C.9
Warren, S.T.10
Geschwind, D.H.11
-
26
-
-
9444274771
-
Autism in Angelman syndrome: Implications for autism research
-
DOI 10.1111/j.1399-0004.2004.00362.x
-
Peters, S.U., Beaudet, A.L., Madduri, N., &, Bacino, C.A., (2004). Autism in Angelman syndrome: Implications for autism research. Clinical Genetics, 66, 530-536. (Pubitemid 39562016)
-
(2004)
Clinical Genetics
, vol.66
, Issue.6
, pp. 530-536
-
-
Peters, S.U.1
Beaudet, A.L.2
Madduri, N.3
Bacino, C.A.4
-
27
-
-
4444255037
-
Cognitive and adaptive behavior profiles of children with Angelman syndrome
-
DOI 10.1002/ajmg.a.30065
-
Peters, S.U., Goddard-Finegold, J., Beaudet, A.L., Madduri, N., Turcich, M., &, Bacino, C.A., (2004). Cognitive and adaptive behavior profiles of children with Angelman syndrome. American Journal of Medical Genetics. Part A, 128A, 110-113. (Pubitemid 39162929)
-
(2004)
American Journal of Medical Genetics
, vol.128 A
, Issue.2
, pp. 110-113
-
-
Peters, S.U.1
Goddard-Finegold, J.2
Beaudet, A.L.3
Madduri, N.4
Turcich, M.5
Bacino, C.A.6
-
28
-
-
79952587863
-
Alterations in white matter pathways in Angelman syndrome
-
Peters, S.U., Kaufmann, W.E., Bacino, C.A., Anderson, A.W., Adapa, P., Chu, Z., et al., (2011). Alterations in white matter pathways in Angelman syndrome. Developmental Medicine and Child Neurology, 53, 361-367.
-
(2011)
Developmental Medicine and Child Neurology
, vol.53
, pp. 361-367
-
-
Peters, S.U.1
Kaufmann, W.E.2
Bacino, C.A.3
Anderson, A.W.4
Adapa, P.5
Chu, Z.6
-
29
-
-
34548185218
-
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: Molecular characterization and genotype-phenotype correlations
-
DOI 10.1038/sj.ejhg.5201859, PII 5201859
-
Sahoo, T., Bacino, C.A., German, J.R., Shaw, C.A., Bird, L.M., Kimonis, V., et al., (2007). Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: Molecular characterization and genotype-phenotype correlations. European Journal of Human Genetics, 15, 943-949. (Pubitemid 47308470)
-
(2007)
European Journal of Human Genetics
, vol.15
, Issue.9
, pp. 943-949
-
-
Sahoo, T.1
Bacino, C.A.2
German, J.R.3
Shaw, C.A.4
Bird, L.M.5
Kimonis, V.6
Anselm, I.7
Waisbren, S.8
Beaudet, A.L.9
Peters, S.U.10
-
30
-
-
33745242295
-
Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: Genotype-phenotype correlations
-
DOI 10.1136/jmg.2005.036913
-
Sahoo, T., Peters, S.U., Madduri, N.S., Glaze, D.G., German, J.R., Bird, L.M., et al., (2006). Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: Genotype-phenotype correlations. Journal of Medical Genetics, 43, 512-516. (Pubitemid 43927326)
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.6
, pp. 512-516
-
-
Sahoo, T.1
Peters, S.U.2
Madduri, N.S.3
Glaze, D.G.4
German, J.R.5
Bird, L.M.6
Barbieri-Welge, R.7
Bichell, T.J.8
Beaudet, A.L.9
Bacino, C.A.10
-
31
-
-
78149301263
-
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
-
Scott-Van Zeeland, A.A., Abrahams, B.S., Alvarez-Retuerto, A.I., Sonnenblick, L.I., Rudie, J.D., Ghahremani, D., et al., (2010). Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Science Translational Medicine, 2, 56ra80.
-
(2010)
Science Translational Medicine
, vol.2
-
-
Scott-Van Zeeland, A.A.1
Abrahams, B.S.2
Alvarez-Retuerto, A.I.3
Sonnenblick, L.I.4
Rudie, J.D.5
Ghahremani, D.6
-
32
-
-
0028964542
-
Behavior problems in Angelman syndrome
-
Summers, J.A., Allison, D.B., Lynch, P.S., &, Sandler, L., (1995). Behavior problems in Angelman syndrome. Journal of Intellectual Disability Research, 39, 97-106.
-
(1995)
Journal of Intellectual Disability Research
, vol.39
, pp. 97-106
-
-
Summers, J.A.1
Allison, D.B.2
Lynch, P.S.3
Sandler, L.4
-
33
-
-
77953260190
-
Confirmed rare copy number variants implicate novel genes in schizophrenia
-
Tam, G.W., van de Lagemaat, L.N., Redon, R., Strathdee, K.E., Croning, M.D., Malloy, M.P., et al., (2010). Confirmed rare copy number variants implicate novel genes in schizophrenia. Biochemical Society Transactions, 38, 445-451.
-
(2010)
Biochemical Society Transactions
, vol.38
, pp. 445-451
-
-
Tam, G.W.1
Van De Lagemaat, L.N.2
Redon, R.3
Strathdee, K.E.4
Croning, M.D.5
Malloy, M.P.6
-
34
-
-
78650675939
-
Angelman syndrome: Mutations influence features in early childhood
-
Tan, W.H., Bacino, C.A., Skinner, S.A., Anselm, I., Barbieri-Welge, R., Bauer-Carlin, A., et al., (2011). Angelman syndrome: Mutations influence features in early childhood. American Journal of Medical Genetics. Part A, 155A, 81-90.
-
(2011)
American Journal of Medical Genetics. Part A
, vol.155 A
, pp. 81-90
-
-
Tan, W.H.1
Bacino, C.A.2
Skinner, S.A.3
Anselm, I.4
Barbieri-Welge, R.5
Bauer-Carlin, A.6
-
35
-
-
3042635551
-
Autism in Angelman syndrome: An exploration of comorbidity
-
DOI 10.1177/1362361304042720
-
Trillingsgaard, A., &, Ostergaard, J.R., (2004). Autism in Angelman syndrome: An exploration of comorbidity. Autism, 8, 163-174. (Pubitemid 38801761)
-
(2004)
Autism
, vol.8
, Issue.2
, pp. 163-174
-
-
Trillingsgaard, A.1
Ostergaard, J.R.2
-
36
-
-
77958192422
-
Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures
-
Utari, A., Chonchaiya, W., Rivera, S.M., Schneider, A., Hagerman, R.J., Faradz, S.M., et al., (2010). Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures. American Journal on Intellectual and Developmental Disabilities, 115, 433-443.
-
(2010)
American Journal on Intellectual and Developmental Disabilities
, vol.115
, pp. 433-443
-
-
Utari, A.1
Chonchaiya, W.2
Rivera, S.M.3
Schneider, A.4
Hagerman, R.J.5
Faradz, S.M.6
-
37
-
-
77952686118
-
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder
-
van der Zwaag, B., Staal, W.G., Hochstenbach, R., Poot, M., Spierenburg, H.A., de Jonge, M.V., et al., (2010). A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, 153B, 960-966.
-
(2010)
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
, vol.153 B
, pp. 960-966
-
-
Van Der Zwaag, B.1
Staal, W.G.2
Hochstenbach, R.3
Poot, M.4
Spierenburg, H.A.5
De Jonge, M.V.6
-
38
-
-
10044281472
-
Phenotypic variability in Angelman syndrome: Comparison among different deletion classes and between deletion and UPD subjects
-
DOI 10.1038/sj.ejhg.5201264
-
Varela, M.C., Kok, F., Otto, P.A., &, Koiffmann, C.P., (2004). Phenotypic variability in Angelman syndrome: Comparison among different deletion classes and between deletion and UPD subjects. European Journal of Human Genetics, 12, 987-992. (Pubitemid 39600125)
-
(2004)
European Journal of Human Genetics
, vol.12
, Issue.12
, pp. 987-992
-
-
Varela, M.C.1
Kok, F.2
Otto, P.A.3
Koiffmann, C.P.4
-
39
-
-
33845238728
-
Sensory processing patterns in persons with Angelman syndrome
-
Walz, N.C., &, Baranek, G.T., (2006). Sensory processing patterns in persons with Angelman syndrome. American Journal of Occupational Therapy, 60, 472-479. (Pubitemid 44859806)
-
(2006)
American Journal of Occupational Therapy
, vol.60
, Issue.4
, pp. 472-479
-
-
Walz, N.C.1
Baranek, G.T.2
-
41
-
-
33644865491
-
Angelman syndrome 2005: Updated consensus for diagnostic criteria
-
DOI 10.1002/ajmg.a.31074
-
Williams, C.A., Beaudet, A.L., Clayton-Smith, J., Knoll, J.H., Kyllerman, M., Laan, L.A., et al., (2006). Angelman syndrome 2005: Updated consensus for diagnostic criteria. American Journal of Medical Genetics. Part A, 140, 413-418. (Pubitemid 43376311)
-
(2006)
American Journal of Medical Genetics
, vol.140 A
, Issue.5
, pp. 413-418
-
-
Williams, C.A.1
Beaudet, A.L.2
Clayton-Smith, J.3
Knoll, J.H.4
Kyllerman, M.5
Laan, L.A.6
Magenis, R.E.7
Moncla, A.8
Schinzel, A.A.9
Summers, J.A.10
Wagstaff, J.11
-
42
-
-
67349178189
-
Ube3a is required for experience-dependent maturation of the neocortex
-
Yashiro, K., Riday, T.T., Condon, K.H., Roberts, A.C., Bernardo, D.R., Prakash, R., et al., (2009). Ube3a is required for experience-dependent maturation of the neocortex. Nature Neuroscience, 12 (6), 777-83.
-
(2009)
Nature Neuroscience
, vol.12
, Issue.6
, pp. 777-783
-
-
Yashiro, K.1
Riday, T.T.2
Condon, K.H.3
Roberts, A.C.4
Bernardo, D.R.5
Prakash, R.6
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