-
6
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
The Autism Genome Project Consortium
-
The Autism Genome Project Consortium, Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature Genetics 2007 39 3 319 328
-
(2007)
Nature Genetics
, vol.39
, Issue.3
, pp. 319-328
-
-
-
12
-
-
33751257500
-
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
-
Jacquemont M.-L., Sanlaville D., Redon R., Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders Journal of Medical Genetics 2006 43 11 843 849
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.11
, pp. 843-849
-
-
Jacquemont, M.-L.1
Sanlaville, D.2
Redon, R.3
-
14
-
-
0038238370
-
The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism
-
Castermans D., Wilquet V., Parthoens E., The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism Journal of Medical Genetics 2003 40 5 352 356
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.5
, pp. 352-356
-
-
Castermans, D.1
Wilquet, V.2
Parthoens, E.3
-
15
-
-
0036993811
-
Identification of novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins
-
Sultana R., Yu C.-E., Yu J., Identification of novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins Genomics 2002 80 2 129 134
-
(2002)
Genomics
, vol.80
, Issue.2
, pp. 129-134
-
-
Sultana, R.1
Yu, C.-E.2
Yu, J.3
-
16
-
-
0021932002
-
Chromosome abnormalities in infantile autism and other childhood psychoses: A population study of 66 cases
-
Gillberg C., Wahlström J., Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases Developmental Medicine and Child Neurology 1985 27 3 293 304
-
(1985)
Developmental Medicine and Child Neurology
, vol.27
, Issue.3
, pp. 293-304
-
-
Gillberg, C.1
Wahlström, J.2
-
17
-
-
3042542935
-
Chromosomal anomalies in individuals with autism: A strategy towards the identification of genes involved in autism
-
Castermans D., Wilquet V., Steyaert J., van de Ven W., Fryns J.-P., Devriendt K., Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism Autism 2004 8 2 141 161
-
(2004)
Autism
, vol.8
, Issue.2
, pp. 141-161
-
-
Castermans, D.1
Wilquet, V.2
Steyaert, J.3
Van De Ven, W.4
Fryns, J.-P.5
Devriendt, K.6
-
18
-
-
0031565936
-
Chromosome abnormalities in human beings
-
McFadden D. E., Friedman J. M., Chromosome abnormalities in human beings Mutation Research 1997 396 1-2 129 140
-
(1997)
Mutation Research
, vol.396
, Issue.1-2
, pp. 129-140
-
-
McFadden, D.E.1
Friedman, J.M.2
-
20
-
-
14044275302
-
FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour
-
Finelli P., Natacci F., Bonati M. T., FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour Journal of Medical Genetics 2004 41 7 e90
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.7
, pp. 90
-
-
Finelli, P.1
Natacci, F.2
Bonati, M.T.3
-
21
-
-
0037156292
-
Duplication of chromosome region (16) (p11.2→p12.1) in a mother and daughter with mild mental retardation
-
Engelen J. J. M., de Die-Smulders C. E. M., Dirckx R., Duplication of chromosome region (16) (p11.2→p12.1) in a mother and daughter with mild mental retardation American Journal of Medical Genetics 2002 109 2 149 153
-
(2002)
American Journal of Medical Genetics
, vol.109
, Issue.2
, pp. 149-153
-
-
Engelen, J.J.M.1
De Die-Smulders, C.E.M.2
Dirckx, R.3
-
22
-
-
0031057918
-
De novo trisomy 16p
-
Carrasco Juan J. L., Cigudosa J. C., Otero Gómez A., Acosta Almeida M. T., García Miranda J. L., De novo trisomy 16p American Journal of Medical Genetics 1997 68 2 219 221
-
(1997)
American Journal of Medical Genetics
, vol.68
, Issue.2
, pp. 219-221
-
-
Carrasco Juan, J.L.1
Cigudosa, J.C.2
Otero Gómez, A.3
Acosta Almeida, M.T.4
García Miranda, J.L.5
-
23
-
-
34548246019
-
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: Identification of genetic markers of autistic spectrum disorders
-
Vorsanova S. G., Yurov I. Yu., Demidova I. A., Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders Neuroscience and Behavioral Physiology 2007 37 6 553 558
-
(2007)
Neuroscience and Behavioral Physiology
, vol.37
, Issue.6
, pp. 553-558
-
-
Vorsanova, S.G.1
Yurov, I.Yu.2
Demidova, I.A.3
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