-
2
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med, 1995, 25:63-77.
-
(1995)
Psychol Med
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
-
4
-
-
0029926866
-
A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males
-
Haddad LA, Mingroni-Netto RC, Vianna-Morgante AM, et al. A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males. Hum Genet, 1996, 97:808-812.
-
(1996)
Hum Genet
, vol.97
, pp. 808-812
-
-
Haddad, L.A.1
Mingroni-Netto, R.C.2
Vianna-Morgante, A.M.3
-
5
-
-
0011819393
-
High-resolution chromosomal localization of human genes for amylase, proopiomelenocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization
-
Zabel BU, Naylor SL, Sakaguchi AY, et al. High-resolution chromosomal localization of human genes for amylase, proopiomelenocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization. Proc Natl Acad Sci U S A, 1983, 80:6932-6936.
-
(1983)
Proc Natl Acad Sci U S A
, vol.80
, pp. 6932-6936
-
-
Zabel, B.U.1
Naylor, S.L.2
Sakaguchi, A.Y.3
-
6
-
-
0032694507
-
Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine
-
Korenberg JR, Chen XN, Sun Z, et al. Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. Genome Res, 1999, 9:994-1001.
-
(1999)
Genome Res
, vol.9
, pp. 994-1001
-
-
Korenberg, J.R.1
Chen, X.N.2
Sun, Z.3
-
7
-
-
0028986730
-
Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization
-
Korenberg JR, Chen XN. Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization. Cytogenet Cell Genet, 1995, 69:196-200.
-
(1995)
Cytogenet Cell Genet
, vol.69
, pp. 196-200
-
-
Korenberg, J.R.1
Chen, X.N.2
-
8
-
-
0035653670
-
Genetics of autism: Complex aetiology for a heterogeneous disorder
-
Folstein SE, Rosen-Sheidley B. Genetics of autism: complex aetiology for a heterogeneous disorder. Nat Review Genet, 2001, 2:943-955.
-
(2001)
Nat Review Genet
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
9
-
-
0034045595
-
Association of a balanced chromosomal translocation (4;12) (q21.3;q15), affective disorder and autism
-
Nasr A, Roy M. Association of a balanced chromosomal translocation (4;12) (q21.3;q15), affective disorder and autism. J Intellect Disabil Res, 2000, 44(Pt 2):170-174.
-
(2000)
J Intellect Disabil Res
, vol.44
, Issue.PART 2
, pp. 170-174
-
-
Nasr, A.1
Roy, M.2
-
10
-
-
2542435173
-
A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-unit (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R
-
Ramanathan S, Woodroffe A, Flodman PL, 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-unit (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R. BMC Med Genet, 2004, 5:10.
-
(2004)
BMC Med Genet
, vol.5
, pp. 10
-
-
Ramanathan, S.1
Woodroffe, A.2
Flodman, P.L.3
-
11
-
-
0023906140
-
Partial 6p trisomy associated with infantile autism
-
Burd L, Martsolf JT, Kerbeshian J, et al. Partial 6p trisomy associated with infantile autism. Clin Genet, 1988, 33:356-359.
-
(1988)
Clin Genet
, vol.33
, pp. 356-359
-
-
Burd, L.1
Martsolf, J.T.2
Kerbeshian, J.3
-
12
-
-
2642549948
-
DNA sequence and analysis of human chromosome 9
-
Humphrey SJ, Oliver K, Hunt AR, et al. DNA sequence and analysis of human chromosome 9. Nature, 2004, 429:369-374.
-
(2004)
Nature
, vol.429
, pp. 369-374
-
-
Humphrey, S.J.1
Oliver, K.2
Hunt, A.R.3
-
13
-
-
0034606205
-
Analysis of a 1-megebase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
-
Smith M, Filipek PA, Wu C, et al. Analysis of a 1-megebase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13. Am J Med Genet, 2000, 96:765-770.
-
(2000)
Am J Med Genet
, vol.96
, pp. 765-770
-
-
Smith, M.1
Filipek, P.A.2
Wu, C.3
-
14
-
-
0034599736
-
Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31
-
Warburton P, Baird G, Chen W, et al. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. Am J Med Genet, 2000, 96:228-234.
-
(2000)
Am J Med Genet
, vol.96
, pp. 228-234
-
-
Warburton, P.1
Baird, G.2
Chen, W.3
-
15
-
-
10744231297
-
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features
-
Pescucci C, Meloni I, Bruttini M, et al. Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features. Clin Genet, 2003, 64:497-501.
-
(2003)
Clin Genet
, vol.64
, pp. 497-501
-
-
Pescucci, C.1
Meloni, I.2
Bruttini, M.3
|