-
2
-
-
0029867499
-
Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1085-1088
-
-
-
18
-
-
0026849567
-
Positional cloning: Let's not call it reverse any more
-
(1992)
Nat Genet
, vol.1
, pp. 3-6
-
-
Collins, F.S.1
-
19
-
-
0002046974
-
Evidence that Tourette syndrome gene is at 18 22.1
-
Human Genetics: Proceedings of the 7th International Congress of Human Genetics Abstract Part II, Vogel F, Sperling K, eds. Berlin: Springer
-
(1986)
, pp. 620
-
-
Comings, D.E.1
Comings, B.G.2
Dietz, G.3
-
26
-
-
0023094073
-
Gene location in Tourette syndrome
-
(1987)
Lancet
, vol.14
, pp. 627
-
-
Donnai1
-
35
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.2
Pizzuti, A.3
-
37
-
-
0030730805
-
D4 dopamine-receptor (DRD4) alleles and novelty seeking in substance-dependent, personality-disorder, and control subjects
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1144-1152
-
-
Gelernter, J.1
Kranzler, H.2
Coccaro, E.3
Siever, L.4
New, A.5
Mulgrew, C.L.6
-
49
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
59
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
61
-
-
0032859009
-
Incremental progress in developmental psychopathology: Simply complex
-
(1999)
Am J Psychiatry
, vol.156
, pp. 1495-1498
-
-
Leckman, J.1
-
63
-
-
0032403843
-
Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method
-
(1998)
Biol Psychiatry
, vol.44
, pp. 1160-1165
-
-
Li, T.1
Vallada, H.P.2
Liu, X.3
-
65
-
-
0030068024
-
Molecular genetics of human blood pressure variation
-
(1996)
Science
, vol.272
, pp. 676-680
-
-
Lifton, R.P.1
-
69
-
-
0033569931
-
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families: The International Molecular Genetic Study of Autism Consortium
-
(1999)
Am J Med Genet
, vol.88
, pp. 492-496
-
-
Maestrini, E.1
Lai, C.2
Marlow, A.3
-
76
-
-
0032807087
-
Quantitative trait loci analysis for the differences in susceptibility to atherosclerosis and diabetes between inbred mouse strains C57BL/6J and C57BLKS/J
-
(1999)
J Lipid Res
, vol.40
, pp. 1328-1335
-
-
Mu, J.L.1
Naggert, J.K.2
Svenson, K.L.3
-
77
-
-
0027474137
-
Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: A review
-
(1993)
Am J Med Genet
, vol.46
, pp. 16-25
-
-
Nicholls, R.D.1
-
81
-
-
85031606605
-
-
Analysis of Human Genetic Linkage. Baltimore: Johns Hopkins University Press
-
(1991)
-
-
Ott, J.1
-
84
-
-
0004694846
-
-
Tourette's Syndrome: Tics, Obsessions, Compulsions, Leckman JF, Cohen DJ, eds. New York: Wiley
-
(1999)
, pp. 194-212
-
-
Pauls, D.L.1
Alsobrook, J.P.2
Gelernter, J.3
Leckman, J.F.4
-
85
-
-
0022515798
-
The inheritance of Gilles de la Tourette's syndrome and associated behaviors: Evidence for autosomal dominant transmission
-
(1986)
N Engl J Med
, vol.315
, pp. 993-997
-
-
Pauls, D.L.1
Leckman, J.F.2
-
87
-
-
0031409125
-
Molecular background of the Finnish disease heritage
-
(1997)
Ann Med
, vol.29
, pp. 553-556
-
-
Peltonen, L.1
-
88
-
-
0000877874
-
The detection of autosomal linkage data which consists of pairs of brothers and sisters of unspecified parentage
-
(1935)
Ann Eugen
, vol.6
, pp. 133-138
-
-
Penrose, L.S.1
-
91
-
-
0025019555
-
Linkage strategies for genetically complex traits, I: Multilocus models
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
92
-
-
0025008677
-
Linkage strategies for genetically complex traits, II: The power of affected relative pairs
-
(1990)
Am J Hum Genet
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
93
-
-
0025020461
-
Linkage strategies for genetically complex traits, III: The effect of marker polymorphism on analysis of affected relative pairs
-
(1990)
Am J Hum Genet
, vol.46
, pp. 242-253
-
-
Risch, N.1
-
96
-
-
0029001682
-
Extreme discordant sib pairs for mapping quantitative trait loci in humans
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
118
-
-
85031609703
-
Cloning of a candidate gene (ARG1) from the breakpoint of t(7;20) in an autistic twin pair
-
Abstracts of the Annual Meeting of the American Society for Human Genetics, program no. 230
-
(1999)
-
-
Sultana, R.1
Yu, J.2
Raskind, W.3
Disteche, C.4
-
120
-
-
0033365190
-
A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1428-1436
-
-
-
122
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
-
125
-
-
0032217057
-
Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: Heterogeneity owing to diagnostic subtype and severity
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1767-1776
-
-
Waldman, I.D.1
Rowe, D.C.2
Abramowitz, A.3
-
127
-
-
85031609995
-
Nongenetic factors associated with the expression of Tourette's syndrome
-
Proceedings of the 34th Annual Meeting of the American Academy of Child and Adolescent Psychiatry
-
(1987)
-
-
Walkup, J.T.1
Leckman, J.F.2
Price, R.A.3
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