Indexed keywords
AUTISM;
CELL HETEROGENEITY;
CHILDHOOD DISEASE;
CHROMOSOME DUPLICATION;
CHROMOSOME POLYMORPHISM;
GENETIC RISK;
GENETIC SUSCEPTIBILITY;
HERITABILITY;
HUMAN;
PRIORITY JOURNAL;
REVIEW;
RISK ASSESSMENT;
ARTICLE;
CHILD;
CHROMOSOME 15;
GENE DELETION;
GENE DUPLICATION;
GENETIC PREDISPOSITION;
GENETICS;
AUTISTIC DISORDER;
CHILD;
CHROMOSOMES, HUMAN, PAIR 15;
GENE DELETION;
GENE DUPLICATION;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
1
0035829969
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
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2
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Association between a GABRB3 polymorphism and autism
JD Buxbaum JM Silverman CJ Smith Association between a GABRB3 polymorphism and autism Mol Psychiatry 7 2002 311 316
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Mol Psychiatry , vol.7
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3
0033651946
Prader-Willi and Angelman syndromes: sister imprinted disorders
SB Cassidy E Dykens CA Williams Prader-Willi and Angelman syndromes: sister imprinted disorders Am J Med Genet 97 2000 136 146
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4
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Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
EH Cook Jr V Lindgren BL Leventhal Autism or atypical autism in maternally but not paternally derived proximal 15q duplication Am J Hum Genet 60 1997 928 934
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5
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Are jigsaw puzzle skills “spared” in persons with Prader-Willi syndrome?
EM Dykens Are jigsaw puzzle skills “spared” in persons with Prader-Willi syndrome? J Child Psychol Psychiatry 43 2002 343 352
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Genetics of autism: complex aetiology for a heterogeneous disorder
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7
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Mutation screening and transmission disequilibrium study of ATP10C in autism
SJ Kim LB Herzing J Veenstra-Vander Weele Mutation screening and transmission disequilibrium study of ATP10C in autism Am J Med Genet 114 2002 137 143
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Am J Med Genet , vol.114
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Herzing, LB2
Veenstra-Vander Weele, J3
8
0035417396
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
EL Nurmi Y Bradford Y Chen Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families Genomics 77 2001 105 113
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Genomics , vol.77
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Nurmi, EL1
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9
0027792161
Clinical and molecular analysis of five inv dup(15) patients
WP Robinson F Binkert R Gine Clinical and molecular analysis of five inv dup(15) patients Eur J Hum Genet 1993 1 1993 37 50
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Eur J Hum Genet 1993 , vol.1
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Robinson, WP1
Binkert, F2
Gine, R3
10
18344374001
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
Y Shao KL Raiford CM Wolpert Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder Am J Hum Genet 70 2002 1058 1061
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Am J Hum Genet , vol.70
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Raiford, KL2
Wolpert, CM3
11
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Candidate-gene approaches for studying complex genetic traits: practical considerations
HK Tabor N Risch RM Myers Candidate-gene approaches for studying complex genetic traits: practical considerations Nat Rev Genet 3 2002 1 7
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Nat Rev Genet , vol.3
, pp. 1-7
Tabor, HK1
Risch, N2
Myers, RM3
