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Общее количество найденных документов : 36
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 1-20    21-36 
1.
Willcutt Erik G. Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder // Amer. J. Med. Genet., 2000. Vol. 96, N 3.-С.293-301

2.
No association of the DRD2 polymorphism and attention deficit hyperactivity disorder in the Irish population // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.488

3.
A family based candidate gene association study of attention deficit hyperactivity disorder // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.489

4.
A study of ADHD in a genetic isolate // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.487-488

5.
Naqvi Cole-Hughes macrocephaly syndrome and associated autistic manifestations // Amer. J. Med. Genet., 2000. Vol. 94, N 2.-С.149-152

6.
Naqvi Cole-Hughes macrocephaly syndrome and associated autistic manifestations // Amer. J. Med. Genet., 2000. Vol. 94, N 2.-С.149-152

7.
Family-based candidate gene association studies in ADHD // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.470-471

8.
Thapar A. Examining the genetic basis of ADHD related behaviours and conduct problems // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.470

9.
ADHD symptoms in children with autistic disorder (AD) // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.475

10.
A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorders // Amer. J. Med. Genet., 1998. Vol. 81, N 6.-С.458

11.
Hay D.A. Comordibidity as a means of identifying genetic heterogeneity in ADHD // Amer. J. Med. Genet., 2000. Vol. 96, N 4.-С.470

12.
Bower B. Gene may alter Ritalin's effects in ADHD // Sci. News, 1999. Vol. 156, N 23.-С.359

13.
Cognitive and behavioral profile of fragile X boys: Correlations to molecular data // Amer. J. Med. Genet., 2000. Vol. 95, N 2.-С.150-156

14.
Behavioral phenotype in childhood type of dystrophia myotonica // Amer. J. Med. Genet., 2000. Vol. 96, N 6.-С.888-889

15.
Bower B. Gene may alter Ritalin's effects in ADHD // Sci. News, 1999. Vol. 156, N 23.-С.359

16.
Smalley Susan L. Refining the ADHD phenotype using affected sibling pair families // Amer. J. Med. Genet., 2001. Vol. 105, N 1.-С.31-33

17.
Genetic and environmental causes of covariation in interview assessments of disruptive behavior in child and adolescent twins // Behav. Genet., 2000. Vol. 30, N 4.-С.321-334

18.
Genetic and environmental causes of covariation in interview assessments of disruptive behavior in child and adolescent twins // Behav. Genet., 2000. Vol. 30, N 4.-С.321-334

19.
Coolidge Frederick L. Heritability and the comorbidity of attention deficit hyperactivity disorder with behavioral disorders and executive function deficits: A preliminary investigation // Dev. Neuropsychol., 2000. Vol. 17, N 3.-С.273-287

20.
Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder // Amer. J. Med. Genet., 2001. Vol. 105, N 1.-С.91-95

 1-20    21-36 
 




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