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A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. Fisher SE, et al. Among authors: marlow aj. Am J Hum Genet. 2002 May;70(5):1183-96. doi: 10.1086/340112. Epub 2002 Mar 28. Am J Hum Genet. 2002. PMID: 11923911 Free PMC article.
A genomewide linkage screen for relative hand skill in sibling pairs.
Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP. Francks C, et al. Among authors: marlow aj. Am J Hum Genet. 2002 Mar;70(3):800-5. doi: 10.1086/339249. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774074 Free PMC article.
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. Francks C, et al. Among authors: marlow aj. Am J Hum Genet. 2004 Dec;75(6):1046-58. doi: 10.1086/426404. Epub 2004 Oct 22. Am J Hum Genet. 2004. PMID: 15514892 Free PMC article.
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.
Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP. Maestrini E, et al. Am J Med Genet. 1999 Oct 15;88(5):492-6. doi: 10.1002/(sici)1096-8628(19991015)88:5<492::aid-ajmg11>3.0.co;2-x. Am J Med Genet. 1999. PMID: 10490705
Molecular genetic investigations of autism.
Maestrini E, Marlow AJ, Weeks DE, Monaco AP. Maestrini E, et al. Among authors: marlow aj. J Autism Dev Disord. 1998 Oct;28(5):427-37. doi: 10.1023/a:1026056522602. J Autism Dev Disord. 1998. PMID: 9813778 Review.
21 results