Paterson AD - Search Results

1

A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.

Zaidi SH, Peltekova V, Meyer S, Lindinger A, Paterson AD, Tsui LC, Faiyaz-Ul-Haque M, Teebi AS. Zaidi SH, et al. Among authors: paterson ad. Clin Genet. 2005 Feb;67(2):183-8. doi: 10.1111/j.1399-0004.2004.00391.x. Clin Genet. 2005. PMID: 15679832

2

The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23.

Lo B, Faiyaz-Ul-Haque M, Banwell B, Blaser S, Paterson AD, Tsui LC, Teebi AS. Lo B, et al. Among authors: paterson ad. Clin Genet. 2004 Feb;65(2):137-42. doi: 10.1111/j.0009-9163.2004.00201.x. Clin Genet. 2004. PMID: 14984473

3

Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22.

Chan EM, Bulman DE, Paterson AD, Turnbull J, Andermann E, Andermann F, Rouleau GA, Delgado-Escueta AV, Scherer SW, Minassian BA. Chan EM, et al. Among authors: paterson ad. J Med Genet. 2003 Sep;40(9):671-5. doi: 10.1136/jmg.40.9.671. J Med Genet. 2003. PMID: 12960212 Free PMC article.

4

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.

Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL. Vincent JB, et al. Among authors: paterson ad. Am J Hum Genet. 2000 Mar;66(3):819-29. doi: 10.1086/302803. Am J Hum Genet. 2000. PMID: 10712198 Free PMC article.

5

A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.

Héon E, Paterson AD, Fraser M, Billingsley G, Priston M, Balmer A, Schorderet DF, Verner A, Hudson TJ, Munier FL. Héon E, et al. Among authors: paterson ad. Am J Hum Genet. 2001 Mar;68(3):772-7. doi: 10.1086/318798. Epub 2001 Feb 5. Am J Hum Genet. 2001. PMID: 11179024 Free PMC article.

6

Age of diagnosis-based linkage analysis in type 1 diabetes.

Paterson AD, Petronis A. Paterson AD, et al. Eur J Hum Genet. 2000 Feb;8(2):145-8. doi: 10.1038/sj.ejhg.5200420. Eur J Hum Genet. 2000. PMID: 10757648

7

Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.

Loo JC, Paterson AD, Hao A, Shennan M, Peretz H, Sidi Y, Hogg D, Yakobson E. Loo JC, et al. Among authors: paterson ad. J Med Genet. 2005 May;42(5):e30. doi: 10.1136/jmg.2004.027300. J Med Genet. 2005. PMID: 15863662 Free PMC article. No abstract available.

8

Age and sex based genetic locus heterogeneity in type 1 diabetes.

Paterson AD, Petronis A. Paterson AD, et al. J Med Genet. 2000 Mar;37(3):186-91. doi: 10.1136/jmg.37.3.186. J Med Genet. 2000. PMID: 10699054 Free PMC article.

9

An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.

Vincent JB, Horike SI, Choufani S, Paterson AD, Roberts W, Szatmari P, Weksberg R, Fernandez B, Scherer SW. Vincent JB, et al. Among authors: paterson ad. J Med Genet. 2006 May;43(5):429-34. doi: 10.1136/jmg.2005.039693. Epub 2006 Mar 23. J Med Genet. 2006. PMID: 16556609 Free PMC article.

10

X-chromosome workshop.

Paterson AD. Paterson AD. Psychiatr Genet. 1998 Summer;8(2):121-6. doi: 10.1097/00041444-199800820-00017. Psychiatr Genet. 1998. PMID: 9686435

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