Publications by authors named "Annette Cockwell"

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Investigation of the origins of human autosomal inversions.
N Simon Thomas, Victoria Bryant, Vivienne Maloney, Annette E Cockwell, Patricia A Jacobs

Hum Genet· July 2008

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In memoriam: Dr Marina Seabright.
John Barber, Annette Cockwell, Tony Herbert, Nick Dennis, John Harvey

Eur J Hum Genet· November 2007

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The origin of trisomy 13.
Heather E Hall, E Ricky Chan, Andrew Collins, LuAnn Judis, Sofia Shirley, Annette E Cockwell

Am J Med Genet A· October 2007

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Distribution of the D15Z1 copy number polymorphism.
Annette E Cockwell, Patricia A Jacobs, John A Crolla

Eur J Hum Genet· April 2007

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Mosaic trisomy 6 and maternal uniparental disomy 6 in a 23-week gestation fetus with atrioventricular septal defect.
Annette E Cockwell, Samantha J Baker, Margaret Connarty, Isabella E Moore, John A Crolla

Am J Med Genet A· March 2006

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Pallister-Killian syndrome: an unusual cause of epileptic spasms.
Rocio Sánchez-Carpintero, Ailsa McLellan, Lucio Parmeggiani, Annette E Cockwell, Richard J Ellis

Dev Med Child Neurol· November 2005

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A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.
Annette E Cockwell, Patricia A Jacobs, Sarah J Beal, John A Crolla

Hum Genet· March 2003

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Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.
Andrew M Fisher, N Simon Thomas, Annette Cockwell, Olga Stecko, Bronwyn Kerr

Hum Genet· September 2002

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