Publications by authors named "Lyndsey Connell"

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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters.
Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, Joanna McParland, Michael G Pike

Am J Med Genet A· November 2011

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Duplication of the EFNB1 gene in familial hypertelorism: imbalance in ephrin-B1 expression and abnormal phenotypes in humans and mice.
Christian Babbs, Helen S Stewart, Louise J Williams, Lyndsey Connell, Anne Goriely

Hum Mutat· August 2011

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Two generations of identical twins with ELN deletion.
Jasper Katumba-Lunyenya, Lyndsey Connell, Talal Farha, Rosemary Radley-Smith, Satish Adwani

BMJ Case Rep· July 2011

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Diagnosis of Pallister-Killian syndrome by array comparative genome hybridization from a spleen sample.
Victoria Harrison, Rosy Williams, Lyndsey Connell, Usha Kini

Clin Dysmorphol· January 2011

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