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Gregory J Fitzgibbon
Gregory J Fitzgibbon
St Mary's Hospital
Genetics
Chromosome
Medicine
Haploinsufficiency
Gene duplication
3
Papers
19
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A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion.
2011
American Journal of Medical Genetics Part A
Siddharth Banka
Gregory J Fitzgibbon
Lorraine Gaunt
Wendy J. Rankin
Jill Clayton-Smith
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Citations (3)
Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain
2009
Developmental Medicine & Child Neurology
Gregory J Fitzgibbon
Helen Kingston
Margaret Needham
Lorraine Gaunt
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Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report
2008
Journal of Medical Case Reports
Gregory J Fitzgibbon
Jill Clayton-Smith
Siddharth Banka
Susan J. Hamilton
Margaret Needham
Jonathan Dore
Jake T Miller
Gareth D Pawson
Lorraine Gaunt
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Citations (9)
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