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Margaret Barrow

Leicester Royal Infirmary

13

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Ophthalmological Aspects of Pierson Syndrome

2011 American Journal of Ophthalmology
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Ophthalmological Aspects of Pierson Syndrome

2008 American Journal of Ophthalmology
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A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation

2008 Human Molecular Genetics
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The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy

2005 Journal of Medical Genetics
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Microcephalic osteodysplastic primordial short stature type II with café-au-lait spots and moyamoya disease: Another patient

2004 American Journal of Medical Genetics Part A
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Mutation Analysis and Embryonic Expression of the HLXB9 Currarino Syndrome Gene

2000 American Journal of Human Genetics
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Mutational analysis indicates that the hereditary sacral agenesis gene, HLXB9, i s the sole locus for Currarino Triad and different mutation classes produce equivalent phenotypes.

2000
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A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

1998 American Journal of Human Genetics
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Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?

1993 American Journal of Medical Genetics
- Dian Donnai
- Margaret Barrow
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Citations (68)