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Publications by K P Burdon
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
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a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
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A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome
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Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
A Novel P20R Mutation in the Alpha-B Crystallin Gene Causes Autosomal Dominant Congenital Posterior Polar Cataracts in a Chinese Family
BMC Ophthalmology
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A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease
Clinical Journal of the American Society of Nephrology
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Critical Care
Transplantation
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A Novel Heterozygous Mutation in Cardiac Calsequestrin Causes Autosomal Dominant Catecholaminergic Polymorphic Ventricular Tachycardia
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INPP5K Variant Causes Autosomal Recessive Congenital Cataract in a Pakistani Family
Clinical Genetics
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Risk Counselling in Autosomal Dominant Disorders With Undetermined Penetrance.
Journal of Medical Genetics
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Mutation in the Connexin 50 Gene (GJA8) in a Russian Family With Zonular Pulverulent Cataract
Clinical Genetics
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A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
