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Blood levels of kynurenines, interleukin-23 and soluble human leucocyte antigen-G at different stages of Huntington's disease

Journal of neurochemistry, 2010, Vol.112 (1), p.112-122

2010

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Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome

BMC genomics, 2005-03, Vol.6 (1), p.38-38, Article 38

2005

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A further patient with Noonan syndrome due to a SOS1 mutation and rhabdomyosarcoma

Genes chromosomes & cancer, 2010-10, Vol.49 (10), p.967-968

2010

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Double-labelling immunohistochemistry for MGMT and a "cocktail" of non-tumourous elements is a reliable, quick and easy technique for inferring methylation status in glioblastomas and other primary brain tumours

Acta neuropathologica communications, 2013-06, Vol.1 (1), p.22-22, Article 22

2013

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FLT 4 / VEGFR 3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Human mutation, 2013-01, Vol.34 (1), p.23-31

2013

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Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy

Journal of medical genetics, 2000-09, Vol.37 (9), p.e18-18

2000

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Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene

Human genetics, 1999-12, Vol.105 (6), p.648-653

1999

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Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction

British Heart Journal, 1992-12, Vol.68 (12), p.554-559

1992

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Huntington's disease: a molecular genetic and CT comparison

Journal of neurology, neurosurgery and psychiatry, 1996-02, Vol.60 (2), p.206-208

1996

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An unusual variant detected using a ?-globin probe for an individual with the sickle cell trait

Human genetics, 1991-09, Vol.87 (5)

1991

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RESOLUTION, BY DNA PROBES, OF UNCERTAIN DIAGNOSIS OF INHERITANCE OF HYPERCHOLESTEROLAEMIA

The Lancet (British edition), 1988-10, Vol.332 (8614), p.794-795

1988

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Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female

Journal of medical genetics, 1991-09, Vol.28 (9), p.591-595

1991

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A further patient with Noonan syndrome due to a SOS1 mutation and rhabdomyosarcoma

Genes, chromosomes & cancer, 2010, Vol.49 (10), p.967-968

2010

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An unusual variant detected using a β-globin probe for an individual with the sickle cell trait

Human genetics, 1991-09, Vol.87 (5), p.631-631

1991

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A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration

Human genetics, 1988-03, Vol.78 (3), p.237-239

1988

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Recombinant DNA technology and low-density lipoprotein receptor defects

Biochemical Society transactions, 1987-04, Vol.15 (2), p.202-203

1987

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Muzio Clementi and British Musical Culture: Sources, Performance Practice and Style

1st, 2019

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Prenatal diagnosis and the subsequent mutation analysis in a family with carbohydrate-deficient glycoprotein type I syndrome: growing evidence to support founder effects within CDG1 populations

Genetic testing, 1999-01, Vol.3 (3), p.305-307

1999

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Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversion

Genetic testing, 2000, Vol.4 (4), p.365-370

2000

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Nutritional and Metabolic Derangements in Pancreatic Cancer and Pancreatic Resection

Nutrients, 2017-03, Vol.9 (3), p.243

2017

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Deregressing estimated breeding values and weighting information for genomic regression analyses

Genetics selection evolution (Paris), 2009-12, Vol.41 (1), p.55-55, Article 55

2009

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Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction

British heart journal, 1992-12, Vol.68 (6), p.554-559

1992

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Illicit Finance and the Law in the Commonwealth Caribbean: The Myth of Paradise

Clarke, Rohan D

1, 2022

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COVID-19 Pandemic: The Threat and Response

1, 2022

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Blood levels of kynurenines, interleukin-23 and soluble human leucocyte antigen-G at different stages of Huntington's disease

Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome

A further patient with Noonan syndrome due to a SOS1 mutation and rhabdomyosarcoma

Double-labelling immunohistochemistry for MGMT and a "cocktail" of non-tumourous elements is a reliable, quick and easy technique for inferring methylation status in glioblastomas and other primary brain tumours

FLT 4 / VEGFR 3 and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy

Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene

Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction

Huntington's disease: a molecular genetic and CT comparison

An unusual variant detected using a ?-globin probe for an individual with the sickle cell trait

RESOLUTION, BY DNA PROBES, OF UNCERTAIN DIAGNOSIS OF INHERITANCE OF HYPERCHOLESTEROLAEMIA

Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories

Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female

A further patient with Noonan syndrome due to a SOS1 mutation and rhabdomyosarcoma

An unusual variant detected using a β-globin probe for an individual with the sickle cell trait

A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration

Recombinant DNA technology and low-density lipoprotein receptor defects

Muzio Clementi and British Musical Culture: Sources, Performance Practice and Style

Prenatal diagnosis and the subsequent mutation analysis in a family with carbohydrate-deficient glycoprotein type I syndrome: growing evidence to support founder effects within CDG1 populations

Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversion

Nutritional and Metabolic Derangements in Pancreatic Cancer and Pancreatic Resection

Deregressing estimated breeding values and weighting information for genomic regression analyses

Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction

Illicit Finance and the Law in the Commonwealth Caribbean: The Myth of Paradise

COVID-19 Pandemic: The Threat and Response

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