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Association Study Between the ANF Gene and Hypertension in a Gulf Arab Population

American journal of hypertension, 1997-11, Vol.10 (11), p.1308-1310

1997

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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

Human genetics, 2003, Vol.112 (1), p.50-56

2003

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Cutaneous reactions to henna and associated additives

British journal of dermatology (1951), 1999-09, Vol.141 (3), p.598-600

1999

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Coronary heart disease in South Asia: Need to redefine risk

International journal of cardiology, 2006-02, Vol.107 (2), p.289-290

2006

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Interactions and associations of paraoxonase gene cluster polymorphisms with myocardial infarction in a Pakistani population

Clinical genetics, 2007-03, Vol.71 (3), p.238-244

2007

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Strong Association of a Renin Intronic Dimorphism with Essential Hypertension

Hypertension research, 2005-04, Vol.28 (4), p.339-344

2005

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Association of angiotensin converting enzyme gene polymorphisms with left ventricular hypertrophy

Hypertension research, 2005-04, Vol.28 (4), p.345-349

2005

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X-linked dyskeratosis congenita: restrictive pulmonary disease and a novel mutation

Thorax, 2001-11, Vol.56 (11), p.891-894

2001

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Association of G-protein beta-3 subunit gene (GNB3) T825 allele with Type II diabetes

Neuro-endocrinology letters, 2005-04, Vol.26 (2), p.87-88

2005

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R1615P: A novel mutation in ABCA1 associated with low levels of HDL and type II diabetes mellitus

International journal of cardiology, 2006-06, Vol.110 (2), p.259-260

2006

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Association of the angiotensin-converting enzyme (ACE) gene G2350A dimorphism with essential hypertension

Journal of human hypertension, 2003-10, Vol.17 (10), p.719-723

2003

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Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic Heterogeneity

American journal of human genetics, 2001-07, Vol.69 (1), p.216-222

2001

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Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless Gene

Journal of investigative dermatology, 1999-10, Vol.113 (4), p.687-690

1999

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Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder

American journal of human genetics, 1997-07, Vol.61 (1), p.94-100

1997

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Human renin gene BglI dimorphism associated with hypertension in two independent populations

Clinical genetics, 1999-12, Vol.56 (6), p.428-433

1999

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G-protein beta-3 subunit gene 825C>T dimorphism is associated with left ventricular hypertrophy but not essential hypertension

Medical science monitor, 2005-01, Vol.11 (1), p.CR6-CR9

2005

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Xeroderma pigmentosum in four siblings with three different types of malignancies simultaneously in one

Journal of pediatric hematology/oncology, 2004-08, Vol.26 (8), p.473-475

2004

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Haplotypes of the human renin gene associated with essential hypertension and stroke

Journal of human hypertension, 2001, Vol.15 (1), p.49-55

2001

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Head and Neck Cancer Susceptibility: A Genetic Marker in the Methylenetetrahydrofolate Reductase Gene

O.R.L. Journal for oto-rhino-laryngology and its related specialties, 2004-01, Vol.66 (5), p.241-245

2004

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The geographic distribution of cystic fibrosis mutations gives clues about population origins

European journal of pediatrics, 2000-07, Vol.159 (7), p.496-499

2000

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A study of five human cytokine genes in human essential hypertension

Molecular immunology, 2002-05, Vol.38 (12), p.969-976

2002

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Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T-->G)

The European respiratory journal, 1999-01, Vol.13 (1), p.100-102

1999

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Association of an Apolipoprotein B Gene Marker With Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1999-04, Vol.33 (4), p.1052-1056

1999

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A hypothesis regarding the origin and spread of the cystic fibrosis mutation ΔF508

QJM : An International Journal of Medicine, 2000-05, Vol.93 (5), p.313-315

2000

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Apolipoprotein AI promoter variant in blood pressure determination

Clinical genetics, 2002-04, Vol.61 (4), p.314-316

2002

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Association Study Between the ANF Gene and Hypertension in a Gulf Arab Population

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

Cutaneous reactions to henna and associated additives

Coronary heart disease in South Asia: Need to redefine risk

Interactions and associations of paraoxonase gene cluster polymorphisms with myocardial infarction in a Pakistani population

Strong Association of a Renin Intronic Dimorphism with Essential Hypertension

Association of angiotensin converting enzyme gene polymorphisms with left ventricular hypertrophy

X-linked dyskeratosis congenita: restrictive pulmonary disease and a novel mutation

Association of G-protein beta-3 subunit gene (GNB3) T825 allele with Type II diabetes

R1615P: A novel mutation in ABCA1 associated with low levels of HDL and type II diabetes mellitus

Association of the angiotensin-converting enzyme (ACE) gene G2350A dimorphism with essential hypertension

Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic Heterogeneity

Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless Gene

Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder

Human renin gene BglI dimorphism associated with hypertension in two independent populations

G-protein beta-3 subunit gene 825C>T dimorphism is associated with left ventricular hypertrophy but not essential hypertension

Xeroderma pigmentosum in four siblings with three different types of malignancies simultaneously in one

Haplotypes of the human renin gene associated with essential hypertension and stroke

Head and Neck Cancer Susceptibility: A Genetic Marker in the Methylenetetrahydrofolate Reductase Gene

The geographic distribution of cystic fibrosis mutations gives clues about population origins

A study of five human cytokine genes in human essential hypertension

Genotype-phenotype correlations in cystic fibrosis: clinical severity of mutation S549R(T-->G)

Association of an Apolipoprotein B Gene Marker With Essential Hypertension

A hypothesis regarding the origin and spread of the cystic fibrosis mutation ΔF508

Apolipoprotein AI promoter variant in blood pressure determination

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