Short Report Association of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 433, doi. 10.1034/j.1399-0004.2003.00148.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2003 AND VI 64 AND IP 5
Results: 15
1
2
Genetic epidemiology of alpha-1 antitrypsin deficiency in North America and Australia/New Zealand: Australia, Canada, New Zealand and the United States of America.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 382, doi. 10.1034/j.1399-0004.2003.00143.x
- By:
- Publication type:
- Article
3
Letter to the Editor Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome).
- Published in:
- 2003
- By:
- Publication type:
- Letter
4
Short Report A−61C and C−101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 439, doi. 10.1034/j.1399-0004.2003.00149.x
- By:
- Publication type:
- Article
5
Short Report Peroxisome proliferator-activated receptor γ C161T polymorphisms and survival of Japanese patients with immunoglobulin A nephropathy.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 398, doi. 10.1034/j.1399-0004.2003.00154.x
- By:
- Publication type:
- Article
6
Short Report Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler–Najjar syndrome type I and Gilbert's syndrome.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 420, doi. 10.1034/j.1399-0004.2003.00136.x
- By:
- Publication type:
- Article
7
Short Report Omphalocele in trisomy 3q: further delineation of phenotype.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 404, doi. 10.1034/j.1399-0004.2003.00159.x
- By:
- Publication type:
- Article
8
Short Report Genetic variation in the promoter and 5′ UTR of the copper transporter, ATP7B, in patients with Wilson disease.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 429, doi. 10.1034/j.1399-0004.2003.00160.x
- By:
- Publication type:
- Article
9
Short Report Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 424, doi. 10.1034/j.1399-0004.2003.00161.x
- By:
- Publication type:
- Article
10
Short Report FH-Pyrgos: a novel mutation in the promoter (−45delT) of the low-density lipoprotein receptor gene associated with familial hypercholesterolemia.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 5, p. 414, doi. 10.1034/j.1399-0004.2003.00164.x
- By:
- Publication type:
- Article
11
HotSpot Mutations in components of the dynein motor protein complex cause motor neuron disease.
- Published in:
- 2003
- By:
- Publication type:
- Other
12
HotSpot Mechanism-specific treatment of a polyglutamine disorder.
- Published in:
- 2003
- By:
- Publication type:
- Other
13
HotSpot Do these genes make me look fat? Obesity and melanocortin-4 receptor gene deficiencies.
- Published in:
- 2003
- By:
- Publication type:
- Other
14
Letter to the Editor Hemochromatosis gene mutations in the Croatian and Slovenian populations.
- Published in:
- 2003
- By:
- Publication type:
- Letter
15
Erratum.
- Published in:
- 2003
- Publication type:
- Correction Notice