Genetic landmarks through philately – Charles Robert Darwin.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 270, doi. 10.1034/j.1399-0004.2001.600404.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 2001 AND VI 60 AND IP 4
Results: 15
1
2
The developmental program of the hypothalamus and its disorders.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 255, doi. 10.1034/j.1399-0004.2001.600402.x
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- Publication type:
- Article
3
Pulling roots of the thorny chorea-acanthocytosis.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 266, doi. 10.1034/j.1399-0004.2001.600403.2.x
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- Article
4
Neurodegeneration: iron weighs in.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 267, doi. 10.1034/j.1399-0004.2001.600403.3.x
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- Publication type:
- Article
5
Genetic determinants of type 2 diabetes mellitus.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 243, doi. 10.1034/j.1399-0004.2001.600401.x
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- Publication type:
- Article
6
Digesting genetic information in gastric cancers.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 4, p. 264, doi. 10.1034/j.1399-0004.2001.600403.1.x
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- Publication type:
- Article
7
Molecular basis of Mucopolysaccharidosis type II in Portugal: identification of four novel mutations.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 316, doi. 10.1034/j.1399-0004.2001.600412.x
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- Publication type:
- Article
8
Living with Marfan syndrome I. Perceptions of the condition.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 273, doi. 10.1034/j.1399-0004.2001.600405.x
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- Publication type:
- Article
9
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 293, doi. 10.1034/j.1399-0004.2001.600407.x
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- Publication type:
- Article
10
Living with Marfan syndrome II. Medication adherence and physical activity modification.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 283, doi. 10.1034/j.1399-0004.2001.600406.x
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- Publication type:
- Article
11
Waardenburg syndrome type 3 (Klein–Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?
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- Clinical Genetics, 2001, v. 60, n. 4, p. 301, doi. 10.1034/j.1399-0004.2001.600408.x
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- Publication type:
- Article
12
Real-time quantitative PCR analysis for α-thalassemia-1 of Southeast Asian type deletion in Taiwan.
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- Clinical Genetics, 2001, v. 60, n. 4, p. 305, doi. 10.1034/j.1399-0004.2001.600409.x
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- Publication type:
- Article
13
Hereditary breast/ovarian cancer – pitfalls in genetic counseling.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 4, p. 310, doi. 10.1034/j.1399-0004.2001.600410.x
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- Article
14
A de novo mutation (R279C) in theP63 gene in a patient with EEC syndrome.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 4, p. 314, doi. 10.1034/j.1399-0004.2001.600411.x
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- Publication type:
- Article
15
Effects of pravastatin therapy on serum lipids and coronary reactivity are not associated with SREBP cleavage-activating protein polymorphism in healthy young men.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 4, p. 319, doi. 10.1034/j.1399-0004.2001.600413.x
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- Publication type:
- Article