Goals of genetic counseling.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 323, doi. 10.1034/j.1399-0004.2001.600501.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2001 AND VI 60 AND IP 5
Results: 18
1
2
Right place-right time; real time protein–protein interactions.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 331, doi. 10.1034/j.1399-0004.2001.6005021.x
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- Publication type:
- Article
3
Shutting off mammalian gene expression the easy way.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 332, doi. 10.1034/j.1399-0004.2001.6005022.x
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- Publication type:
- Article
4
Genetic studies yield conflicting data in schizophrenia.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 333, doi. 10.1034/j.1399-0004.2001.6005023.x
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- Publication type:
- Article
5
Tandem duplication mosaicism: characterization of a mosaic dup(5q) and review.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 366, doi. 10.1034/j.1399-0004.2001.600508.x
- By:
- Publication type:
- Article
6
Familial deletion of (8)(q24.13q24.22) associated with a normal phenotype.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 371, doi. 10.1034/j.1399-0004.2001.600509.x
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- Publication type:
- Article
7
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotype.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 336, doi. 10.1034/j.1399-0004.2001.600503.x
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- Publication type:
- Article
8
Familial case of Potocki–Shaffer syndrome associated with microdeletion of EXT2 and ALX4.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 356, doi. 10.1034/j.1399-0004.2001.600506.x
- By:
- Publication type:
- Article
9
Evaluation for sleep apnea in patients with Ehlers–Danlos syndrome and Marfan: a questionnaire study.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 360, doi. 10.1034/j.1399-0004.2001.600507.x
- By:
- Publication type:
- Article
10
Association of a single nucleotide polymorphism in CPB2 encoding the thrombin-activable fibrinolysis inhibitor (TAFI) with blood pressure.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 345, doi. 10.1034/j.1399-0004.2001.600504.x
- By:
- Publication type:
- Article
11
A PCR-based method for detecting known mutations in the human UDP galactose-4′-epimerase gene associated with epimerase-deficiency galactosemia.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 350, doi. 10.1034/j.1399-0004.2001.600505.x
- By:
- Publication type:
- Article
12
Lack of association of the common TaqIB polymorphism in the cholesteryl ester transfer protein gene with angiographically assessed coronary atherosclerosis.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 374, doi. 10.1034/j.1399-0004.2001.600510.x
- By:
- Publication type:
- Article
13
Apolipoproteins AI, B, and E polymorphisms in severe aortic valve stenosis.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 381, doi. 10.1034/j.1399-0004.2001.600511.x
- By:
- Publication type:
- Article
14
PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 385, doi. 10.1034/j.1399-0004.2001.600512.x
- By:
- Publication type:
- Article
15
The frequency of common mutations among patients with mucopolysaccharidosis types I, II and IIIA diagnosed in Austria over the last 17 years.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 393, doi. 10.1034/j.1399-0004.2001.600513.x
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- Publication type:
- Article
16
Segmental uniparental disomy of 7q31-qter is rare in Silver–Russell syndrome.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 395, doi. 10.1034/j.1399-0004.2001.600514.x
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- Publication type:
- Article
17
‘The VACTERL association: lessons from the Sonic hedgehog pathway’.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 397, doi. 10.1034/j.1399-0004.2001.600515.x
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- Publication type:
- Article
18
A Reply.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 5, p. 398, doi. 10.1034/j.1399-0004.2001.600516.x
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- Publication type:
- Article