Paranoia in plants.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 302, doi. 10.1034/j.1399-0004.2001.590502.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2001 AND VI 59 AND IP 5
Results: 17
1
2
New Alzheimer’s disease susceptibility locus on chromosome 10q.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 303, doi. 10.1034/j.1399-0004.2001.590502.2.x
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- Publication type:
- Article
3
Transgenic monkey raises hope for primate models of human diseases.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 304, doi. 10.1034/j.1399-0004.2001.590502.3.x
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- Publication type:
- Article
4
The VACTERL association: lessons from the Sonic hedgehog pathway.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 306, doi. 10.1034/j.1399-0004.2001.590503.x
- By:
- Publication type:
- Article
5
APOC3, CETP, fibrinogen, and MTHFR are genetic determinants of carotid intima-media thickness in healthy men (the Stanislas Cohort).
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 316, doi. 10.1034/j.1399-0004.2001.590504.x
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- Publication type:
- Article
6
The risk for congenital heart defects in offspring of individuals with congenital heart defects.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 325, doi. 10.1034/j.1399-0004.2001.590505.x
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- Publication type:
- Article
7
The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 330, doi. 10.1034/j.1399-0004.2001.590506.x
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- Publication type:
- Article
8
Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfecta.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 338, doi. 10.1034/j.1399-0004.2001.590507.x
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- Publication type:
- Article
9
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 344, doi. 10.1034/j.1399-0004.2001.590508.x
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- Publication type:
- Article
10
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 350, doi. 10.1034/j.1399-0004.2001.590509.x
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- Publication type:
- Article
11
Risk factors for cataract in Chinese patients with type 2 diabetes: evidence for the influence of the aldose reductase gene.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 356, doi. 10.1034/j.1399-0004.2001.590510.x
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- Publication type:
- Article
12
Severe valvular and aortic arch calcification in a patient with Gaucher's disease homozygous for the D409H mutation.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 360, doi. 10.1034/j.1399-0004.2001.590511.x
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- Publication type:
- Article
13
Novel mutation of the Spastin gene in familial spastic paraplegia.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 364, doi. 10.1034/j.1399-0004.2001.590512.x
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- Publication type:
- Article
14
A nonsense mutation in TRPS1 in a Japanese family with tricho-rhino-phalangeal syndrome type I.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 366, doi. 10.1034/j.1399-0004.2001.590513.x
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- Publication type:
- Article
15
A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 368, doi. 10.1034/j.1399-0004.2001.590514.x
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- Publication type:
- Article
16
CYP21 mutations and congenital adrenal hyperplasia.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 293, doi. 10.1034/j.1399-0004.2001.590501.x
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- Publication type:
- Article
17
IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver–Russell syndrome.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 5, p. 371, doi. 10.1034/j.1399-0004.2001.590515.x
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- Publication type:
- Article