Angiotensinogen genotype, plasma protein and mRNA concentration in isolated systolic hypertension.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 363, doi. 10.1034/j.1399-0004.2002.610508.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 2002 AND VI 61 AND IP 5
Results: 15
1
2
Inherited hypertrichoses.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 321, doi. 10.1034/j.1399-0004.2002.610501.x
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- Publication type:
- Article
3
Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 335, doi. 10.1034/j.1399-0004.2002.610503.x
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- Publication type:
- Article
4
HotSpots.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 330, doi. 10.1034/j.1399-0004.2002.610502.x
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- Publication type:
- Article
5
Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 380, doi. 10.1034/j.1399-0004.2002.610511.x
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- Publication type:
- Article
6
Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 344, doi. 10.1046/j.0009-9163.2002.00251.x
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- Publication type:
- Article
7
New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 349, doi. 10.1034/j.1399-0004.2002.610505.x
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- Publication type:
- Article
8
Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 354, doi. 10.1034/j.1399-0004.2002.610506.x
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- Publication type:
- Article
9
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 359, doi. 10.1034/j.1399-0004.2002.610507.x
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- Publication type:
- Article
10
A patient homozygous for the SCA6 gene with retinitis pigmentosa.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 375, doi. 10.1034/j.1399-0004.2002.610510.x
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- Publication type:
- Article
11
Familial lethal skeletal dysplasia with cloverleaf skull and multiple anomalies of brain, eye, face and heart: a new autosomal recessive multiple congenital anomalies syndrome.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 369, doi. 10.1034/j.1399-0004.2002.610509.x
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- Publication type:
- Article
12
MECP2 mutations in Swedish Rett syndrome clusters.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 384, doi. 10.1034/j.1399-0004.2002.610512.x
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- Publication type:
- Article
13
Familial pericentric inversion of chromosome 4: inv(4)(p16.1q12).
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 386, doi. 10.1034/j.1399-0004.2002.610513.x
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- Publication type:
- Article
14
High prevalence of I179S mutation in patients with late-onset metachromatic leukodystrophy.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 389, doi. 10.1034/j.1399-0004.2002.610514.x
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- Publication type:
- Article
15
Early development of megarectum in myotonic dystrophy.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 5, p. 391, doi. 10.1034/j.1399-0004.2002.610515.x
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- Publication type:
- Article