Clinical teratology: identifying teratogenic risks in humans.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 409, doi. 10.1034/j.1399-0004.1999.560601.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1999 AND VI 56 AND IP 6
Results: 15
1
2
Genetic landmarks through philately - Henry Louis 'Lou' Gehrig and amyotrophic lateral sclerosis.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 425, doi. 10.1034/j.1399-0004.1999.560603.x
- Publication type:
- Article
3
Unmasking mutations: functional genetic testing.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 421, doi. 10.1034/j.1399-0004.1999.560602.x
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- Publication type:
- Article
4
Human renin gene BglI dimorphism associated with hypertension in two independent populations.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 428, doi. 10.1034/j.1399-0004.1999.560604.x
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- Publication type:
- Article
5
Epigenetic evidence: hypomethylation results in hypermutation.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 423, doi. 10.1034/j.1399-0004.1999.5606022.x
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- Publication type:
- Article
6
Molecular recipe for a human tumour.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 422, doi. 10.1034/j.1399-0004.1999.5606021.x
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- Publication type:
- Article
7
Perceptions of the outcome of orthopedic surgery in patients with chondrodysplasias.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 434, doi. 10.1034/j.1399-0004.1999.560605.x
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- Publication type:
- Article
8
Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 441, doi. 10.1034/j.1399-0004.1999.560606.x
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- Publication type:
- Article
9
Relation of mathematical ability to psychosis in Iceland.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 447, doi. 10.1034/j.1399-0004.1999.560607.x
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- Publication type:
- Article
10
Prevalence of human leukocyte antigen DQA1 and DQB1 alleles in Kuwaiti Arab children with type 1 diabetes mellitus.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 450, doi. 10.1034/j.1399-0004.1999.560608.x
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- Publication type:
- Article
11
Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMM.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 457, doi. 10.1034/j.1399-0004.1999.560609.x
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- Publication type:
- Article
12
Postaxial polydactyly and Dandy–Walker malformation. Further nosological comments.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 462, doi. 10.1034/j.1399-0004.1999.560610.x
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- Publication type:
- Article
13
Search for uniparental disomy 14 in balanced Robertsonian translocation carriers.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 464, doi. 10.1034/j.1399-0004.1999.560611.x
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- Publication type:
- Article
14
Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 467, doi. 10.1034/j.1399-0004.1999.560612.x
- By:
- Publication type:
- Article
15
A de novo heterozygous deletion of 42 base-pairs in the noggin gene of afibrodysplasia ossificansprogressiva patient.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 6, p. 469, doi. 10.1034/j.1399-0004.1999.560613.x
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- Publication type:
- Article