Works matching IS 00099163 AND DT 1974 AND VI 5 AND IP 1
Results: 13
The Roberts syndrome.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 1, doi. 10.1111/j.1399-0004.1974.tb01652.x
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- Article
Genetic and clinical relevance of haemoglobins screening: Results from a survey in a paediatric hospital.
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- Clinical Genetics, 1974, v. 5, n. 1, p. 31, doi. 10.1111/j.1399-0004.1974.tb01655.x
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- Article
A Meckel-like syndrome?
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 46, doi. 10.1111/j.1399-0004.1974.tb01658.x
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- Article
Accurate identification of the human Y chromosome.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 17, doi. 10.1111/j.1399-0004.1974.tb01653.x
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- Article
ABO blood groups and Australia antigen.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 28, doi. 10.1111/j.1399-0004.1974.tb01654.x
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- Article
Total finger ridge count and 45, X mosaicism (with and without Y chromosome).
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 68, doi. 10.1111/j.1399-0004.1974.tb01662.x
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- Article
Immunological studies in ataxia-telangiectasia.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 40, doi. 10.1111/j.1399-0004.1974.tb01657.x
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- Article
Hereditary dextrocardia associated with other congenital heart defects: Report of a pedigree.
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- Clinical Genetics, 1974, v. 5, n. 1, p. 51, doi. 10.1111/j.1399-0004.1974.tb01659.x
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- Article
Complex five-break rearrangement.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 62, doi. 10.1111/j.1399-0004.1974.tb01661.x
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- Article
The neck in the XO and XX/XO mosaic Turner's syndrome.
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- Clinical Genetics, 1974, v. 5, n. 1, p. 77, doi. 10.1111/j.1399-0004.1974.tb01664.x
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- Article
Lack of chromosomal damaging effects by moderate doses of LSD in vivo.
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- Clinical Genetics, 1974, v. 5, n. 1, p. 59, doi. 10.1111/j.1399-0004.1974.tb01660.x
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- Article
Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution.
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- Clinical Genetics, 1974, v. 5, n. 1, p. 72, doi. 10.1111/j.1399-0004.1974.tb01663.x
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- Article
Corneal opacity, microphthalmia, mental retardation, microcephaly and generaIized muscular spasticity associated with hypergIycinemia.
- Published in:
- Clinical Genetics, 1974, v. 5, n. 1, p. 36, doi. 10.1111/j.1399-0004.1974.tb01656.x
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- Article