Works matching IS 00099163 AND DT 1986 AND VI 30 AND IP 1
Results: 11
Number of 'high genes' involved in determining the activity of paraoxonase.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 41, doi. 10.1111/j.1399-0004.1986.tb00567.x
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- Publication type:
- Article
Structure, origin and effects of a supernumerary marker chromosome 15.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 63, doi. 10.1111/j.1399-0004.1986.tb00570.x
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- Publication type:
- Article
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriers.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 38, doi. 10.1111/j.1399-0004.1986.tb00566.x
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- Publication type:
- Article
An unusual variant chromosome 9 due to disturbance of normal chromatin condensation at band p12?
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 80, doi. 10.1111/j.1399-0004.1986.tb00573.x
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- Publication type:
- Article
Normal female carrier and affected male half-sibs with t (X;5) (q13;p15).
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 59, doi. 10.1111/j.1399-0004.1986.tb00569.x
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- Publication type:
- Article
Partial trisomy 3p syndrome.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 50, doi. 10.1111/j.1399-0004.1986.tb00568.x
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- Publication type:
- Article
Autosomal whole arm translocations in man.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 72, doi. 10.1111/j.1399-0004.1986.tb00571.x
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- Publication type:
- Article
Usher syndrome in four Norwegian counties.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 14, doi. 10.1111/j.1399-0004.1986.tb00564.x
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- Publication type:
- Article
Paternal non-disjunction in a 46, XY/ 47, XXY individual with a fragile 17p12 in the mother.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 76, doi. 10.1111/j.1399-0004.1986.tb00572.x
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- Publication type:
- Article
Adult polycystic liver and kidney diseases are separate entities.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 29, doi. 10.1111/j.1399-0004.1986.tb00565.x
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- Publication type:
- Article
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 1, p. 1, doi. 10.1111/j.1399-0004.1986.tb00563.x
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- Publication type:
- Article