Found: 14
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Linkage analysis in von Willebrand disease.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 434, doi. 10.1111/j.1399-0004.1983.tb00099.x
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- Publication type:
- Article
Prader-Willi syndrome associated with inversion of chromosome 15.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 456, doi. 10.1111/j.1399-0004.1983.tb00104.x
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- Publication type:
- Article
Fragile X syndrome in mildly mentally retarded children in a Northern Swedish county. A prevalence study.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 393, doi. 10.1111/j.1399-0004.1983.tb00092.x
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- Article
Letter to the Editors.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 462, doi. 10.1111/j.1399-0004.1983.tb00105.x
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- Publication type:
- Article
The femur, fibula, ulna (FFU) complex in siblings.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 449, doi. 10.1111/j.1399-0004.1983.tb00102.x
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- Publication type:
- Article
Genetic regulation of the red cell uroporphyrinogen-l-synthetase level in families with acute intermittent porphyria.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 403, doi. 10.1111/j.1399-0004.1983.tb00094.x
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- Publication type:
- Article
Additional data on spontaneous abortion and facial cleft malformations.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 407, doi. 10.1111/j.1399-0004.1983.tb00095.x
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- Publication type:
- Article
The relevance of pre-amniocentesis pedigree analysis and genetic counseling.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 429, doi. 10.1111/j.1399-0004.1983.tb00098.x
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- Publication type:
- Article
Y chromosome length related to fetal loss.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 413, doi. 10.1111/j.1399-0004.1983.tb00096.x
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- Publication type:
- Article
Genetic regulation of melatonin excretion in urine.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 399, doi. 10.1111/j.1399-0004.1983.tb00093.x
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- Publication type:
- Article
Association between the degree of mosaicism and the severity of syndrome in Turner mosaics and Klinefelter mosaics.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 420, doi. 10.1111/j.1399-0004.1983.tb00097.x
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- Publication type:
- Article
Silver-Russell syndrome with absence of digits and syndactylism of the fingers.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 453, doi. 10.1111/j.1399-0004.1983.tb00103.x
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- Publication type:
- Article
The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 439, doi. 10.1111/j.1399-0004.1983.tb00100.x
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- Publication type:
- Article
Male to male transmission of the G syndrome.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 6, p. 446, doi. 10.1111/j.1399-0004.1983.tb00101.x
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- Publication type:
- Article