Works matching IS 00099163 AND DT 1982 AND VI 22 AND IP 4
Results: 11
Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man.
- Published in:
- Clinical Genetics, 1982, v. 22, n. 4, p. 180, doi. 10.1111/j.1399-0004.1982.tb01432.x
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- Article
The distribution of clinical findings in Bechterew's syndrome (ankylosing spondylitis) suggests distinct genetic subgroups.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 151, doi. 10.1111/j.1399-0004.1982.tb01428.x
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- Article
Fronto-metaphyseaI dysplasia. Further delineation of the clinical syndrome.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 195, doi. 10.1111/j.1399-0004.1982.tb01433.x
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- Article
Further evidence by gene dosage for the regional assignment of erythrocyte acid phosphatase (ACPI) and malate dehydrogenase (MDHI) loci on chromosome 2p.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 220, doi. 10.1111/j.1399-0004.1982.tb01437.x
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- Article
Familial ectrodactyly and polydactyly: variable expressivity of one single gene - embryological considerations.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 206, doi. 10.1111/j.1399-0004.1982.tb01434.x
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- Article
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 172, doi. 10.1111/j.1399-0004.1982.tb01431.x
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- Article
Impaired degradation of chondroitin sulfate in GM.
- Published in:
- Clinical Genetics, 1982, v. 22, n. 4, p. 165, doi. 10.1111/j.1399-0004.1982.tb01430.x
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- Article
Copper/zinc superoxide dismutase (SOD-1) activity in regular trisomy 21, trisomy 21 by translocation and mosaic trisomy 21.
- Published in:
- Clinical Genetics, 1982, v. 22, n. 4, p. 160, doi. 10.1111/j.1399-0004.1982.tb01429.x
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- Article
Ornithine transcarbamylase deficiency: long-term survival.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 211, doi. 10.1111/j.1399-0004.1982.tb01435.x
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- Article
Interstitial deletion of chromosome 21.
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- Clinical Genetics, 1982, v. 22, n. 4, p. 215, doi. 10.1111/j.1399-0004.1982.tb01436.x
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- Article
Interstitial de novo deletion of the long arm of chromosome 5: Mapping of 5q bands associated with particular malformations.
- Published in:
- Clinical Genetics, 1982, v. 22, n. 4, p. 226, doi. 10.1111/j.1399-0004.1982.tb01438.x
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- Publication type:
- Article