Works matching IS 00099163 AND DT 1984 AND VI 25 AND IP 2
Results: 17
Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 163, doi. 10.1111/j.1399-0004.1984.tb00479.x
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- Article
Letters to the Editors.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 219, doi. 10.1111/j.1399-0004.1984.tb00489.x
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- Article
Ring chromosome 10 syndrome: case report and the possibility of clinical diagnosis.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 196, doi. 10.1111/j.1399-0004.1984.tb00485.x
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- Article
Letters to the Editors.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 214, doi. 10.1111/j.1399-0004.1984.tb00488.x
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- Article
Marker chromosomes in parents to children with Down's syndrome.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 140, doi. 10.1111/j.1399-0004.1984.tb00476.x
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- Article
Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patients.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 191, doi. 10.1111/j.1399-0004.1984.tb00484.x
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- Article
Diagnostic considerations in arthrogry-posis syndromes in South Africa.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 155, doi. 10.1111/j.1399-0004.1984.tb00478.x
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- Article
Bloom's syndrome XI. Progress report for 1983.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 166, doi. 10.1111/j.1399-0004.1984.tb00480.x
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- Article
Familial minor neurodevelopmental disorders.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 148, doi. 10.1111/j.1399-0004.1984.tb00477.x
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- Article
Polymorphism of the human Y chromosome: the evaluation of the correlation between the DNA content and the size of the heterochromatin and euchromatin.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 125, doi. 10.1111/j.1399-0004.1984.tb00473.x
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- Article
A new psychomotor retardation syndrome with peculiar facies and marfan-oid habitus.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 187, doi. 10.1111/j.1399-0004.1984.tb00483.x
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- Article
The NEU-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 201, doi. 10.1111/j.1399-0004.1984.tb00486.x
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- Article
Clinical and Genetic Aspects of Fanconi's Anaemia Abstracts from Workshop at Free University.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 205, doi. 10.1111/j.1399-0004.1984.tb00487.x
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- Article
The psychological profile of the fragile X syndrome.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 131, doi. 10.1111/j.1399-0004.1984.tb00474.x
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- Article
Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 182, doi. 10.1111/j.1399-0004.1984.tb00482.x
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- Article
In vitro reversal of fragile-X expression by exogenous thymidine.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 135, doi. 10.1111/j.1399-0004.1984.tb00475.x
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- Article
The syndromic status of sclerosteosis and van Buchem disease.
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- Clinical Genetics, 1984, v. 25, n. 2, p. 175, doi. 10.1111/j.1399-0004.1984.tb00481.x
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- Article