Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 163, doi. 10.1111/j.1399-0004.1984.tb00479.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1984 AND VI 25 AND IP 2
Results: 17
1
2
Letters to the Editors.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 219, doi. 10.1111/j.1399-0004.1984.tb00489.x
- By:
- Publication type:
- Article
3
Ring chromosome 10 syndrome: case report and the possibility of clinical diagnosis.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 196, doi. 10.1111/j.1399-0004.1984.tb00485.x
- By:
- Publication type:
- Article
4
Letters to the Editors.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 214, doi. 10.1111/j.1399-0004.1984.tb00488.x
- By:
- Publication type:
- Article
5
Marker chromosomes in parents to children with Down's syndrome.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 140, doi. 10.1111/j.1399-0004.1984.tb00476.x
- By:
- Publication type:
- Article
6
Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patients.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 191, doi. 10.1111/j.1399-0004.1984.tb00484.x
- By:
- Publication type:
- Article
7
Diagnostic considerations in arthrogry-posis syndromes in South Africa.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 155, doi. 10.1111/j.1399-0004.1984.tb00478.x
- By:
- Publication type:
- Article
8
Bloom's syndrome XI. Progress report for 1983.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 166, doi. 10.1111/j.1399-0004.1984.tb00480.x
- By:
- Publication type:
- Article
9
Familial minor neurodevelopmental disorders.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 148, doi. 10.1111/j.1399-0004.1984.tb00477.x
- By:
- Publication type:
- Article
10
Polymorphism of the human Y chromosome: the evaluation of the correlation between the DNA content and the size of the heterochromatin and euchromatin.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 125, doi. 10.1111/j.1399-0004.1984.tb00473.x
- By:
- Publication type:
- Article
11
A new psychomotor retardation syndrome with peculiar facies and marfan-oid habitus.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 187, doi. 10.1111/j.1399-0004.1984.tb00483.x
- By:
- Publication type:
- Article
12
The NEU-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 201, doi. 10.1111/j.1399-0004.1984.tb00486.x
- By:
- Publication type:
- Article
13
Clinical and Genetic Aspects of Fanconi's Anaemia Abstracts from Workshop at Free University.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 205, doi. 10.1111/j.1399-0004.1984.tb00487.x
- Publication type:
- Article
14
The psychological profile of the fragile X syndrome.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 131, doi. 10.1111/j.1399-0004.1984.tb00474.x
- By:
- Publication type:
- Article
15
Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 182, doi. 10.1111/j.1399-0004.1984.tb00482.x
- By:
- Publication type:
- Article
16
In vitro reversal of fragile-X expression by exogenous thymidine.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 135, doi. 10.1111/j.1399-0004.1984.tb00475.x
- By:
- Publication type:
- Article
17
The syndromic status of sclerosteosis and van Buchem disease.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 2, p. 175, doi. 10.1111/j.1399-0004.1984.tb00481.x
- By:
- Publication type:
- Article