Silent microcephaly: A distinct autosomal dominant trait.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 281, doi. 10.1111/j.1399-0004.1983.tb01877.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1983 AND VI 23 AND IP 4
Results: 18
1
2
The wrinkly skin syndrome: A report of two siblings from Saudi Arabia.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 308, doi. 10.1111/j.1399-0004.1983.tb01882.x
- By:
- Publication type:
- Article
3
HLA and disease: Haplotype sharing in multiplex families.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 267, doi. 10.1111/j.1399-0004.1983.tb01875.x
- By:
- Publication type:
- Article
4
Detection of Fabry's disease heterozy. gotes by enzyme analysis in single fibroblasts after cell sorting.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 261, doi. 10.1111/j.1399-0004.1983.tb01874.x
- By:
- Publication type:
- Article
5
Reflections on muscular dystrophy in a Sudanese kindred.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 325, doi. 10.1111/j.1399-0004.1983.tb01886.x
- By:
- Publication type:
- Article
6
Tandem duplication of chromosome 14 (q24+q32) in male newborn with congenital malformations.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 321, doi. 10.1111/j.1399-0004.1983.tb01885.x
- By:
- Publication type:
- Article
7
The Rubinstein-Taybi syndrome: Occurrence in two sets of identical twins.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 318, doi. 10.1111/j.1399-0004.1983.tb01884.x
- By:
- Publication type:
- Article
8
Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome?
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 329, doi. 10.1111/j.1399-0004.1983.tb01887.x
- By:
- Publication type:
- Article
9
Letters to the Editors.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 336, doi. 10.1111/j.1399-0004.1983.tb01888.x
- By:
- Publication type:
- Article
10
Cytogenetics of recurrent abortions.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 294, doi. 10.1111/j.1399-0004.1983.tb01879.x
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- Publication type:
- Article
11
Announcements.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 339, doi. 10.1111/j.1399-0004.1983.tb01890.x
- Publication type:
- Article
12
Chronic granulomatous disease carrier geno-dermatosis (CGDCGD).
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 276, doi. 10.1111/j.1399-0004.1983.tb01876.x
- By:
- Publication type:
- Article
13
Family resemblance for fasting blood glucose in a population of Japanese Americans.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 287, doi. 10.1111/j.1399-0004.1983.tb01878.x
- By:
- Publication type:
- Article
14
Diagnosis of cystic fibrosis homozygotes and heterozygotes from plasma and fibroblast cultures. A three-generation family study.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 298, doi. 10.1111/j.1399-0004.1983.tb01880.x
- By:
- Publication type:
- Article
15
Letters to the Editors.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 338, doi. 10.1111/j.1399-0004.1983.tb01889.x
- By:
- Publication type:
- Article
16
Erratum.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 340, doi. 10.1111/j.1399-0004.1983.tb01891.x
- Publication type:
- Article
17
The fragile X chromosome in a large Indian kindred.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 311, doi. 10.1111/j.1399-0004.1983.tb01883.x
- By:
- Publication type:
- Article
18
Translocations in Prader-WiIIi syndrome.
- Published in:
- Clinical Genetics, 1983, v. 23, n. 4, p. 304, doi. 10.1111/j.1399-0004.1983.tb01881.x
- By:
- Publication type:
- Article