Identification of heterozygotes for glycogenosis 2 (Acid maltase deficiency).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 55, doi. 10.1111/j.1399-0004.1981.tb00668.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1981 AND VI 19 AND IP 1
Results: 16
1
2
In utero diagnosis of achondrogenesis, type I.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 51, doi. 10.1111/j.1399-0004.1981.tb00667.x
- By:
- Publication type:
- Article
3
Automatic chromosome analysis.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 26, doi. 10.1111/j.1399-0004.1981.tb00663.x
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- Publication type:
- Article
4
Trisomy 3 mosaicism in a live-born infant.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 37, doi. 10.1111/j.1399-0004.1981.tb00664.x
- By:
- Publication type:
- Article
5
Familial sex chromosome mosaicism (yes) and interchromosomal effects (no).
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 77, doi. 10.1111/j.1399-0004.1981.tb00673.x
- By:
- Publication type:
- Article
6
Slowly progressive autosomal dominant spastic paraplegia with late onset, variable expression and reduced penetrance: a basis for diagnosis and counseling.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 1, doi. 10.1111/j.1399-0004.1981.tb00659.x
- By:
- Publication type:
- Article
7
Roberts's syndrome.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 71, doi. 10.1111/j.1399-0004.1981.tb00671.x
- By:
- Publication type:
- Article
8
Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 64, doi. 10.1111/j.1399-0004.1981.tb00669.x
- By:
- Publication type:
- Article
9
Incidence of major chromosomal abnormalities.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 75, doi. 10.1111/j.1399-0004.1981.tb00672.x
- By:
- Publication type:
- Article
10
Familial additional chromosomal fragment ascertained in amniotic cell culture.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 46, doi. 10.1111/j.1399-0004.1981.tb00666.x
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- Publication type:
- Article
11
International Conference on Dermatoglyphics.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 79, doi. 10.1111/j.1399-0004.1981.tb00674.x
- Publication type:
- Article
12
Abnormality of chromosome 16 and its phenotypic expression.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 41, doi. 10.1111/j.1399-0004.1981.tb00665.x
- By:
- Publication type:
- Article
13
Spondylocostal dysostosis in South African sisters.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 23, doi. 10.1111/j.1399-0004.1981.tb00662.x
- By:
- Publication type:
- Article
14
Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 8, doi. 10.1111/j.1399-0004.1981.tb00660.x
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- Publication type:
- Article
15
Prenatal diagnosis of Gaucher disease Assay of the ß-glucosidase activity in amniotic fluid cells cultivated in two laboratories with different cultivation conditions.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 16, doi. 10.1111/j.1399-0004.1981.tb00661.x
- By:
- Publication type:
- Article
16
Apparent influence of marker genotypes on variation in serum cholesterol in monozygotic twins.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 1, p. 67, doi. 10.1111/j.1399-0004.1981.tb00670.x
- By:
- Publication type:
- Article