Prior abortions and neural tube defects.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 201, doi. 10.1111/j.1399-0004.1980.tb00872.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1980 AND VI 18 AND IP 3
Results: 16
1
2
Abnormalities of sexual differentiation in campomelic dwarfs.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 223, doi. 10.1111/j.1399-0004.1980.tb00876.x
- By:
- Publication type:
- Article
3
Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset corrections.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 160, doi. 10.1111/j.1399-0004.1980.tb00864.x
- By:
- Publication type:
- Article
4
Guadalajara camptodactyly syndrome.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 153, doi. 10.1111/j.1399-0004.1980.tb00863.x
- By:
- Publication type:
- Article
5
HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 197, doi. 10.1111/j.1399-0004.1980.tb00871.x
- By:
- Publication type:
- Article
6
Genetic counselling for adult polycystic kidney disease. Ultrasound a useful tool in pre-symptomatic diagnosis?
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 168, doi. 10.1111/j.1399-0004.1980.tb00865.x
- By:
- Publication type:
- Article
7
Familial occurrence of intracranial arterial occlusive disease (Moyamoya) in neurofibromatosis.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 191, doi. 10.1111/j.1399-0004.1980.tb00870.x
- By:
- Publication type:
- Article
8
A modified method for the identification of heterozygotes for Gaucher's disease using differential thermal inactivation.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 226, doi. 10.1111/j.1399-0004.1980.tb00877.x
- By:
- Publication type:
- Article
9
Chlorpropamide-alcohol flushing is not useful for individual genetic counseling of diabetic patients.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 189, doi. 10.1111/j.1399-0004.1980.tb00869.x
- By:
- Publication type:
- Article
10
Announcements.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 232, doi. 10.1111/j.1399-0004.1980.tb00878.x
- Publication type:
- Article
11
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 203, doi. 10.1111/j.1399-0004.1980.tb00873.x
- By:
- Publication type:
- Article
12
Dominantly inherited macular degeneration (Best's disease) in a homozygous father with 11 children.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 211, doi. 10.1111/j.1399-0004.1980.tb00874.x
- By:
- Publication type:
- Article
13
Familial Williams Syndrome.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 173, doi. 10.1111/j.1399-0004.1980.tb00866.x
- By:
- Publication type:
- Article
14
Addison disease and cerebral sclerosis in an apparently heterozygous girl: evidence for inactivation of the adrenoleukodystrophy locus.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 184, doi. 10.1111/j.1399-0004.1980.tb00868.x
- By:
- Publication type:
- Article
15
Pitfalls in the prenatal diagnosis of propionic acidemia.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 177, doi. 10.1111/j.1399-0004.1980.tb00867.x
- By:
- Publication type:
- Article
16
Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 3, p. 217, doi. 10.1111/j.1399-0004.1980.tb00875.x
- By:
- Publication type:
- Article