Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 335, doi. 10.1111/j.1399-0004.1987.tb03298.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1987 AND VI 32 AND IP 5
Results: 11
1
2
New type of spinocerebellar degeneration syndrome in a northern Swedish population.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 306, doi. 10.1111/j.1399-0004.1987.tb03295.x
- By:
- Publication type:
- Article
3
A rapid and efficient screening method for DNA restriction fragment length polymorphisms.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 349, doi. 10.1111/j.1399-0004.1987.tb03300.x
- By:
- Publication type:
- Article
4
Homozygous variegate porphyria A severe skin disease of Infancy.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 300, doi. 10.1111/j.1399-0004.1987.tb03294.x
- By:
- Publication type:
- Article
5
A new autosomal dominant craniofacial deafness syndrome.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 355, doi. 10.1111/j.1399-0004.1987.tb03301.x
- By:
- Publication type:
- Article
6
X-linked dysmorphic syndrome with mental retardation.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 326, doi. 10.1111/j.1399-0004.1987.tb03297.x
- By:
- Publication type:
- Article
7
Linkage of G8 (D4S10) in two Swedish families with Huntington's disease.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 289, doi. 10.1111/j.1399-0004.1987.tb03292.x
- By:
- Publication type:
- Article
8
Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 295, doi. 10.1111/j.1399-0004.1987.tb03293.x
- By:
- Publication type:
- Article
9
X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 360, doi. 10.1111/j.1399-0004.1987.tb03302.x
- By:
- Publication type:
- Article
10
Free proximal trisomy 21 without the Down syndrome.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 342, doi. 10.1111/j.1399-0004.1987.tb03299.x
- By:
- Publication type:
- Article
11
Progressive mental regression in siblings with Morquio disease Type B (mucopolysaccharidosis IV B).
- Published in:
- Clinical Genetics, 1987, v. 32, n. 5, p. 313, doi. 10.1111/j.1399-0004.1987.tb03296.x
- By:
- Publication type:
- Article