Erratum.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 421, doi. 10.1111/j.1399-0004.1982.tb01400.x
- Publication type:
- Article
Works matching IS 00099163 AND DT 1982 AND VI 21 AND IP 6
Results: 14
1
2
Serum reserve cholesterol binding capacity (SRCBC) in familial hypercholesterolemia.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 362, doi. 10.1111/j.1399-0004.1982.tb01388.x
- By:
- Publication type:
- Article
3
Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel-Manzke syndrome. A case report and review of the literature.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 407, doi. 10.1111/j.1399-0004.1982.tb01395.x
- By:
- Publication type:
- Article
4
Association of genotype and total cholesterol in MZ twins.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 418, doi. 10.1111/j.1399-0004.1982.tb01397.x
- By:
- Publication type:
- Article
5
X-chromosomes attached by their long arm: case report and replication kinetics of the rearranged X-chromosome.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 384, doi. 10.1111/j.1399-0004.1982.tb01392.x
- By:
- Publication type:
- Article
6
Mucopolysaccharidosis type VII (β-glucuronidase deficiency): a report of a new case and a survey of those in the literature.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 366, doi. 10.1111/j.1399-0004.1982.tb01389.x
- By:
- Publication type:
- Article
7
Hyperexplexia: an inherited disorder of the startle response.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 388, doi. 10.1111/j.1399-0004.1982.tb01393.x
- By:
- Publication type:
- Article
8
The Fifth Annual Symposium on Genetics for Practicing Physicians September 12, 1982.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 420, doi. 10.1111/j.1399-0004.1982.tb01398.x
- Publication type:
- Article
9
Symposium.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 420, doi. 10.1111/j.1399-0004.1982.tb01399.x
- Publication type:
- Article
10
Increased amniotic alphafetoprotein due to a holoacardium amorphous twin.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 382, doi. 10.1111/j.1399-0004.1982.tb01391.x
- By:
- Publication type:
- Article
11
Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 357, doi. 10.1111/j.1399-0004.1982.tb01387.x
- By:
- Publication type:
- Article
12
Supernumerary chromosomes in six patients.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 397, doi. 10.1111/j.1399-0004.1982.tb01394.x
- By:
- Publication type:
- Article
13
Quantitative identification of banded human chromosomes.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 411, doi. 10.1111/j.1399-0004.1982.tb01396.x
- By:
- Publication type:
- Article
14
Catalytically defective ganglioside neuraminidase in mucolipidosis IV.
- Published in:
- Clinical Genetics, 1982, v. 21, n. 6, p. 374, doi. 10.1111/j.1399-0004.1982.tb01390.x
- By:
- Publication type:
- Article