Huntington disease carrier status and the problems involved for those affected. A psychotherapeutic experience.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 172, doi. 10.1111/j.1399-0004.1988.tb02858.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1988 AND VI 34 AND IP 3
Results: 13
1
2
Fibroblasts of two patients with trisomy 18 show 1.5-fold increase in peptidase A activity over normal human diploid fibroblasts.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 161, doi. 10.1111/j.1399-0004.1988.tb02856.x
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- Publication type:
- Article
3
Ring chromosome 22 46,XX,r(22)(p11.2→q13.3) presenting with leukemoid reaction.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 206, doi. 10.1111/j.1399-0004.1988.tb02865.x
- By:
- Publication type:
- Article
4
Defective polymorphonuclear chemotaxis in patients with Turner's.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 165, doi. 10.1111/j.1399-0004.1988.tb02857.x
- By:
- Publication type:
- Article
5
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic Republic.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 176, doi. 10.1111/j.1399-0004.1988.tb02859.x
- By:
- Publication type:
- Article
6
Four copies of 8p in a mentally retarded boy with the mosaic karyotype 47,XY, +i(8p)/46,XY.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 201, doi. 10.1111/j.1399-0004.1988.tb02863.x
- By:
- Publication type:
- Article
7
Familial occurrence of isodicentric X chromosomes with different breakpoints.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 153, doi. 10.1111/j.1399-0004.1988.tb02855.x
- By:
- Publication type:
- Article
8
False negative findings at third trimester chorionic villus sampling (C.V.S.).
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 204, doi. 10.1111/j.1399-0004.1988.tb02864.x
- By:
- Publication type:
- Article
9
Risk effect of maternal age in Pallister i(12p) syndrome.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 181, doi. 10.1111/j.1399-0004.1988.tb02860.x
- By:
- Publication type:
- Article
10
Child neuromuscular disease in Southern Norway: Prevalence, age and distribution of diagnosis with special reference to 'non-Duchenne muscular dystrophy'.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 145, doi. 10.1111/j.1399-0004.1988.tb02854.x
- By:
- Publication type:
- Article
11
Acid α-neuraminidase deficiency: a nephropathic phenotype?
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 185, doi. 10.1111/j.1399-0004.1988.tb02861.x
- By:
- Publication type:
- Article
12
The origin of isochromosomes.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 207, doi. 10.1111/j.1399-0004.1988.tb02866.x
- By:
- Publication type:
- Article
13
A new family with the Townes-Brocks syndrome.
- Published in:
- Clinical Genetics, 1988, v. 34, n. 3, p. 195, doi. 10.1111/j.1399-0004.1988.tb02862.x
- By:
- Publication type:
- Article