Hartwig Cleve.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 57, doi. 10.1111/j.1399-0004.1995.tb03924.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1995 AND VI 47 AND IP 2
Results: 17
1
2
Effect of the StuI polymorphism in the LDL receptor gene (Ala 370 to Thr) on lipid levels in healthy individuals.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 68, doi. 10.1111/j.1399-0004.1995.tb03926.x
- By:
- Publication type:
- Article
3
Retinitis pigmentosa in India: a genetic and segregation analysis.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 75, doi. 10.1111/j.1399-0004.1995.tb03927.x
- By:
- Publication type:
- Article
4
Premature thelarche in Möbius syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 108, doi. 10.1111/j.1399-0004.1995.tb03938.x
- By:
- Publication type:
- Article
5
Psychosocial and sexual functioning in women with Turner syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 85, doi. 10.1111/j.1399-0004.1995.tb03929.x
- By:
- Publication type:
- Article
6
Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolism.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 59, doi. 10.1111/j.1399-0004.1995.tb03925.x
- By:
- Publication type:
- Article
7
Familial mental retardation and progressive spasticity.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 107, doi. 10.1111/j.1399-0004.1995.tb03936.x
- By:
- Publication type:
- Article
8
Phenotypic heterogeneity in CF sibs compound heterozygous for the G85E and 621 + 1G→T mutations.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 110, doi. 10.1111/j.1399-0004.1995.tb03939.x
- By:
- Publication type:
- Article
9
A BamHI polymorphism in the human cytochrome P450 gene, CYP2D6.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 103, doi. 10.1111/j.1399-0004.1995.tb03934.x
- By:
- Publication type:
- Article
10
Mild cystic fibrosis disease in three Mexican delta-F508/G551S compound heterozygous siblings.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 96, doi. 10.1111/j.1399-0004.1995.tb03931.x
- By:
- Publication type:
- Article
11
Congenital cardiac malformations in Adams-Oliver syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 80, doi. 10.1111/j.1399-0004.1995.tb03928.x
- By:
- Publication type:
- Article
12
Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein ( PLP) gene.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 99, doi. 10.1111/j.1399-0004.1995.tb03932.x
- By:
- Publication type:
- Article
13
Reply.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 107, doi. 10.1111/j.1399-0004.1995.tb03937.x
- By:
- Publication type:
- Article
14
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 90, doi. 10.1111/j.1399-0004.1995.tb03930.x
- By:
- Publication type:
- Article
15
A rare silent G to T mutation in exon 4 of the human low density lipoprotein receptor gene.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 101, doi. 10.1111/j.1399-0004.1995.tb03933.x
- By:
- Publication type:
- Article
16
An informative Hindlll polymorphism associated with the βB1 crystallin gene (CRYBB1) on human chromosome 22.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 105, doi. 10.1111/j.1399-0004.1995.tb03935.x
- By:
- Publication type:
- Article
17
Announcements.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 2, p. 112, doi. 10.1111/j.1399-0004.1995.tb03940.x
- Publication type:
- Article