Osteogenesis imperfecta or Osteoporosis-pseudoglioma syndrome.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 447, doi. 10.1111/j.1399-0004.1986.tb01907.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1986 AND VI 30 AND IP 5
Results: 17
1
2
Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45, X/ 46, XY fetus with testes.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 366, doi. 10.1111/j.1399-0004.1986.tb01893.x
- By:
- Publication type:
- Article
3
The acrocallosal syndrome in sisters.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 399, doi. 10.1111/j.1399-0004.1986.tb01897.x
- By:
- Publication type:
- Article
4
A postaxial Polydactyly and progressive myopia syndrome of autosomal dominant origin.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 406, doi. 10.1111/j.1399-0004.1986.tb01898.x
- By:
- Publication type:
- Article
5
Concerning the article 'Gonadoblastoma and Y chromosome fluorescence'. Clin. Genet. 29, 311-316 (1986).
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 446, doi. 10.1111/j.1399-0004.1986.tb01906.x
- By:
- Publication type:
- Article
6
P
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 428, doi. 10.1111/j.1399-0004.1986.tb01902.x
- By:
- Publication type:
- Article
7
Triplication, Partial Tetrasomy or Tetramere?
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 445, doi. 10.1111/j.1399-0004.1986.tb01905.x
- By:
- Publication type:
- Article
8
Spastic paresis, glaucoma and mental retardation - a probable autosomal recessive syndrome?
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 416, doi. 10.1111/j.1399-0004.1986.tb01900.x
- By:
- Publication type:
- Article
9
A new chromosome instability disorder.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 353, doi. 10.1111/j.1399-0004.1986.tb01892.x
- By:
- Publication type:
- Article
10
Multiple sulphatase deficiency presenting at birth.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 409, doi. 10.1111/j.1399-0004.1986.tb01899.x
- By:
- Publication type:
- Article
11
Exencephaly in human fetuses.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 440, doi. 10.1111/j.1399-0004.1986.tb01904.x
- By:
- Publication type:
- Article
12
A racial difference in apolipoprotein E allele frequencies between the Japanese and Caucasian populations.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 422, doi. 10.1111/j.1399-0004.1986.tb01901.x
- By:
- Publication type:
- Article
13
The problem of isolated cases of Huntington's disease in South Wales 1974-1984.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 433, doi. 10.1111/j.1399-0004.1986.tb01903.x
- By:
- Publication type:
- Article
14
Dominantly inherited craniodiaphyseal dysplasia: A new craniotubular dysplasia.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 381, doi. 10.1111/j.1399-0004.1986.tb01895.x
- By:
- Publication type:
- Article
15
Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 392, doi. 10.1111/j.1399-0004.1986.tb01896.x
- By:
- Publication type:
- Article
16
The CHARGE syndrome.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 448, doi. 10.1111/j.1399-0004.1986.tb01908.x
- By:
- Publication type:
- Article
17
Mental retardation in a North Swedish isolate.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 5, p. 374, doi. 10.1111/j.1399-0004.1986.tb01894.x
- By:
- Publication type:
- Article