Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 427, doi. 10.1111/j.1399-0004.1997.tb02563.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1997 AND VI 52 AND IP 6
Results: 8
1
2
Discordance between malignant hyperthermia susceptibility and RYR1 mutation C1840T in two Scandinavian MH families exhibiting this mutation.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 416, doi. 10.1111/j.1399-0004.1997.tb02561.x
- By:
- Publication type:
- Article
3
Cardiovascular risk factors in people with different genotypes in the insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme (ACE).
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 422, doi. 10.1111/j.1399-0004.1997.tb02562.x
- By:
- Publication type:
- Article
4
Words of Thanks.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 415, doi. 10.1111/j.1399-0004.1997.tb02560.x
- By:
- Publication type:
- Article
5
Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, + r(X).
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 432, doi. 10.1111/j.1399-0004.1997.tb02564.x
- By:
- Publication type:
- Article
6
Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 436, doi. 10.1111/j.1399-0004.1997.tb02565.x
- By:
- Publication type:
- Article
7
Case Report: Partial trisomy of 15q due to inserted inverted duplication.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 442, doi. 10.1111/j.1399-0004.1997.tb02566.x
- By:
- Publication type:
- Article
8
Variant euchromatic band within 16q12.1.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 6, p. 446, doi. 10.1111/j.1399-0004.1997.tb02567.x
- By:
- Publication type:
- Article