Osteoarthritis? Try asporin.
- Published in:
- 2005
- By:
- Publication type:
- Other
Works matching IS 00099163 AND DT 2005 AND VI 67 AND IP 5
Results: 18
1
2
Reproductive decision making before and after predictive testing for Huntington's disease: an Australian perspective.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 404, doi. 10.1111/j.1399-0004.2005.00428.x
- By:
- Publication type:
- Article
3
Mental retardation, keratoconus, febrile seizures and sinoatrial block: a previously undescribed autosomal recessive disorder.
- Published in:
- 2005
- By:
- Publication type:
- Letter
4
Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in theSLC26A4gene in siblings.
- Published in:
- 2005
- By:
- Publication type:
- Letter
5
Looping out links Rett syndrome with loss of imprinting error.
- Published in:
- 2005
- By:
- Publication type:
- Other
6
The molecular basis of variation in human color vision.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 369, doi. 10.1111/j.1399-0004.2004.00343.x
- By:
- Publication type:
- Article
7
Is osseous dysplasia a primary feature of neurofibromatosis 1 (NF1)?
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 378, doi. 10.1111/j.1399-0004.2005.00410.x
- By:
- Publication type:
- Article
8
HJVgene mutations in European patients with juvenile hemochromatosis.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 425, doi. 10.1111/j.1399-0004.2005.00413.x
- By:
- Publication type:
- Article
9
X-linked adrenoleukodystrophy in Spain. Identification of 26 novel mutations in theABCD1gene in 80 patients. Improvement of genetic counseling in 162 relative females.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 418, doi. 10.1111/j.1399-0004.2005.00423.x
- By:
- Publication type:
- Article
10
Calibration of 6q subtelomere deletions to define genotype/phenotype correlations.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 396, doi. 10.1111/j.1399-0004.2005.00424.x
- By:
- Publication type:
- Article
11
Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 412, doi. 10.1111/j.1399-0004.2005.00425.x
- By:
- Publication type:
- Article
12
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter.
- Published in:
- 2005
- By:
- Publication type:
- Letter
13
Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 5, p. 429, doi. 10.1111/j.1399-0004.2005.00431.x
- By:
- Publication type:
- Article
14
X-linked myotubular myopathy: mutation R69C identified in a family with multiple neonatal deaths.
- Published in:
- 2005
- By:
- Publication type:
- Letter
15
TPH2: an answer for unipolar depression?
- Published in:
- 2005
- By:
- Publication type:
- Other
16
Identification and molecular characterization of 18 novel mutations in theATP7Bgene from Indian Wilson disease patients: genotype.
- Published in:
- 2005
- By:
- Publication type:
- Letter
17
Skewed X-inactivation in a family with mental retardation and PQBP1 gene mutation.
- Published in:
- 2005
- By:
- Publication type:
- Letter
18
Corrigendum.
- Published in:
- 2005
- Publication type:
- Correction Notice