Syndromic and non-syndromic GLI3 phenotypes.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Works matching IS 00099163 AND DT 2005 AND VI 68 AND IP 3
Results: 18
1
2
Clinical and genetic studies in Spanish patients with Usher syndrome type II: description of new mutations and evidence for a lack of genotype–phenotype correlation.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 204, doi. 10.1111/j.1399-0004.2005.00481.x
- By:
- Publication type:
- Article
3
Response to Biesecker and Johnston.
- Published in:
- 2005
- By:
- Publication type:
- Letter
4
Psychological functioning in African American women at an increased risk of hereditary breast and ovarian cancer.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 222, doi. 10.1111/j.1399-0004.2005.00483.x
- By:
- Publication type:
- Article
5
‘Indirect’ BRCA1/2 testing. A useful approach in hereditary breast and ovarian cancer families without a living affected relative.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 228, doi. 10.1111/j.1399-0004.2005.00484.x
- By:
- Publication type:
- Article
6
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 262, doi. 10.1111/j.1399-0004.2005.00492.x
- By:
- Publication type:
- Article
7
Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000–2005.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 215, doi. 10.1111/j.1399-0004.2005.00482.x
- By:
- Publication type:
- Article
8
Sir Archibald Garrod and Alkaptonuria –‘story of metabolic genetics’.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 199, doi. 10.1111/j.1399-0004.2005.00487.x
- By:
- Publication type:
- Article
9
A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 239, doi. 10.1111/j.1399-0004.2005.00488.x
- By:
- Publication type:
- Article
10
Identification of 25 new mutations in 40 unrelated Spanish Niemann-Pick type C patients: genotype-phenotype correlations.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 245, doi. 10.1111/j.1399-0004.2005.00490.x
- By:
- Publication type:
- Article
11
An exploratory comparison of genetic counselling protocols for HNPCC predictive testing.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 255, doi. 10.1111/j.1399-0004.2005.00491.x
- By:
- Publication type:
- Article
12
Novel genomic insertion–deletion in MLH1: possible mechanistic role for non-homologous end-joining DNA repair.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 234, doi. 10.1111/j.1399-0004.2005.00486.x
- By:
- Publication type:
- Article
13
TB or not TB? Ipr1 answers the question.
- Published in:
- 2005
- By:
- Publication type:
- Other
14
Got NGF? Promising gene therapy results in Alzheimer's disease.
- Published in:
- 2005
- By:
- Publication type:
- Other
15
Silent, but deadly: epigenetic control of ID4 in leukemia.
- Published in:
- 2005
- By:
- Publication type:
- Other
16
Erratum.
- Published in:
- 2005
- Publication type:
- Correction Notice
17
Association of repeat polymorphisms in the estrogen receptors α, β, and androgen receptor genes with knee osteoarthritis.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 268, doi. 10.1111/j.1399-0004.2005.00495.x
- By:
- Publication type:
- Article
18
Copper-replacement treatment for symptomatic Menkes disease: ethical considerations.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 3, p. 278, doi. 10.1111/j.1399-0004.2005.00496.x
- By:
- Publication type:
- Article