Corrigendum.
- Published in:
- 2007
- Publication type:
- Correction Notice
Works matching IS 00099163 AND DT 2007 AND VI 71 AND IP 1
Results: 17
1
2
The genetics of hydatidiform moles: new lights on an ancient disease.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 25, doi. 10.1111/j.1399-0004.2006.00697.x
- By:
- Publication type:
- Article
3
The modular nature of genetic diseases.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 1, doi. 10.1111/j.1399-0004.2006.00708.x
- By:
- Publication type:
- Article
4
Diagnosis and management of early- and late-onset cerebellar ataxia.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 12, doi. 10.1111/j.1399-0004.2006.00722.x
- By:
- Publication type:
- Article
5
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1.
- Published in:
- 2007
- By:
- Publication type:
- Letter
6
Overlapping clinical phenotypes: the road to identifying dysmorphology signalling pathways and their associated risks.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 43, doi. 10.1111/j.1399-0004.2006.00726_1.x
- By:
- Publication type:
- Article
7
The neoplastic risk in children with Noonan syndrome and Costello syndrome.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 44, doi. 10.1111/j.1399-0004.2006.00726_2.x
- By:
- Publication type:
- Article
8
Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost-effectiveness of testing algorithms.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 46, doi. 10.1111/j.1399-0004.2006.00727.x
- By:
- Publication type:
- Article
9
In search of a familial cancer risk assessment tool.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 76, doi. 10.1111/j.1399-0004.2006.00728.x
- By:
- Publication type:
- Article
10
Six novel mutations in the GCK gene in MODY patients.
- Published in:
- 2007
- By:
- Publication type:
- Letter
11
Prevalence of C282Y, H63D and S65C mutations of the hemochromatosis ( HFE) gene in a population from southeastern Spain (Murcia Region).
- Published in:
- 2007
- By:
- Publication type:
- Letter
12
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 35, doi. 10.1111/j.1399-0004.2007.00731.x
- By:
- Publication type:
- Article
13
The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 59, doi. 10.1111/j.1399-0004.2007.00732.x
- By:
- Publication type:
- Article
14
Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 84, doi. 10.1111/j.1399-0004.2007.00733.x
- By:
- Publication type:
- Article
15
ENG mutations in MADH4/BMPR1A mutation negative patients with juvenile polyposis.
- Published in:
- 2007
- By:
- Publication type:
- Letter
16
Early lethal autosomal recessive enterocolitis: report of a second family.
- Published in:
- 2007
- By:
- Publication type:
- Letter
17
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.
- Published in:
- Clinical Genetics, 2007, v. 71, n. 1, p. 67, doi. 10.1111/j.1399-0004.2007.00736.x
- By:
- Publication type:
- Article