Corrigendum.
- Published in:
- 2008
- Publication type:
- Correction Notice
Works matching IS 00099163 AND DT 2008 AND VI 73 AND IP 5
Results: 19
1
2
Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 430, doi. 10.1111/j.1399-0004.2008.00978.x
- By:
- Publication type:
- Article
3
Huntington disease-like 2: the first patient with apparent European ancestry.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 480, doi. 10.1111/j.1399-0004.2008.00981.x
- By:
- Publication type:
- Article
4
Sugar coats on proteins, not always as sweet as they sound!
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 428, doi. 10.1111/j.1399-0004.2008.00990_3.x
- By:
- Publication type:
- Article
5
Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the myelin transcription factor 1 gene ( MYT1).
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 492, doi. 10.1111/j.1399-0004.2008.00982.x
- By:
- Publication type:
- Article
6
Corrigendum.
- Published in:
- 2008
- Publication type:
- Correction Notice
7
Erratum.
- Published in:
- 2008
- Publication type:
- Correction Notice
8
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 486, doi. 10.1111/j.1399-0004.2008.00969.x
- By:
- Publication type:
- Article
9
Erratum.
- Published in:
- 2008
- Publication type:
- Correction Notice
10
Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiency.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 496, doi. 10.1111/j.1399-0004.2008.00986.x
- By:
- Publication type:
- Article
11
Advances in the genetics of sarcoidosis.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 401, doi. 10.1111/j.1399-0004.2008.00970.x
- By:
- Publication type:
- Article
12
Genetic causes of chronic pancreatitis: the elucidation of genetic contributions to a disorder once thought to have none.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 424, doi. 10.1111/j.1399-0004.2008.00990_1.x
- By:
- Publication type:
- Article
13
Gene dosage imbalances in patients with 46,XY gonadal DSD detected by an in-house-designed synthetic probe set for multiplex ligation-dependent probe amplification analysis.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 453, doi. 10.1111/j.1399-0004.2008.00980.x
- By:
- Publication type:
- Article
14
Little people, big discovery.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 425, doi. 10.1111/j.1399-0004.2008.00990_2.x
- By:
- Publication type:
- Article
15
A re-examination of the chromosome 8p22-8p23.1 region in Kabuki syndrome.
- Published in:
- 2008
- By:
- Publication type:
- Letter
16
ATM germline mutations in Spanish early-onset breast cancer patients negative for BRCA1/BRCA2 mutations.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 465, doi. 10.1111/j.1399-0004.2008.00987.x
- By:
- Publication type:
- Article
17
The ups and downs of holoprosencephaly: dorsal versus ventral patterning forces.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 413, doi. 10.1111/j.1399-0004.2008.00994.x
- By:
- Publication type:
- Article
18
Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 474, doi. 10.1111/j.1399-0004.2008.00988.x
- By:
- Publication type:
- Article
19
Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease.
- Published in:
- Clinical Genetics, 2008, v. 73, n. 5, p. 441, doi. 10.1111/j.1399-0004.2008.00989.x
- By:
- Publication type:
- Article