Human embryo and early fetus research.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 98, doi. 10.1111/j.1399-0004.2006.00640.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2006 AND VI 70 AND IP 2
Results: 16
1
2
Cleidocranial dysplasia in a Polish population: high frequency of the R193X mutation.
- Published in:
- 2006
- By:
- Publication type:
- Letter
3
Farnesyl transferase inhibitors: the ‘fountain of youth’ for progeria syndromes.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 108, doi. 10.1111/j.1399-0004.2006.0645_1.x
- By:
- Publication type:
- Article
4
A role for genetics in the outcome of antidepressant treatment for major depressive disorder.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 110, doi. 10.1111/j.1399-0004.2006.0645_2.x
- By:
- Publication type:
- Article
5
A GLUT of sugar leads to a tortuous future.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 111, doi. 10.1111/j.1399-0004.2006.0645_3.x
- By:
- Publication type:
- Article
6
The genotype–phenotype correlation of hereditary multiple exostoses.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 122, doi. 10.1111/j.1399-0004.2006.00653.x
- By:
- Publication type:
- Article
7
Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 140, doi. 10.1111/j.1399-0004.2006.00647.x
- By:
- Publication type:
- Article
8
Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro.
- Published in:
- 2006
- By:
- Publication type:
- Letter
9
Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings.
- Published in:
- 2006
- By:
- Publication type:
- Letter
10
Osteogenesis imperfecta: clinical, biochemical and molecular findings.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 131, doi. 10.1111/j.1399-0004.2006.00646.x
- By:
- Publication type:
- Article
11
Phenotypic variability in isodicentric Y patients: study of nine cases.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 145, doi. 10.1111/j.1399-0004.2006.00654.x
- By:
- Publication type:
- Article
12
Neuropsychiatric findings of Möbius sequence – a review.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 91, doi. 10.1111/j.1399-0004.2006.00649.x
- By:
- Publication type:
- Article
13
Molecular and phenotypic characteristics of patients with phenylketonuria in Serbia and Montenegro.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 151, doi. 10.1111/j.1399-0004.2006.00650.x
- By:
- Publication type:
- Article
14
Microsatelite GT polymorphism in the toll-like receptor 2 is associated with colorectal cancer.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 156, doi. 10.1111/j.1399-0004.2006.00651.x
- By:
- Publication type:
- Article
15
The C-480T hepatic lipase polymorphism is associated with HDL-C but not with risk of coronary heart disease.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 114, doi. 10.1111/j.1399-0004.2006.00659.x
- By:
- Publication type:
- Article
16
Identification of novel mutations in the RSK2 gene ( RPS6KA3) in patients with Coffin–Lowry syndrome.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 2, p. 161, doi. 10.1111/j.1399-0004.2006.00660.x
- By:
- Publication type:
- Article