1.

Characterization of a dopamine transporter polymorphism and behavior in Belgian Malinois

2.

Characterization of a dopamine transporter polymorphism and behavior in Belgian Malinois

3.

Characterization of a dopamine transporter polymorphism and behavior in Belgian Malinois

1.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

2.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

3.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

4.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

5.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

6.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

7.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

8.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

9.

Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs

1.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

2.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

3.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

4.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

5.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

6.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

7.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

8.

Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study

1.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

2.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

3.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

4.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

5.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

6.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

7.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

8.

Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres

1.

Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium

1.

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

1.

Attitudes towards predictive testing in Huntington's disease: a recent survey in Belgium.

1.

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

2.

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

3.

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

4.

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients

1.

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

2.

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

3.

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

4.

Low penetrance of a SDHB mutation in a large Dutch paraganglioma family

1.

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations?

2.

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations?

3.

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations?

4.

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations?