| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ACMG Genetics Review Course
|
|
|
|
7 |
3 |
p. 216-217
|
artikel
|
| 2 |
Ariadne Genomics Announces the Release of Seqware Data Center Self-Updating Sequence Data Management and Personal Blast System
|
|
|
|
7 |
3 |
p. 219-220
|
artikel
|
| 3 |
Carrier screening panels for Ashkenazi Jews: Is more better?
|
Leib, Jennifer R.
|
|
|
7 |
3 |
p. 185-190
|
artikel
|
| 4 |
Frequency and phenotypic consequences of the 3199del6 CFTR mutation in French Canadians
|
Ruchon, Andrea Frota
|
|
|
7 |
3 |
p. 210-211
|
artikel
|
| 5 |
Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension
|
Cogan, Joy D.
|
|
|
7 |
3 |
p. 169-174
|
artikel
|
| 6 |
Health implications of α1-antitrypsin deficiency in Sub-Sahara African countries and their emigrants in Europe and the New World
|
de Serres, Frederick J.
|
|
|
7 |
3 |
p. 175-184
|
artikel
|
| 7 |
HFE gene mutations in susceptibility to childhood leukemia: HuGE review
|
Te Dorak, M vfik
|
|
|
7 |
3 |
p. 159-168
|
artikel
|
| 8 |
Impact of direct-to-consumer advertising for hereditary breast cancer testing on genetic services at a managed care organization: A naturally-occurring experiment
|
Mouchawar, Judy
|
|
|
7 |
3 |
p. 191-197
|
artikel
|
| 9 |
Is the IVS2+4T>C variant of the HFE gene a splicing mutation or a polymorphism? A study in the Spanish population
|
de Lucas, Arantza Pacho
|
|
|
7 |
3 |
p. 212-213
|
artikel
|
| 10 |
Meetings Calendar
|
|
|
|
7 |
3 |
p. 218
|
artikel
|
| 11 |
Neonatal screening, clinical features and genetic testing for galactosemia
|
Zaffanello, Marco
|
|
|
7 |
3 |
p. 211-212
|
artikel
|
| 12 |
Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci
|
Brisson, Diane
|
|
|
7 |
3 |
p. 213-215
|
artikel
|
| 13 |
Qualitative research: Thoughts on how to do it; how to judge it; when to use it
|
Press, Nancy
|
|
|
7 |
3 |
p. 155-158
|
artikel
|
| 14 |
Response to Drs. Herring and Grundmann
|
Marazita, Mary L.
|
|
|
7 |
3 |
p. 209-210
|
artikel
|
| 15 |
Scientists' and science writers' experiences reporting genetic discoveries: Toward an ethic of trust in science journalism
|
Geller, Gail
|
|
|
7 |
3 |
p. 198-205
|
artikel
|
| 16 |
Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms
|
Capaccio, P
|
|
|
7 |
3 |
p. 206-208
|
artikel
|
| 17 |
The IRF6 p.274V polymorphism is not a risk factor for isolated cleft lip
|
Hering, Robert
|
|
|
7 |
3 |
p. 209
|
artikel
|
Tijdschrift beschrijving