nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
College News
|
|
|
|
7 |
8 |
p. 591-592 |
artikel |
2 |
Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: Assessment of anxiety, depression, and perception of health
|
Patch, Christine |
|
|
7 |
8 |
p. 550-556 |
artikel |
3 |
Developing a Sustainable Process to Provide Quality Control Materials for Genetic Testing
|
Chen, Bin |
|
|
7 |
8 |
p. 534-549 |
artikel |
4 |
Economic analyses of human genetics services: A systematic review
|
Carlson, Josh J. |
|
|
7 |
8 |
p. 519-523 |
artikel |
5 |
Fragile X syndrome: Diagnostic and carrier testing
|
Sherman, Stephanie |
|
|
7 |
8 |
p. 584-587 |
artikel |
6 |
In Defense of Commercial Laboratories
|
Strom, Charles |
|
|
7 |
8 |
p. 590 |
artikel |
7 |
Letter: Peas, Priorities and Primary Care: Cultural competency starts at home.
|
Feero, W Gregory |
|
|
7 |
8 |
p. 588-589 |
artikel |
8 |
Newborn blood spot screening and genetic services: A survey of Minnesota primary care physicians
|
Thompson, Diane B. |
|
|
7 |
8 |
p. 564-570 |
artikel |
9 |
NSD1 analysis for Sotos syndrome: Insights and perspectives from the clinical laboratory
|
Waggoner, Darrel J. |
|
|
7 |
8 |
p. 524-533 |
artikel |
10 |
Patient acceptability of genotypic testing for hemochromatosis in primary care
|
Anderson, Roger T. |
|
|
7 |
8 |
p. 557-563 |
artikel |
11 |
Technical Standards and Guidelines: Molecular Genetic Testing for Ultra-Rare Disorders
|
Maddalena, Anne |
|
|
7 |
8 |
p. 571-583 |
artikel |