nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
CME Accreditation Page
|
|
|
|
52 |
3 |
p. xiii-xiv |
artikel |
2 |
Contents
|
|
|
|
52 |
3 |
p. vii-x |
artikel |
3 |
Contributors
|
|
|
|
52 |
3 |
p. iii-vi |
artikel |
4 |
Copyright
|
|
|
|
52 |
3 |
p. ii |
artikel |
5 |
Cystic Fibrosis Newborn Screening
|
Shenoy, Ambika |
|
|
52 |
3 |
p. 477-493 |
artikel |
6 |
Early Hearing Detection
|
Findlen, Ursula M. |
|
|
52 |
3 |
p. 509-521 |
artikel |
7 |
Forthcoming Issues
|
|
|
|
52 |
3 |
p. xi |
artikel |
8 |
Genetics, Newborn Screening, and Inborn Errors of Metabolism
|
Gallagher, Patrick G. |
|
|
52 |
3 |
p. i |
artikel |
9 |
Genetics of Congenital Heart Disease
|
Yasuhara, Jun |
|
|
52 |
3 |
p. 589-608 |
artikel |
10 |
Genetic Testing in the Neonate
|
D’Gama, Alissa M. |
|
|
52 |
3 |
p. 575-588 |
artikel |
11 |
Newborn Pulse-Oximetry Screening
|
Kumar, Harish |
|
|
52 |
3 |
p. 539-554 |
artikel |
12 |
Newborn Screening: Advances, Challenges, and Future Directions
|
Ben-Moshe, Yishay |
|
|
52 |
3 |
p. 449-459 |
artikel |
13 |
Newborn Screening and Perinatal Genetic Diagnostic Testing
|
Gallagher, Patrick G. |
|
|
52 |
3 |
p. xvii-xix |
artikel |
14 |
Newborn Screening for Hemoglobin Disorders
|
Therrell, Bradford L. |
|
|
52 |
3 |
p. 461-476 |
artikel |
15 |
Newborn Screening of the Endocrine System
|
Blew, Kathryn |
|
|
52 |
3 |
p. 495-508 |
artikel |
16 |
Newborn Screening: The Time Is Now
|
Jain, Lucky |
|
|
52 |
3 |
p. xv-xvi |
artikel |
17 |
Prenatal Genetic Diagnosis
|
Hamilton, Jameaka Latrice |
|
|
52 |
3 |
p. 555-574 |
artikel |
18 |
The Case for Universal Newborn Congenital Cytomegalovirus Screening
|
Sánchez, Sarah M. |
|
|
52 |
3 |
p. 523-538 |
artikel |
19 |
The Emerging Role of Genome Sequencing in Newborn Screening
|
Chaudhari, Bimal P. |
|
|
52 |
3 |
p. 609-628 |
artikel |