| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Advances in fetal echocardiography
|
Gardiner, Helena M.
|
|
2018
|
23 |
2 |
p. 112-118
|
artikel
|
| 2 |
Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing
|
Hayward, Jane
|
|
2018
|
23 |
2 |
p. 94-101
|
artikel
|
| 3 |
Carrier screening for single gene disorders
|
Rose, Nancy C.
|
|
2018
|
23 |
2 |
p. 78-84
|
artikel
|
| 4 |
Editorial Board
|
|
|
2018
|
23 |
2 |
p. ii
|
artikel
|
| 5 |
First and second trimester screening for fetal structural anomalies
|
Edwards, Lindsay
|
|
2018
|
23 |
2 |
p. 102-111
|
artikel
|
| 6 |
Genetic counselling, patient education, and informed decision-making in the genomic era
|
Metcalfe, Sylvia A.
|
|
2018
|
23 |
2 |
p. 142-149
|
artikel
|
| 7 |
[No title]
|
Kumar, Rohit
|
|
2018
|
23 |
2 |
p. 155
|
artikel
|
| 8 |
Parental experiences after prenatal diagnosis of fetal abnormality
|
Hodgson, Jan
|
|
2018
|
23 |
2 |
p. 150-154
|
artikel
|
| 9 |
Prenatal screening for fetal and obstetric complications: New opportunities and challenges
|
Vora, Neeta L.
|
|
2018
|
23 |
2 |
p. 77
|
artikel
|
| 10 |
Screening for fetal chromosomal and subchromosomal disorders
|
Harris, Sarah
|
|
2018
|
23 |
2 |
p. 85-93
|
artikel
|
| 11 |
Screening for fetal growth restriction and placental insufficiency
|
Audette, Melanie C.
|
|
2018
|
23 |
2 |
p. 119-125
|
artikel
|
| 12 |
Screening for spontaneous preterm birth and resultant therapies to reduce neonatal morbidity and mortality: A review
|
Glover, Angelica V.
|
|
2018
|
23 |
2 |
p. 126-132
|
artikel
|
| 13 |
Ultrasound screening for complications in twin pregnancy
|
Townsend, Rosemary
|
|
2018
|
23 |
2 |
p. 133-141
|
artikel
|
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