scholarly article | Q13442814 |
P2093 | author name string | Macri JN | |
Krantz DA | |||
Hallahan TW | |||
Macri VJ | |||
P2860 | cites work | Screening for Down syndrome using first-trimester combined screening followed by second-trimester ultrasound examination in an unselected population | Q58416056 |
P433 | issue | 6 | |
P921 | main subject | Down syndrome | Q47715 |
P304 | page(s) | 666-670 | |
P577 | publication date | 2007-06-01 | |
P1433 | published in | Ultrasound in Obstetrics and Gynecology | Q1817048 |
P1476 | title | Genetic sonography after first-trimester Down syndrome screening | |
P478 | volume | 29 |
Q46618495 | Agenesis of ductus venosus in sequential first and second trimester screening |
Q51501850 | Contribution of "modified genetic sonography" to the combined test as a screening method for chromosomal abnormalities. |
Q36308492 | First and second trimester serum tests with and without first trimester ultrasound tests for Down's syndrome screening. |
Q24187589 | First trimester serum tests for Down's syndrome screening |
Q36308489 | First trimester ultrasound tests alone or in combination with first trimester serum tests for Down's syndrome screening |
Q36848484 | Noninvasive screening tools for Down syndrome: a review |
Q60054137 | Prenatal diagnosis and pregnancy outcome analysis of thickened nuchal fold in the second trimester |
Q37322448 | Prenatal diagnosis: update on invasive versus noninvasive fetal diagnostic testing from maternal blood |
Q84836506 | Prenatal testing for Down syndrome: comparison of screening practices in the UK and USA |
Q51376807 | Role of fetal echocardiography in stepwise sequential screening for chromosomal disorders (combined test associated with modified genetic sonography). |
Q36776424 | Role of second-trimester genetic sonography after Down syndrome screening |
Q38179321 | Role of the second-trimester 'genetic sonogram' for Down syndrome screen in the era of first-trimester screening and noninvasive prenatal testing |
Q43424745 | What is the importance of second-trimester "soft markers" for trisomy 21 after an 11- to 14-week aneuploidy screening scan? |