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Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions. [electronic resource] by
- Martin, K
- Iyengar, S
- Kalyan, A
- Lan, C
- Simon, A L
- Stosic, M
- Kobara, K
- Ravi, H
- Truong, T
- Ryan, A
- Demko, Z P
- Benn, P
Producer: 20190730
In:
Clinical genetics vol. 93
Availability: No items available.
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Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNA. [electronic resource] by
- McKanna, T
- Ryan, A
- Krinshpun, S
- Kareht, S
- Marchand, K
- Grabarits, C
- Ali, M
- McElheny, A
- Gardiner, K
- LeChien, K
- Hsu, M
- Saltzman, D
- Stosic, M
- Martin, K
- Benn, P
Producer: 20190123
In:
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 53
Availability: No items available.
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Gender-related differences in MS: a study of conventional and nonconventional MRI measures. [electronic resource] by
- Antulov, R
- Weinstock-Guttman, B
- Cox, J L
- Hussein, S
- Durfee, J
- Caiola, C
- Dwyer, M G
- Bergsland, N
- Abdelrahman, N
- Stosic, M
- Hojnacki, D
- Munschauer, F E
- Miletic, D
- Zivadinov, R
Producer: 20090522
In:
Multiple sclerosis (Houndmills, Basingstoke, England) vol. 15
Availability: No items available.
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Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome. [electronic resource] by
- Gross, S J
- Stosic, M
- McDonald-McGinn, D M
- Bassett, A S
- Norvez, A
- Dhamankar, R
- Kobara, K
- Kirkizlar, E
- Zimmermann, B
- Wayham, N
- Babiarz, J E
- Ryan, A
- Jinnett, K N
- Demko, Z
- Benn, P
Producer: 20161031
In:
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 47
Availability: No items available.
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