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Author/Creator Stosic, M.

1. Clinical experience with a single‐nucleotide polymorphism‐based non‐invasive prenatal test for five clinically significant microdeletions. Issue 2 (17th November 2017)

Authors:
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.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 2(2018)
Page Start:
293
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome. (5th January 2016)

Authors:
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.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 47:Number 2(2016)
Page Start:
177
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. 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. (26th November 2018)

Authors:
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.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 53:Number 1(2019)
Page Start:
73
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗