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Studwell, Courtney
16
results:
Search for persons
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Format
Online (16)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (6)
Sorted by: Relevance
Sorted by: Year
?
1
Postnatal genetic testing on cord blood for prenatally iden..:
Adams, Sophie
;
Llorin, Hannah
;
Dobson, Lori J.
...
Prenatal Diagnosis. 43 (2023) 9 - p. 1120-1131 , 2023
Link:
https://doi.org/10.1002/..
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2
Genetic counseling for fetal sex prediction by NIPT: Challe..:
Stevens, Chelsea
;
Llorin, Hannah
;
Gabriel, Camila
...
Journal of Genetic Counseling. 32 (2023) 5 - p. 945-956 , 2023
Link:
https://doi.org/10.1002/..
?
3
O39: Comprehensive, high-resolution, and non-invasive prena..:
Duyzend, Michael
;
Brand, Harrison
;
Whelan, Christopher
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100646 , 2023
Link:
https://doi.org/10.1016/..
?
4
Chromosomal microarray analysis in pregnancy loss: Is it ti..:
Schilit, Samantha L. P.
;
Studwell, Courtney
;
Flatley, Pamela
...
Prenatal Diagnosis. 42 (2022) 12 - p. 1545-1553 , 2022
Link:
https://doi.org/10.1002/..
?
5
eP395: Calculating recurrence risk in an individual with an..:
Schilit, Samantha
;
Bell, Avery
;
Rowsey, Ross
...
Genetics in Medicine. 24 (2022) 3 - p. S248-S249 , 2022
Link:
https://doi.org/10.1016/..
?
6
Rare disease patient matchmaking: development and outcomes ..:
LeBlanc, Kimberly
;
Glanton, Emily
;
Nagy, Anna
...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
7
Utility of noninvasive genome-wide screening: a prospective..:
Guseh, Stephanie
;
Wilkins-Haug, Louise
;
Kaimal, Anjali
...
Genetics in Medicine. 23 (2021) 7 - p. 1341-1348 , 2021
Link:
https://doi.org/10.1038/..
?
8
Chromosomal microarray testing of products of conception ti..:
Schilit, Samantha
;
Studwell, Courtney
;
Flatley, Pamela
...
Molecular Genetics and Metabolism. 132 (2021) - p. S310 , 2021
Link:
https://doi.org/10.1016/..
?
9
Rural distribution of human papilloma virus in low- and mid..:
Atkinson, Aaron
;
Studwell, Courtney
;
Bejarano, Suyapa
...
Experimental and Molecular Pathology. 104 (2018) 2 - p. 146-150 , 2018
Link:
https://doi.org/10.1016/..
?
10
Family genetic result communication in rare and undiagnosed..:
Studwell, Courtney M.
;
Kelley, Emily G.
;
Sinsheimer, Janet S.
...
Journal of Genetic Counseling. 30 (2020) 2 - p. 439-447 , 2020
Link:
https://doi.org/10.1002/..
?
11
Rare disease patient matchmaking: development and outcomes ..:
LeBlanc, Kimberly
;
Kelley, Emily G
;
Nagy, Anna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108446/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
12
Family genetic result communication in rare and undiagnosed..:
Studwell, Courtney M
;
Kelley, Emily G
;
Undiagnosed Diseases Network
...
qt10q2c8md. , 2021
Link:
https://escholarship.org..
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13
Family Genetic Result Communication in Rare and Undiagnosed..:
Studwell, Courtney M
;
Kelley, Emily G
;
Sinsheimer, Janet S
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207526/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
14
O39: Comprehensive, high-resolution, and non-invasive prena..:
Michael Duyzend
;
Harrison Brand
;
Christopher Whelan
...
http://www.sciencedirect.com/science/article/pii/S2949774423006465. , 2023
Link:
https://doi.org/10.1016/..
?
15
Rare disease patient matchmaking: development and outcomes ..:
Kimberly LeBlanc
;
Emily G. Kelley
;
Anna Nagy
...
https://doi.org/10.1186/s13023-021-01825-1. , 2021
Link:
https://doi.org/10.1186/..
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