E-LIB Suche - Ergebnisse für: Scott, Abbey

1

P894: Limitations in access to genetic counseling training ..:

Meyer, Sophia ; Scott, Abbey ; Gabriel, Camila.
Genetics in Medicine Open. 2 (2024) - p. 101808 , 2024

Link: https://doi.org/10.1016/..

2

P214: SeqFirst DDi: Early whole genome sequencing improves ..:

Dipple, Katrina ; Doherty, Daniel ; Anderson, Kailyn...
Genetics in Medicine Open. 2 (2024) - p. 101111 , 2024

Link: https://doi.org/10.1016/..

3

P193: Inpatient genetics consults for nondysmorphic childre..:

Keefe, Alexandra ; Scott, Abbey ; Kruidenier, Lukas...
Genetics in Medicine Open. 2 (2024) - p. 101090 , 2024

Link: https://doi.org/10.1016/..

4

P487: Increasing access to precise genetic diagnoses for in..:

Scott, Abbey ; Kruidenier, Lukas ; Sikes, Megan...
Genetics in Medicine Open. 2 (2024) - p. 101386 , 2024

Link: https://doi.org/10.1016/..

5

P194: SeqFirst mitigates race-based disparities in access t..:

Wenger, Tara ; Keefe, Alexandra ; Kruidenier, Lukas...
Genetics in Medicine Open. 2 (2024) - p. 101091 , 2024

Link: https://doi.org/10.1016/..

6

P208: SeqFirst: Impact of a precise genetic diagnosis on en..:

Keefe, Alexandra ; Wenger, Tara ; Yu, Joon-Ho...
Genetics in Medicine Open. 1 (2023) 1 - p. 100236 , 2023

Link: https://doi.org/10.1016/..

7

P414: SeqFirst: Parental perspectives on receiving results ..:

Wenger, Tara ; Keefe, Alexandra ; Sikes, Megan...
Genetics in Medicine Open. 1 (2023) 1 - p. 100450 , 2023

Link: https://doi.org/10.1016/..

8

Subdural hemorrhage, macrocephaly, rash, and developmental ..:

Koti, Ajay S. ; Lanis, Aviya ; Finlayson, Samuel...
American Journal of Medical Genetics Part A. 191 (2023) 12 - p. 2825-2830 , 2023

Link: https://doi.org/10.1002/..

9

A recurrent, de novo pathogenic variant in ARPC4 disrupts a..:

Laboy Cintron, Dianne ; Muir, Alison M. ; Scott, Abbey...
Human Genetics and Genomics Advances. 3 (2022) 1 - p. 100072 , 2022

Link: https://doi.org/10.1016/..

10

eP509: Implementation and impact of dedicated inpatient gen..:

Scott, Abbey ; Sikes, Megan ; Wenger, Tara
Genetics in Medicine. 24 (2022) 3 - p. S324-S325 , 2022

Link: https://doi.org/10.1016/..

11

eP281: SeqFirst-neo: Improving access equity for a precise ..:

Wenger, Tara ; Scott, Abbey ; Sikes, Megan...
Genetics in Medicine. 24 (2022) 3 - p. S178 , 2022

Link: https://doi.org/10.1016/..

12

De novo and biallelic DEAF1 variants cause a phenotypic spe..:

Nabais Sá, Maria J. ; Jensik, Philip J. ; McGee, Stacey R....
Genetics in Medicine. 21 (2019) 9 - p. 2059-2069 , 2019

Link: https://doi.org/10.1038/..

13

Long-term effects of stand density management and genotype ..:

Blazier, Michael A. ; Hennessey, Thomas ; Schimleck, Laurence...
Forest Ecology and Management. 491 (2021) - p. 119176 , 2021

Link: https://doi.org/10.1016/..

14

De novo and biallelic DEAF1 variants cause a phenotypic spe..:

Nabais Sá, Maria J ; Jensik, Philip J ; McGee, Stacey R...
https://discovery.dundee.ac.uk/en/publications/74492ddf-8fe6-481c-8017-0598263aa0aa. , 2019

Link: https://discovery.dundee..

15

P414: SeqFirst: Parental perspectives on receiving results ..:

Tara Wenger ; Alexandra Keefe ; Megan Sikes...
http://www.sciencedirect.com/science/article/pii/S2949774423004508. , 2023

Link: https://doi.org/10.1016/..