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Mowrey, Kate
31
results:
Search for persons
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Format
Online (31)
Mediatypes
Articles (Online) (16)
OpenAccess-fulltext (15)
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?
1
Genetics in the NICU: Nurses' Perceived Knowledge and Desir..:
Shields, Kathleen
;
Czerwinski, Jennifer
;
Dauwe, Tracie
...
The Journal of Continuing Education in Nursing. 54 (2023) 1 - p. 16-24 , 2023
Link:
https://doi.org/10.3928/..
?
2
42428 Rapid Response to Sirolimus in Patients with PIK3CA-R..:
Nye, Jessica
;
Green, Jackson
;
Greives, Matthew
...
Journal of the American Academy of Dermatology. 89 (2023) 3 - p. AB81 , 2023
Link:
https://doi.org/10.1016/..
?
3
Malignant Melanoma within a Giant Congenital Melanocytic Ne..:
Green, Jackson
;
Nye, Jessica
;
Turner, Kelly
...
SKIN The Journal of Cutaneous Medicine. 7 (2023) 1 - p. 608-611 , 2023
Link:
https://doi.org/10.25251..
?
4
eP194: Three generations of females with a heterozygous lik..:
Mowrey, Kate
;
Northrup, Hope
Genetics in Medicine. 24 (2022) 3 - p. S120 , 2022
Link:
https://doi.org/10.1016/..
?
5
Case Report: Novel pathogenic variant in NFIX in two sister..:
Langley, Elizabeth
;
Farach, Laura S.
;
Mowrey, Kate
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
6
NEXMIF pathogenic variants in individuals of Korean, Vietna..:
Langley, Elizabeth
;
Farach, Laura S.
;
Koenig, Mary K.
...
American Journal of Medical Genetics Part A. 188 (2022) 6 - p. 1688-1692 , 2022
Link:
https://doi.org/10.1002/..
?
7
eP163: Germline mosaicism in two sisters with Malan syndrom:
Langley, Elizabeth
;
Mowrey, Kate
;
Farach, Laura
Genetics in Medicine. 24 (2022) 3 - p. S99-S100 , 2022
Link:
https://doi.org/10.1016/..
?
8
Expanding Our Knowledge of Menstrual Irregularities Reporte..:
Mowrey, Kate
;
Northrup, Hope
;
Hashmi, Syed Shahrukh
.
Frontiers in Reproductive Health. 4 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
9
Identification of a novel microdeletion causative of Nance‐..:
Lopez Martinolich, Mariana
;
Northrup, Hope
;
Mancias, Pedro
...
Molecular Genetics & Genomic Medicine. 10 (2022) 3 - p. , 2022
Link:
https://doi.org/10.1002/..
?
10
eP246: Novel EFTUD2 variant adds to understanding of phenot..:
Shields, Kathleen
;
Mowrey, Kate
;
Hillman, Paul
Genetics in Medicine. 24 (2022) 3 - p. S156-S157 , 2022
Link:
https://doi.org/10.1016/..
?
11
A de novo case of autosomal dominant mitochondrial Membrane..:
Mowrey, Kate
;
Fraser, Stuart
;
Koenig, Mary Kay
..
Molecular Genetics and Metabolism. 132 (2021) - p. S119-S120 , 2021
Link:
https://doi.org/10.1016/..
?
12
A De Novo case of autosomal dominant mitochondrial membrane..:
Fraser, Stuart
;
Koenig, Mary
;
Farach, Laura
..
Molecular Genetics & Genomic Medicine. 9 (2021) 7 - p. , 2021
Link:
https://doi.org/10.1002/..
?
13
Frequency, Progression, and Current Management: Report of 1..:
Mowrey, Kate
;
Northrup, Hope
;
Rougeau, Peyton
...
Frontiers in Neurology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
14
Two new reported cases of 16q22.3q23.3 duplication syndrome..:
Gunther, Kathryn
;
Mowrey, Kate
;
Farach, Laura Schoch
Clinical Case Reports. 9 (2021) 3 - p. 1629-1633 , 2021
Link:
https://doi.org/10.1002/..
?
15
Two different genetic etiologies for tuberous sclerosis com..:
Mowrey, Kate
;
Koenig, Mary Kay
;
Szabo, Charles A.
...
Molecular Genetics & Genomic Medicine. 8 (2020) 7 - p. , 2020
Link:
https://doi.org/10.1002/..
1-15