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Bowling, Kevin M.
~ 700
results:
Search for persons
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Format
Online
Mediatypes
E-Books
Articles (Online)
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OpenAccess-fulltext
Sorted by: Relevance
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?
1
Parents' Perspectives on the Utility of Genomic Sequencing ..:
Lemke, Amy A.
;
Thompson, Michelle L.
;
Gimpel, Emily C.
...
Journal of Personalized Medicine. 13 (2023) 7 - p. 1026 , 2023
Link:
https://doi.org/10.3390/..
?
2
Poison exon annotations improve the yield of clinically rel..:
Felker, Stephanie A.
;
Lawlor, James M.J.
;
Hiatt, Susan M.
...
Genetics in Medicine. 25 (2023) 8 - p. 100884 , 2023
Link:
https://doi.org/10.1016/..
?
3
338 The Alabama Genomic Health Initiative: Integrating Geno..:
Limdi, Nita A
;
Absher, Devin
;
Asif, Irf
...
Journal of Clinical and Translational Science. 7 (2023) s1 - p. 100-101 , 2023
Link:
https://doi.org/10.1017/..
?
4
Genome sequencing as a first-line diagnostic test for hospi..:
Bowling, Kevin M.
;
Thompson, Michelle L.
;
Finnila, Candice R.
...
Genetics in Medicine. 24 (2022) 4 - p. 851-861 , 2022
Link:
https://doi.org/10.1016/..
?
5
Return of non-ACMG recommended incidental genetic findings ..:
Bowling, Kevin M.
;
Thompson, Michelle L.
;
Kelly, Melissa A.
...
Genome Medicine. 14 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
6
Identifying rare, medically relevant variation via populati..:
Bowling, Kevin M.
;
Thompson, Michelle L.
;
Gray, David E.
...
Genetics in Medicine. 23 (2021) 2 - p. 280-288 , 2021
Link:
https://doi.org/10.1038/..
?
7
A state-based approach to genomics for rare disease and pop..:
East, Kelly M.
;
Kelley, Whitley V.
;
Cannon, Ashley
...
Genetics in Medicine. 23 (2021) 4 - p. 777-781 , 2021
Link:
https://doi.org/10.1038/..
?
8
Long-read genome sequencing for the molecular diagnosis of ..:
Hiatt, Susan M.
;
Lawlor, James M.J.
;
Handley, Lori H.
...
Human Genetics and Genomics Advances. 2 (2021) 2 - p. 100023 , 2021
Link:
https://doi.org/10.1016/..
?
9
Phenotypic expansion of the BPTF‐related neurodevelopmental..:
Glinton, Kevin E.
;
Hurst, Anna C. E.
;
Bowling, Kevin M.
...
American Journal of Medical Genetics Part A. 185 (2021) 5 - p. 1366-1378 , 2021
Link:
https://doi.org/10.1002/..
?
10
How secondary findings are made:
, In:
Secondary Findings in Genomic Research
,
Bowling, Kevin M.
;
Thompson, Michelle L.
;
Cooper, Gregory M.
- p. 59-75 , 2020
Link:
https://doi.org/10.1016/..
?
11
Contributors:
, In:
Secondary Findings in Genomic Research
,
Berg, Jonathan S.
;
Bertier, Gabrielle
;
Bowling, Kevin M.
... - p. xi-xiii , 2020
Link:
https://doi.org/10.1016/..
?
12
Variants in TCF20 in neurodevelopmental disability: descrip..:
Torti, Erin
;
Keren, Boris
;
Palmer, Elizabeth E.
...
Genetics in Medicine. 21 (2019) 9 - p. 2036-2042 , 2019
Link:
https://doi.org/10.1038/..
?
13
Correction: Secondary findings from clinical genomic sequen..:
Hart, M. Ragan
;
Biesecker, Barbara B.
;
Blout, Carrie L.
...
Genetics in Medicine. 21 (2019) 5 - p. 1261-1262 , 2019
Link:
https://doi.org/10.1038/..
?
14
Secondary findings from clinical genomic sequencing: preval..:
Hart, M. Ragan
;
Biesecker, Barbara B.
;
Blout, Carrie L.
...
Genetics in Medicine. 21 (2019) 5 - p. 1100-1110 , 2019
Link:
https://doi.org/10.1038/..
?
15
De novo mutations in MED13, a component of the Mediator com..:
The DDD study
;
Snijders Blok, Lot
;
Hiatt, Susan M.
...
Human Genetics. 137 (2018) 5 - p. 375-388 , 2018
Link:
https://doi.org/10.1007/..
1-15