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Kotlarek, Jaclyn R.
12
results:
Search for persons
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Format
Online (12)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (2)
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?
1
Interstitial duplication of 8q22.1‐q23.1‐ A case report and..:
Leary, Steven
;
Porterfield, Harry S.
;
Kotlarek, Jaclyn R.
..
Clinical Case Reports. 7 (2019) 12 - p. 2393-2397 , 2019
Link:
https://doi.org/10.1002/..
?
2
A Familial Case Study Exploring Craniofacial, Velopharyngea..:
Kotlarek, Katelyn J.
;
Kotlarek, Jaclyn R.
;
Reitnauer, Pamela J.
.
Clinical Archives of Communication Disorders. 3 (2018) 3 - p. 236-245 , 2018
Link:
https://doi.org/10.21849..
?
3
Interstitial duplication of 8q22.1‐q23.1‐ A case report and..:
Leary, Steven
;
Porterfield, Harry S
;
Kotlarek, Jaclyn R
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935641/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
4
Interstitial duplication of 8q22.1‐q23.1‐ A case report and..:
Steven Leary
;
Harry S. Porterfield
;
Jaclyn R. Kotlarek
..
https://doi.org/10.1002/ccr3.2507. , 2019
Link:
https://doi.org/10.1002/..
?
5
P145: Paradigm shift in Occam's Razor and the need for geno..:
Tung, Moon Ley
;
Chandra, Bharatendu
;
Nagy, Jaime
...
Genetics in Medicine Open. 2 (2024) - p. 101042 , 2024
Link:
https://doi.org/10.1016/..
?
6
P041: False positive VLCAD deficiency screening: Proposed e..:
McPhillips, Nicole
;
Calhoun, Amy
;
Phillips, Emily
...
Genetics in Medicine Open. 2 (2024) - p. 100918 , 2024
Link:
https://doi.org/10.1016/..
?
7
eP095: A family-based study of hereditary spastic paraplegi..:
Chandra, Bharatendu
;
Romoser, Shelby
;
Kotlarek, Jaclyn
..
Genetics in Medicine. 24 (2022) 3 - p. S62 , 2022
Link:
https://doi.org/10.1016/..
?
8
eP007: Delayed onset hyperammonemic encephalopathy in an ad..:
Chandra, Bharatendu
;
Tung, Moon Ley
;
Surom, Kristen
...
Genetics in Medicine. 24 (2022) 3 - p. S4 , 2022
Link:
https://doi.org/10.1016/..
?
9
TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndr..:
Tung, Moon Ley
;
Chandra, Bharatendu
;
Kotlarek, Jaclyn
...
Genes. 13 (2022) 9 - p. 1649 , 2022
Link:
https://doi.org/10.3390/..
?
10
eP262: De novo heterozygous variant in the RAB11B gene pres..:
Tung, Moon Ley
;
Romoser, Shelby
;
Kotlarek, Jaclyn
...
Genetics in Medicine. 24 (2022) 3 - p. S166 , 2022
Link:
https://doi.org/10.1016/..
?
11
Coexpression of MUC1 mucin peptide core and the thomsen-fri..:
Baldus, Stephan E.
;
Hanisch, Franz-Georg
;
Kotlarek, Georg M.
...
Cancer. 82 (1998) 6 - p. 1019-1027 , 1998
Link:
https://doi.org/10.1002/..
?
12
Mid‐term follow‐up after multiple system organ failure foll..:
Heying, R
;
Seghaye, M‐C
;
Grabitz, RG
...
Acta Paediatrica. 88 (1999) 11 - p. 1238-1243 , 1999
Link:
https://doi.org/10.1111/..
1-12