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Neutrophilic dermatosis in a patient with an IKZF1 variant and a review of monogenic autoinflammatory disorders presenting with neutrophilic dermatoses.
Pediatr Dermatol. 2024 Feb 27. doi: 10.1111/pde.15566. Online ahead of print.
Pediatr Dermatol. 2024.
PMID: 38413050
Shared and distinct mechanisms of UBA1 inactivation across different diseases.
Collins JC, Magaziner SJ, English M, Hassan B, Chen X, Balanda N, Anderson M, Lam A, Fernandez-Pol S, Kwong B, Greenberg PL, Terrier B, Likhite ME, Kosmider O, Wang Y, Samara NL, Walters KJ, Beck DB, Werner A.
Collins JC, et al. Among authors: likhite me.
EMBO J. 2024 May;43(10):1919-1946. doi: 10.1038/s44318-024-00046-z. Epub 2024 Feb 15.
EMBO J. 2024.
PMID: 38360993
Free PMC article.
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Shared and Distinct Mechanisms of UBA1 Inactivation Across Different Diseases.
Collins JC, Magaziner SJ, English M, Hassan B, Chen X, Balanda N, Anderson M, Lam A, Fernandez-Pol S, Kwong B, Greenberg PL, Terrier B, Likhite ME, Kosmider O, Wang Y, Samara NL, Walters KJ, Beck DB, Werner A.
Collins JC, et al. Among authors: likhite me.
bioRxiv [Preprint]. 2023 Oct 10:2023.10.10.561769. doi: 10.1101/2023.10.10.561769.
bioRxiv. 2023.
PMID: 37873213
Free PMC article.
Updated.
Preprint.
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Impact of first-trimester aneuploidy screening in a high-risk population.
Nadel AS, Likhite ML.
Nadel AS, et al. Among authors: likhite ml.
Fetal Diagn Ther. 2009;26(1):29-34. doi: 10.1159/000236356. Epub 2009 Oct 10.
Fetal Diagn Ther. 2009.
PMID: 19816027
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Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis.
Kashork CD, Sutton VR, Fonda Allen JS, Schmidt DE, Likhite ML, Potocki L, O'Brien WE, Shaffer LG.
Kashork CD, et al. Among authors: likhite ml.
Prenat Diagn. 2002 Nov;22(11):1028-32. doi: 10.1002/pd.466.
Prenat Diagn. 2002.
PMID: 12424769
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The Interface Between Countertransference and Projective Identification in a Case Presented to Peer Supervision.
Likhite ML.
Likhite ML.
J Genet Couns. 2000 Oct;9(5):417-24. doi: 10.1023/A:1009406332414.
J Genet Couns. 2000.
PMID: 26141590
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