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The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.
Prenat Diagn. 2024 Mar;44(3):343-351. doi: 10.1002/pd.6527. Epub 2024 Jan 29.
Prenat Diagn. 2024.
PMID: 38285371
Free PMC article.
Prevalence and Clinical Significance of Commonly Diagnosed Genetic Disorders in Preterm Infants.
Everett SS, Bomback M, Sahni R, Wapner RJ, Tolia VN, Clark RH, Lyford A, Hays T.
Everett SS, et al. Among authors: bomback m.
medRxiv [Preprint]. 2023 Sep 8:2023.07.14.23292662. doi: 10.1101/2023.07.14.23292662.
medRxiv. 2023.
PMID: 37503109
Free PMC article.
Preprint.
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The Contribution of Commonly Diagnosed Genetic Disorders to Small for Gestational Age Birth and Subsequent Morbidity and Mortality in Preterm Infants.
Bomback M, Everett S, Lyford A, Sahni R, Kim F, Baptiste C, Motelow JE, Tolia V, Clark R, Hays T.
Bomback M, et al.
medRxiv [Preprint]. 2023 Jul 16:2023.07.14.23292682. doi: 10.1101/2023.07.14.23292682.
medRxiv. 2023.
PMID: 37503041
Free PMC article.
Preprint.
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Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease.
Hays T, Hernan R, Disco M, Griffin EL, Goldshtrom N, Vargas D, Krishnamurthy G, Bomback M, Rehman AU, Wilson AT, Guha S, Phadke S, Okur V, Robinson D, Felice V, Abhyankar A, Jobanputra V, Chung WK.
Hays T, et al. Among authors: bomback m.
Circ Genom Precis Med. 2023 Oct;16(5):415-420. doi: 10.1161/CIRCGEN.122.004050. Epub 2023 Jul 7.
Circ Genom Precis Med. 2023.
PMID: 37417234
Free article.
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