Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing
Publication
, Journal Article
Rentas, S; Rathi, KS; Kaur, M; Raman, P; Krantz, ID; Sarmady, M; Tayoun, AA
Published in: Genetics in Medicine
May 2020
Duke Scholars
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Published In
Genetics in Medicine
DOI
ISSN
1098-3600
Publication Date
May 2020
Volume
22
Issue
5
Start / End Page
927 / 936
Publisher
Elsevier BV
Related Subject Headings
- Genetics & Heredity
- 1103 Clinical Sciences
- 0604 Genetics
Citation
APA
Chicago
ICMJE
MLA
NLM
Rentas, S., Rathi, K. S., Kaur, M., Raman, P., Krantz, I. D., Sarmady, M., & Tayoun, A. A. (2020). Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing. Genetics in Medicine, 22(5), 927–936. https://doi.org/10.1038/s41436-019-0741-5
Rentas, Stefan, Komal S. Rathi, Maninder Kaur, Pichai Raman, Ian D. Krantz, Mahdi Sarmady, and Ahmad Abou Tayoun. “Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing.” Genetics in Medicine 22, no. 5 (May 2020): 927–36. https://doi.org/10.1038/s41436-019-0741-5.
Rentas S, Rathi KS, Kaur M, Raman P, Krantz ID, Sarmady M, et al. Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing. Genetics in Medicine. 2020 May;22(5):927–36.
Rentas, Stefan, et al. “Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing.” Genetics in Medicine, vol. 22, no. 5, Elsevier BV, May 2020, pp. 927–36. Crossref, doi:10.1038/s41436-019-0741-5.
Rentas S, Rathi KS, Kaur M, Raman P, Krantz ID, Sarmady M, Tayoun AA. Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing. Genetics in Medicine. Elsevier BV; 2020 May;22(5):927–936.
Published In
Genetics in Medicine
DOI
ISSN
1098-3600
Publication Date
May 2020
Volume
22
Issue
5
Start / End Page
927 / 936
Publisher
Elsevier BV
Related Subject Headings
- Genetics & Heredity
- 1103 Clinical Sciences
- 0604 Genetics