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497: ASSOCIATION OF WHOLE EXOME SEQUENCING WITH SEVERITY OF ILLNESS IN THE PEDIATRIC ICU
Critical Care Medicine
◽
10.1097/01.ccm.0000808312.52796.5d
◽
2021
◽
Vol 50
(1)
◽
pp. 240-240
Author(s):
Zachary Daniels
◽
Kevin Morrison
◽
L. Nelson Sanchez-Pinto
◽
Divakar Mithal
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Severity Of Illness
◽
Whole Exome
◽
Pediatric Icu
Download Full-text
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Whole Exome Sequencing (WES) in Familien mit linksventrikulärer Ausfluβtraktobstruktion (LVOTO)
The Thoracic and Cardiovascular Surgeon
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◽
2014
◽
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◽
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◽
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◽
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FV 1031. Whole Exome Sequencing for Children with Dyskinetic Movement Disorder
10.1055/s-0038-1675915
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2018
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Author(s):
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◽
Michael Zech
◽
Matias Wagner
◽
Nikolai Jung
◽
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◽
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◽
Exome Sequencing
◽
Whole Exome Sequencing
◽
Whole Exome
◽
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Genetic characterisation of children with short stature and GH or IGF1 insensitivity by single gene and whole exome sequencing
Endocrine Abstracts
◽
10.1530/endoabs.39.oc5.2
◽
2015
◽
Author(s):
Lucy Shapiro
◽
Martin Savage
◽
Lou Metherell
◽
Helen Storr
Keyword(s):
Short Stature
◽
Exome Sequencing
◽
Whole Exome Sequencing
◽
Single Gene
◽
Genetic Characterisation
◽
Whole Exome
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Precise Therapy for mCRPC Patients Through Whole Exome Sequencing(PTtWES)
Case Medical Research
◽
10.31525/ct1-nct04126915
◽
2019
◽
Author(s):
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
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Whole Exome
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Faculty Opinions recommendation of Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.5376956.9620054
◽
2011
◽
Author(s):
David Glahn
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Whole Exome
◽
Brain Malformations
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Faculty Opinions recommendation of Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.717956777.793461365
◽
2012
◽
Author(s):
Jane Hewitt
Keyword(s):
Exome Sequencing
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Whole Exome Sequencing
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◽
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◽
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◽
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Faculty Opinions recommendation of Whole-exome sequencing reveals a heterozygous LRP5 mutation in a 6-year-old boy with vertebral compression fractures and low trabecular bone density.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718048076.793481338
◽
2013
◽
Author(s):
Wim van Hul
Keyword(s):
Bone Density
◽
Trabecular Bone
◽
Exome Sequencing
◽
Whole Exome Sequencing
◽
Vertebral Compression Fractures
◽
Trabecular Bone Density
◽
Compression Fractures
◽
Whole Exome
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Faculty Opinions recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718131259.793487604
◽
2013
◽
Author(s):
Marc S Williams
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
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◽
Whole Exome
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Faculty Opinions recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718131259.793486238
◽
2013
◽
Author(s):
Gail Herman
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Mendelian Disorders
◽
Whole Exome
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Faculty Opinions recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718131259.793486015
◽
2014
◽
Author(s):
François Cambien
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Mendelian Disorders
◽
Whole Exome
Download Full-text
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