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Whole Exome Sequencing: A Novel Strategy to Understand Chronic Lung Allograft Dysfunction (CLAD)
The Journal of Heart and Lung Transplantation
◽
10.1016/j.healun.2014.01.377
◽
2014
◽
Vol 33
(4)
◽
pp. S140
◽
Cited By ~ 1
Author(s):
J.L. Todd
◽
T.J. Urban
◽
C.A. Finlen Copeland
◽
F.L. Kelly
◽
D.B. Goldstein
◽
...
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Chronic Lung Allograft Dysfunction
◽
Allograft Dysfunction
◽
Whole Exome
◽
Novel Strategy
Download Full-text
Related Documents
Cited By
References
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Journal of Visualized Experiments
◽
10.3791/53570
◽
2017
◽
Author(s):
Valerio Conti
◽
Aurelie Carabalona
◽
Emilie Pallesi-Pocachard
◽
Richard J. Leventer
◽
Fabienne Schaller
◽
...
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Array Cgh
◽
In Utero
◽
Whole Exome
◽
Brain Malformations
◽
Novel Strategy
Download Full-text
Whole Exome Sequencing (WES) in Familien mit linksventrikulärer Ausfluβtraktobstruktion (LVOTO)
The Thoracic and Cardiovascular Surgeon
◽
10.1055/s-0034-1393993
◽
2014
◽
Vol 62
(S 02)
◽
Author(s):
M. Hitz
◽
S. Al-Turki
◽
A. Schalinski
◽
U. Bauer
◽
T. Pickardt
◽
...
Keyword(s):
Exome Sequencing
◽
Whole Exome Sequencing
◽
Whole Exome
Download Full-text
FV 1031. Whole Exome Sequencing for Children with Dyskinetic Movement Disorder
10.1055/s-0038-1675915
◽
2018
◽
Author(s):
Yasemin Dincer
◽
Michael Zech
◽
Matias Wagner
◽
Nikolai Jung
◽
Volker Mall
◽
...
Keyword(s):
Movement Disorder
◽
Exome Sequencing
◽
Whole Exome Sequencing
◽
Whole Exome
◽
Dyskinetic Movement
Download Full-text
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
Download Full-text
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
◽
Whole Exome
Download Full-text
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
Download Full-text
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
◽
Whole Exome Sequencing
◽
Gene Identification
◽
Congenital Disorders
◽
Type I
◽
Congenital Disorders Of Glycosylation
◽
Whole Exome
Download Full-text
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
Download Full-text
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
◽
Mendelian Disorders
◽
Whole Exome
Download Full-text
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
Download Full-text
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