Precise Therapy for mCRPC Patients Through Whole Exome Sequencing(PTtWES)

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

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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

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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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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 ◽

Whole Exome Sequencing ◽

Gene Identification ◽

Congenital Disorders ◽

Type I ◽

Congenital Disorders Of Glycosylation ◽

Whole Exome

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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 ◽

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.718131259.793486238 ◽

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

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Faculty Opinions recommendation of Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.718194747.793488319 ◽

2013 ◽

Author(s):

Alon Keinan

Keyword(s):

Type 2 Diabetes ◽

Exome Sequencing ◽

Whole Exome Sequencing ◽

Whole Exome ◽

Coding Variants

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Precise Therapy for mCRPC Patients Through Whole Exome Sequencing(PTtWES)

Whole Exome Sequencing (WES) in Familien mit linksventrikulärer Ausfluβtraktobstruktion (LVOTO)

FV 1031. Whole Exome Sequencing for Children with Dyskinetic Movement Disorder

Genetic characterisation of children with short stature and GH or IGF1 insensitivity by single gene and whole exome sequencing

Faculty Opinions recommendation of Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.

Faculty Opinions recommendation of Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.

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 recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

Faculty Opinions recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

Faculty Opinions recommendation of Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

Faculty Opinions recommendation of Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.

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