Whole exome sequencing in patients with congenital cataracts

Acta Ophthalmologica ◽

10.1111/j.1755-3768.2015.0068 ◽

2015 ◽

Vol 93 ◽

pp. n/a-n/a

Author(s):

P. Liskova

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Congenital Cataracts ◽

Download Full-text

A Novel Mutation in CRYGC Identified by Whole Exome Sequencing in a Chinese Families with Autosomal Dominant Congenital Cataracts and Microcornea

SSRN Electronic Journal ◽

10.2139/ssrn.3489292 ◽

2019 ◽

Author(s):

Liying Zhao ◽

Zhenbao Zhou ◽

Jingyi Zhuang ◽

Nan Zhuo ◽

Han Chen ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Autosomal Dominant ◽

Novel Mutation ◽

Congenital Cataracts ◽

Chinese Families ◽

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 ◽

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 ◽

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 ◽

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 ◽

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 ◽

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 ◽

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 ◽

Download Full-text