نتایج جستجو برای: clinical exome sequencing

تعداد نتایج: 1271061  

Journal: :Circulation. Cardiovascular genetics 2017
Sara B Seidelmann Emily Smith Lakshman Subrahmanyan Daniel Dykas Maen D Abou Ziki Bani Azari Fady Hannah-Shmouni Yuexin Jiang Joseph G Akar Mark Marieb Daniel Jacoby Allen E Bale Richard P Lifton Arya Mani

BACKGROUND With the advent of high throughput sequencing, the identification of genetic causes of cardiovascular disease (CVD) has become an integral part of medical diagnosis and management and at the forefront of personalized medicine in this field. The use of whole exome sequencing for clinical diagnosis, risk stratification, and management of inherited CVD has not been previously evaluated....

2016
Alison Hamilton Martine Tétreault David A. Dyment Ruobing Zou Kristin Kernohan Michael T. Geraghty Taila Hartley Kym M. Boycott

The clinical translation of next-generation sequencing has created a paradigm shift in the diagnostic assessment of individuals with suspected rare genetic diseases. Whole-exome sequencing (WES) simultaneously examines the majority of the coding portion of the genome and is rapidly becoming accepted as an efficient alternative to clinical Sanger sequencing for diagnosing genetically heterogeneo...

Journal: :genetics in the 3rd millennium 0
parva namiranian mehrvash shams joseph gleeson hossein najmabadi ariana kariminejad

spastic paraplegia 18 is an autosomal recessive disorder characterized by motor dysfunction, joint contracture and mental retardation. we describe two families as three cases. case 1 is a 35-year-old woman with and spasticity and mild weakness in lower limbs. case 2 and 3 are a sister and brother aged six and two respectively. the older sister suffered from lower limb spasticity, equinovarus an...

2016
Dave Tang Denise Anderson Richard W Francis Genevieve Syn Sarra E Jamieson Timo Lassmann Jenefer M Blackwell

Genetic analyses, including genome-wide association studies and whole exome sequencing (WES), provide powerful tools for the analysis of complex and rare genetic diseases. To date there are no reference data for Aboriginal Australians to underpin the translation of health-based genomic research. Here we provide a catalogue of variants called after sequencing the exomes of 72 Aboriginal individu...

Diana Ramirez-Montaño Estephania Candelo, Harry Pachajoa, Lorena Díaz-Ordoñez Santiago Cruz,

Mutations in the AHDC1 gene are associated with the Xia-Gibbs syndrome (XGS), a sporadic genetic disorder characterised by developmental delay, intellectual disability, hypotonia, obstructive sleep apnoea, dysmorphic facial features, and cerebral malformations with plagiocephaly. Here we report the case of a 13-year-old Colombian female patient with a history of developmental delay, speech dela...

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