Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases.PubCaseFinder: A Case-Report-Based, Phenotype-Driven Differential-Diagnosis System for Rare Diseases

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P2860

Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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http://www.wikidata.org/entity/Q35763184

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

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Hui Yu

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Victor Wei Zhang

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Creative Commons Attribution 3.0 Unported

P2860

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations

Clinical application of exome sequencing in undiagnosed genetic conditions

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

Network medicine: a network-based approach to human disease

High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing

Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project.

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10.1155/2015/745043

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2015

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genetic disease

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Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

about

P2860

P2860

Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases.

description

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type

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P1433

P1476

P2093

P275

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P698

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P932