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Genetic Counseling
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Viewing resources 1 to 20 of 41 items in this GalterList.
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ABGC - American Board of Genetic Counseling
- * Establishes the standards of competence for clinical practice through accreditation of graduate programs in genetic counseling. Advances the role of genetic counselors in healthcare through the certification and recertification of qualified professionals.
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ALFRED
- ALFRED is a free, web-accessible, curated compilation of allele frequency data on DNA sequence polymorphisms in anthropologically defined human populations. Data in ALFRED are linked to literature, molecular, and ethnographic databases
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AlzGene database
- Tags: alzheimer alzheimer s disease genes genes and disease genetic counseling genetics genome phenotype
- The AlzGene database aims to provide a comprehensive, unbiased and regularly updated collection of genetic association studies performed on Alzheimer’s disease phenotypes.
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Blood Group Antigen Gene Mutation Database (dbRBC)
- NCBI. The Blood Group Antigen Gene Mutation Database (dbRBC) documents variations in genes that directly or indirectly affect blood groups. It thus is a locus-specific mutation database (LSDB) that covers multiple genes.
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BTKbase: X-linked agammaglobulinemia (XLA) | Main page |
- Tags: xla x-linked variation phenotype mutation genotype genes and disease genes btk bruton tyrosine kinase b lymphocytes agammaglobulinemia
- Search for information on defects in the Bruton tyrosine kinase (BTK) gene, which causes agammaglobulinemia (XLA).
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CarpeDB: A Comprehensive Database on the Genetics of Epilepsy
- CarpeDB serves as a novel source for epilepsy researchers by featuring scores of "epilepsy genes" and associated publications in one locus. Furthermore, multiple genes implicated in epilepsy are also implicated in other human disorders.
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CGAP - Cancer Genome Anatomy Project
- The goal of the NCI's Cancer Genome Anatomy Project is to determine the gene expression profiles of normal, precancer, and cancer cells, leading eventually to improved detection, diagnosis, and treatment for the patient. Includes high-quality histology photos of tissue expression.
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Chromosome abnormalities and genetic counseling / R.J. McKinlay Gardner, Grant R. Sutherland
- This is a print book. Click on the link for location information.
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Database of Genomic Variants
- A comprehensive summary of structural variation in the human genome.
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dbGaP Home
- The database of Genotype and Phenotype (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
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Developmental biology
- NCBI online book focusing on the cell and molecular mechanisms of development
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DG-CST Database
- A collection of conserved sequence elements, identified by a systematic genomic sequence comparison between a set of human genes involved in the pathogenesis of genetic disorders and their murine (mouse) counterparts.
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ENCODE Project at UCSC
- Tags: genomics genome studies genome genetics
- Browser and portal for NHGRI's ENCODE project. This is the official repository of sequence-related data for the ENCODE Consortium and supports the coordination of data submission, storage, retrieval, and visualization.
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Fetology : diagnosis and management of the fetal patient
- Electronic book. Includes sections on testing and diagnosis of genetic disorders
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FINDbase Worldwide
- An online repository of information about the frequency of different mutations leading to inherited disorders in various populations around the globe.
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G2D: Candidate Genes to Inherited Diseases
- The Genes2Diseases server presents precomputed candidate genes for more than 600 genetically inherited diseases that have been mapped onto chromosomal regions without assignment of a particular gene.
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GenAtlas
- GENATLAS contains relevant information with respect to gene mapping and genetic diseases. GENATLAS is structured in three databases: Genes database, Phenotypes database, Citations database (linked to the two previous). The information is collected from published literature.
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GeneCards
- GeneCards is an integrated database of human genes that includes automatically-mined genomic, proteomic and transcriptomic information, as well as orthologies, disease relationships, SNPs, gene expression, gene function, and service links for ordering assays and antibodies.
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Genes and disease
- NCBI online resource on genetic basis of disease
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GeneSeeker, CMBI
- CMBI. Gathers and combines data from a series of databases to identify genes underlying human genetic disorders.
