<--- Back to Details
First PageDocument Content
Molecular biology / Genomics / Medical genetics / Channelopathy / DNA / Exome sequencing / Full genome sequencing / Compound heterozygosity / Genetic testing / Biology / Medicine / Genetics
Date: 2013-09-10 11:51:06
Molecular biology
Genomics
Medical genetics
Channelopathy
DNA
Exome sequencing
Full genome sequencing
Compound heterozygosity
Genetic testing
Biology
Medicine
Genetics

BLU[removed]#03revisedfig1.2

Add to Reading List

Source URL: www.bcbs.com

Download Document from Source Website

File Size: 210,52 KB

Share Document on Facebook

Similar Documents

Haploinsufficiency / Compound heterozygosity / Genetic variation / Penetrance / Population genetics / Genomes Project / Genome-wide association study / Single-nucleotide polymorphism / Human genome / Biology / Genetics / Philosophy of biology

Clan Genomics and the Complex Architecture of Human Disease

DocID: 1fNzo - View Document

Exome sequencing / Human genome / Mutation / Compound heterozygosity / Full genome sequencing / Mosaic / Genetic architecture / Timothy syndrome / Epigenetics / Biology / Genetics / Philosophy of biology

Manuscript_Book_chapter_Version5_09272013

DocID: 1al8z - View Document

Mutation / Brevican / Compound heterozygosity / SNP genotyping / Single-nucleotide polymorphism / Restriction fragment length polymorphism / Genotype / Genome-wide association study / Genotyping / Biology / Genetics / Philosophy of biology

Parallel Mapping and Simultaneous Sequencing Reveals Deletions in BCAN and FAM83H Associated with Discrete Inherited Disorders in a Domestic Dog Breed Oliver P. Forman1*, Jacques Penderis2., Claudia Hartley1., Louisa J.

DocID: 18OdV - View Document

Health / Thalassemia / Beta-thalassemia / Hemoglobinopathy / Hemoglobin / Compound heterozygosity / Alpha-thalassemia / Sickle-cell disease / Fetal hemoglobin / Hemoglobins / Medicine / Biology

60 International Journal of Modern Anthropology Int. J. Mod. Anthrop: 60-78 Available online at: www.ata.org.tn ;

DocID: 18jWZ - View Document

Preimplantation genetic diagnosis / Polymerase chain reaction / Point mutation / Thalassemia / Compound heterozygosity / Sickle-cell disease / Single-strand conformation polymorphism / Temperature gradient gel electrophoresis / Biology / Genetics / Molecular biology

Molecular Human Reproduction vol.3 no.8 pp. 693–698, 1997 Single cell detection of β-thalassaemia mutations using silver stained SSCP analysis: an application for preimplantation diagnosis Nisreen El-Hashemite, Daga

DocID: 18cCl - View Document