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Dynamic mutation
Adaptive Tuning of Mutation Rates Allows Fast Response to Lethal Stress In
Dynamic Mutations on the Move
General Contribution
Test ID: NGMEM
Genome Mapping Resolves Structural Variation Within Segmental Duplications Associated
Integrative Networks in Intellectual Disabilities
Gene Mutation and DNA Polymorphism Outline of This Chapter
Idiopathic Infertility As a Feature of Genome Instability
By Duplicons Among Patients with Developmental Delay And/Or Congenital Malformations; Detection of Reciprocal and Partial Williams-Beuren Duplications
Genomic Rearrangements of the 7Q11-21 Region
Properties and Rates of Germline Mutations in Humans
Curriculum Vitae
Living Organisms Author Their Read-Write Genomes in Evolution
UNSCEAR 2001 Report to the General Assembly, with Scientific Annex
An Introduction to the Genetics and Epigenetics of Human Disease by Marcus Pembrey
Evolutionary Mechanisms Shaping the Genomic Structure of the Williams-Beuren Syndrome Chromosomal Region at Human 7Q11.23
Gene Identification in Intellectual Disability
Study of Two Bipolar Susceptibility Genes: Slynar and Igf1 1
Top View
The Human Genome; You Gain Some, You Lose Some Kriek, M
Segmental Duplications 73 5 Segmental Duplications
Guest Editorial the Human Gene Mutation Database: Providing a Comprehensive Central Mutation Database for Molecular Diagnostics and Personalised Genomics
Rare Genomic Deletions Underlying Schizophrenia and Related Neurodevelopmental Disorders
Platform Abstracts
Genetic Aspects of Autism Spectrum Disorders: from Bench to Bedside
Chromosomal and Genetic Disorders Malak Alghamdi,MD,Ssc-Ped,ABHS(CH),FCCMG Head of Medical Genetic Division Outlines
Copy Number Variation: New Insights in Genome Diversity
Dynamic Mutations in Human Genes: a Review of Trinucleotide Repeat Diseases
Latest Findings in Intellectual and Developmental Disabilities Research
Genetics Advances and Learning Disability{{ Conditions Are Genetically Heterogeneous (E.G
Evolutionary Analysis of the Highly Dynamic CHEK2 Duplicon in Anthropoids Claudia Münch, Stefan Kirsch, António MG Fernandes and Werner Schempp*
Fragile X Syndrome
What Controls the Length of Noncoding DNA? Josep M Comeron
30198 Molekabya.Pdf
Genomic Rearrangements in Autism Spectrum Disorders: Identification of Novel Candidate Genes
9781907816406.Pdf
Proquest Dissertations
Contribution of Mouse Models for Understanding Diseases Associated
Genetic and Environmental Modifiers of Somatic Trinucleotide Repeat Dynamics
The Dynamic Mutation Investigation and Whole Exome Sequencing in a Cohort of Chinese Autosomal Dominant Cerebellar Ataxia Patients