Genetic Linkage Concept

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A DNA marker closely linked to the factor IX (haemophilia B) gene Journal Articles
A Reanalysis of Protein Polymorphism in Drosophila Melanogaster, D. Simulans, D. Sechellia and D. Mauritiana: Effects of Population Size and Selection Journal Articles
A genetic link between prepregnancy body mass index, postpartum weight retention, and offspring weight in early childhood Journal Articles
A genome-wide linkage and association scan reveals novel loci for autism Journal Articles
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees Journal Articles
A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics Journal Articles
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. Journal Articles
Admixture mapping of male nuptial colour and body shape in a recently formed hybrid population of threespine stickleback Journal Articles
Affected members of melanoma‐prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF Journal Articles
An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis Journal Articles
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. Journal Articles
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage Journal Articles
Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method Journal Articles
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Journal Articles
Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study Journal Articles
Characterization of Three Overlapping Deletions Causing X-Linked Lymphoproliferative Disease Journal Articles
Clinical and Methodological Factors Related to Reliability of the Best-Estimate Diagnostic Procedure Journal Articles
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex. Journal Articles
DNA Marker Studies Show That Machado Joseph Disease is Not an Allele of The Huntingdon Disease Locus Journal Articles
Decomposing the autism phenotype into familial dimensions Journal Articles
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. Journal Articles
Development and Characterization of a Genetic Linkage Map of Cryptococcus neoformans var. neoformans Using Amplified Fragment Length Polymorphisms and Other Markers Journal Articles
Diphtheria-toxin-resistant mutants of CHO cells affected in protein synthesis: A novel phenotype Journal Articles
Dynamic interaction between fetal adversity and a genetic score reflecting dopamine function on developmental outcomes at 36 months Journal Articles
Evidence of linkage in subtypes of alcoholism Journal Articles
Evolutionary origins of two tightly linked mutations in arylsulfatase-A pseudodeficiency Journal Articles
Further localization of X-linked hydrocephalus in the chromosomal region Xq28. Journal Articles
Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Journal Articles
Gene fragmentation in bacterial draft genomes: extent, consequences and mitigation Journal Articles
Generalized epilepsy with febrile seizures plus Journal Articles
Genetic Control of Vulval Development inCaenorhabditis briggsae Journal Articles
Genetic and biochemical characterization of mutants of CHO cells resistant to the protein synthesis inhibitor trichodermin Journal Articles
Genetic control of lymphocyte activation: lack of response to low doses of concanavalin A in lipopolysaccharide-nonresponder mice Journal Articles
Genetic interaction between α4 and β2 subunits of high affinity nicotinic receptor: analysis in schizophrenia Journal Articles
Genetic linkage studies in antithrombin‐deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (str) within the human antithrombin gene Journal Articles
Genetic map of Rhizobium meliloti megaplasmid pRmeSU47b Journal Articles
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Journal Articles
Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I. Journal Articles
Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity Journal Articles
Genome-Wide Association Studies of Hypertension: Have They Been Fruitful? Journal Articles
Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes Journal Articles
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 Journal Articles
Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets Journal Articles
Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders Journal Articles
Genomic Consequences of Background Effects onscallopedMutant Expressivity in the Wing ofDrosophila melanogaster Journal Articles
Genomic organization and linkage via a bidirectional promoter of the AP-3 (adaptor protein-3) mu3A and AK (adenosine kinase) genes: deletion mutants of AK in Chinese hamster cells extend into the AP-3 mu3A gene Journal Articles
HLA-B8 and erythema nodosum. Journal Articles
Heterogeneity and the genetics of autism. Journal Articles
How to Use an Article About Genetic Association Journal Articles
How to Use an Article About Genetic Association Journal Articles
How to Use an Article About Genetic Association Journal Articles
Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl Journal Articles
IQ and the Genetics of Autism Journal Articles
Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders Journal Articles
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome Journal Articles
Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis Journal Articles
Linkage analysis for three coagulation factors clustering on chromosome 13q34: factor VII, factor X and protein Z Journal Articles
Linkage analysis of 26 Canadian breast and breast-ovarian cancer families Journal Articles
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. Journal Articles
Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny Journal Articles
Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37 Journal Articles
Linkage and association analysis in pedigrees from different populations Journal Articles
Localization and linkage of three polymorphic DNA sequences on human chromosome 20 Journal Articles
Localization of X-Linked Dominant Charcot-Marie-Tooth Disease (CMT 2) to Xq13 Journal Articles
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Journal Articles
Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results Journal Articles
Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: Implications for linkage in neurofibromatosis Journal Articles
Mutant Alleles at the Locus elav in Drosophila melanogaster lead to Nervous System Defects. A Developmental-Genetic Analysis Journal Articles
Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women Journal Articles
Population genetics of chronic kidney disease: The evolving story of APOL1 Journal Articles
Random segregation of multiple genetic markers from CHO-CHO hybrids: Evidence for random distribution of functional hemizygosity in the genome Journal Articles
Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere‐FRA(X)‐DXS15‐DXS52‐F8C‐telomere Journal Articles
Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemia. Journal Articles
Regional localization of 18 human X-linked DNA sequences Journal Articles
Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38) Journal Articles
Role of the Cyclin-Dependent Kinase Inhibitor CDKN2A in Familial Melanoma Journal Articles
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees Journal Articles
Sex-Specific Effect of Insulin-Dependent Diabetes 4 on Regulation of Diabetes Pathogenesis in the Nonobese Diabetic Mouse Journal Articles
Stability and peptide binding specificity of Btk SH2 domain: Molecular basis for X‐linked agammaglobulinemia Journal Articles
Studies on temperature-sensitive mutants of Chinese hamster ovary cells affected in DNA synthesis Journal Articles
THE EARLY DETECTION OF DYSTROPHIA MYOTONICA Journal Articles
THE EFFECT OF COMBINING ALLELES INTO ELECTROPHORETIC CLASSES ON DETECTING LINKAGE DISEQUILIBRIUM Journal Articles
THE SAMPLING DISTRIBUTION OF LINKAGE DISEQUILIBRIUM Journal Articles
The DY genes of the cattle MHC: expression and comparative analysis of an unusual class II MHC gene pair Journal Articles
The Diagnosis and Prognosis of Autosomal Dominant Polycystic Kidney Disease Journal Articles
The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications Journal Articles
The HL‐A Type of Rg(a–) Individuals Journal Articles
The association between malathion resistance and acetylcholinesterase in Drosophila melanogaster Journal Articles
The genetics of human personality Journal Articles
The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation. Journal Articles
The search for autism disease genes Journal Articles
The variance of linkage disequilibrium between three loci in a finite population Journal Articles
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia Journal Articles
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes Journal Articles
X-LINKED DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY Journal Articles
[Search for 22q11 deletion and linkage study in familial cases of non-syndromic conotruncal defects]. Journal Articles
ndvF, a novel locus located on megaplasmid pRmeSU47b (pEXO) of Rhizobium meliloti, is required for normal nodule development Journal Articles