1,680 Artículos relativos a Escala de Lod

• Epistasis effect: an alternative to the hypothesis of linkage disequilibrium in HLA associated diseases.
  Publicado en Ann Hum Genet
• Utility of genetic markers in the study of human resemblance.
  Publicado en Acta Genet Med Gemellol (Roma)
• A collaborative study of genetic linkage of bipolar manic-depressive illness and red/green colorblindness. A project of the biological psychiatry collaborative program of the world health organization.
  Publicado en Acta Psychiatr Scand
• Hereditary spherocytosis linkage.
  Publicado en Br J Haematol
• Application of the lod score method to detection of linkage between HLA and juvenile insulin-dependent diabetes.
  Publicado en Clin Genet
• Ataxia-telangiectasia and xeroderma pigmentosum: no evidence of linkage to HLA.
  Publicado en Tissue Antigens
• Genetic linkage studies in Huntington's chorea.
  Publicado en Ann Hum Genet
• Juvenile insulin-dependent diabetes: a possible susceptibility gene in interaction with HLA.
  Publicado en Ann Hum Genet
• Linkage relationship of the loci for Anderson--Fabry disease and the Xg blood groups.
  Publicado en Ann Hum Genet
• The MNSs blood groups of families with chromosome 4 rearrangements.
  Publicado en Ann Hum Genet
• Family studies on nucleoside phosphorylase and the short arm of chromosome 14.
  Publicado en Ann Hum Genet
• Close genetic linkage between diabetes mellitus and kidd blood group.
  Publicado en Lancet
• Genetic linkage analysis of dermo-distortive urticaria.
  Publicado en Am J Med Genet
• Linkage investigations in two families with hereditary ataxia.
  Publicado en J Neurol Neurosurg Psychiatry
• X-linkage in bipolar affective illness. Perspectives on genetic heterogeneity, pedigree analysis and the X-chromosome map.
  Publicado en J Affect Disord
• A new genetic model proposing that the Se gene is a structural gene closely linked to the H gene.
  Publicado en Am J Hum Genet
• Some epistatic two-locus models of disease. II. The confounding of linkage and association.
  Publicado en Am J Hum Genet
• Monoclonal rat anti-MHC alloantibodies detect HLA-linked polymorphisms in humans.
  Publicado en Immunogenetics
• Population, formal genetics, and linkage relations of the phosphoglycolate phosphatase (PGP)--E.C.3.1.3.18.
  Publicado en Hum Genet
• Genetics of Type I diabetes mellitus: a single, recessive predisposition gene mapping between HLA-B and GLO. With an appendix on the estimation of selection bias.
  Publicado en Am J Hum Genet
• No evidence for linkage between diabetes and the Kidd marker.
  Publicado en Diabetes
• HLA antigens in Yugoslav patients with palmoplantar keratoderma, type Unna-Thost: a family study.
  Publicado en Acta Derm Venereol
• A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.
  Publicado en Am J Med Genet
• No evidence for linkage between HLA and maturity onset type of diabetes in young people.
  Publicado en Diabetologia
• X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data.
  Publicado en Ann Hum Genet
• Mapping studies on human mitochondrial glutamate oxaloacetate transaminase.
  Publicado en Ann Hum Genet
• Absence of close linkage between acute intermittent porphyria and the ABO, Rh, P, acid phosphatase, Pr, orosmucoid and pepsinogen loci.
  Publicado en Hum Hered
• Genetic aspects of nonchromaffin paraganglioma.
  Publicado en Hum Genet
• Heterogeneity of insulin-dependent diabetes-new evidence.
  Publicado en Clin Genet
• Evidence for linkage of type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
  Publicado en Ann Hum Genet
• Linkage between dentinogenesis imperfecta and Gc.
  Publicado en Ann Hum Genet
• Confirmation of linkage between antithrombin III and Duffy blood group and assignment of AT3 to 1q22 lead to q25.
  Publicado en Ann Hum Genet
• Die familiär gehäufte Rekurrensparese ein genetisch fixiertes Syndrom -- erneut Hinweise für eine Kopplung des Defektgens mit dem HLA-System.
  Publicado en Laryngol Rhinol Otol (Stuttg)
• Linkage analysis with the trismus-pseudocamptodactyly syndrome.
  Publicado en Am J Med Genet
• The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man.
  Publicado en Hum Genet
• Analysis of linkage relationships in maturity-onset diabetes of young people and independent segregation of C6 and HLA.
  Publicado en Hum Genet
• Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.
  Publicado en Am J Hum Genet
• Tangier disease: heterozygote detection and linkage analysis.
  Publicado en Hum Genet
• Genetic heterogeneity for fingertip arches.
  Publicado en Am J Hum Genet
• Possible assignment of a dominant retinitis pigmentosa gene to chromosome 1.
  Publicado en Ophthalmic Res
• Autosomal dominant ophthalmologic disorders and linkage.
  Publicado en J Pediatr Ophthalmol Strabismus
• Bias of the estimated recombination fraction and lod score due to an association between a disease gene and a marker gene.
  Publicado en Ann Hum Genet
• Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.
  Publicado en Hum Genet
• Evidence for linkage between the loci for transferrin and ceruloplasmin in man.
  Publicado en Ann Hum Genet
• Genetic polymorphism of the LW blood group system.
  Publicado en Ann Hum Genet
• X-linked inheritance of Alport syndrome: family P revisited.
  Publicado en Am J Hum Genet
• Linkage analysis in dominant optic atrophy.
  Publicado en Am J Hum Genet
• The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.
  Publicado en Am J Hum Genet
• A DNA polymorphism in close physical linkage with the proopiomelanocortin gene.
  Publicado en Am J Hum Genet
• Linkage analysis of neurofibromatosis (von Recklinghausen disease).
  Publicado en J Med Genet
• Genetic linkage studies with cleft lip and palate: report of two family studies.
  Publicado en J Craniofac Genet Dev Biol
• A search for linkage in families with fragile sites.
  Publicado en Hum Genet
• Evidence that the Menkes locus maps on proximal Xp.
  Publicado en Hum Genet
• Genetics of human S-adenosylhomocysteine hydrolase. A new polymorphism in man.
  Publicado en Hum Genet
• On the genetic length of the short arm of the human X chromosome.
  Publicado en Hum Genet
• Genetic linkage between the loci for myotonic dystrophy and peptidase D.
  Publicado en Ann Hum Genet
• Association and linkage studies of genetic marker loci in major psychiatric disorders.
  Publicado en Psychiatr Dev
• Genetic mapping: X chromosome.
  Publicado en Hum Genet
• Genetic analysis of multiply-affected families of insulin-dependent diabetes mellitus (IDDM) probands.
  Publicado en Hum Hered
• Vyznam genetickych markeru pro psychiatricky vyzkum.
  Publicado en Cesk Psychiatr
• Absence of close linkage between Hereditary spherocytosis (SPH) and 24 genetic marker systems including HLA and GM.
  Publicado en Ann Hum Genet
• Genetic linkage data for the Dombrock blood group locus relative to chromosome 1 and chromosome 4 loci.
  Publicado en Ann Hum Genet
• Segregation and linkage analyses in families of patients with bipolar, unipolar, and schizoaffective mood disorders.
  Publicado en Am J Hum Genet
• Heterozygous expression of insulin-dependent diabetes mellitus (IDDM) determinants in the HLA system.
  Publicado en Am J Hum Genet
• Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locus.
  Publicado en Am J Hum Genet
• The inheritance of immunoglobulin E: genetic linkage analysis.
  Publicado en Am J Med Genet
• Study of a form of pulverulent cataract in a large kindred.
  Publicado en J Med Genet
• A linkage study between HLA and cutaneous malignant melanoma or precursor lesions or both.
  Publicado en J Med Genet
• Estimating the recombination frequency for the MN and the Ss loci.
  Publicado en Hum Hered
• X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked.
  Publicado en Hum Genet
• No evidence for linkage between an insulin-dependent diabetes mellitus-susceptibility locus and immunoglobulin loci KM or GM.
  Publicado en Genet Epidemiol
• Possible linkage of a breast cancer-susceptibility locus to the ABO locus: sensitivity of LOD scores to a single new recombinant observation.
  Publicado en Genet Epidemiol
• Interpretation of LOD scores with a set of marker loci.
  Publicado en Genet Epidemiol
• Linkage analysis in lattice corneal dystrophy.
  Publicado en Am J Med Genet
• The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia.
  Publicado en Atherosclerosis
• On the lod score method in linkage analysis.
  Publicado en Ann Hum Genet
• Family data on sixteen chromosome 1 loci.
  Publicado en Ann Hum Genet
• HLA-associated diseases: a new method for performing linkage analysis with other markers than HLA.
  Publicado en Am J Hum Genet
• Linkage between X-chromosome markers and manic-depressive illness. Two Sardinian pedigrees.
  Publicado en Acta Psychiatr Scand
• C3 polymorphism, HLA and chronic renal failure in Spaniards.
  Publicado en Hum Genet
• The gene for coagulation factor XIII a subunit (F13A) is distal to HLA on chromosome 6.
  Publicado en Hum Genet
• Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage.
  Publicado en Am J Hum Genet
• Linkage of plasma alpha-L-fucosidase (FUCA2) and the plasminogen (PLG) system.
  Publicado en Clin Genet
• A revised map of chromosome 1.
  Publicado en Ann Hum Genet
• Linkage of the LW blood group locus with the complement C3 and Lutheran blood group loci.
  Publicado en Ann Hum Genet
• The rare Lutheran blood group phenotype Lu(a-b-): a genetic study.
  Publicado en Ann Hum Genet
• Genetic linkage studies of transferrin, pseudocholinesterase, and chromosome 1 loci.
  Publicado en Hum Hered
• Estimating the recombination frequency for the PTC-Kell linkage.
  Publicado en Hum Genet
• The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19.
  Publicado en Hum Genet
• Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families.
  Publicado en Hum Genet
• Coagulation factor XIII: a useful polymorphic genetic marker.
  Publicado en Hum Genet
• Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.
  Publicado en Hum Genet
• Familial hypocalciuric hypercalcaemia: association with neonatal primary hyperparathyroidism, and possible linkage with HLA haplotype.
  Publicado en Clin Endocrinol (Oxf)
• Linkage studies in Menkes' disease. The Xg blood group system and C-banding of the X chromosome.
  Publicado en Ann Hum Genet
• Sampling considerations in the design and analysis of family studies.
  Publicado en Prog Clin Biol Res
• The impact of RFLPs on human gene mapping.
  Publicado en Prog Clin Biol Res
• Linkage and association.
  Publicado en Prog Clin Biol Res
• Easy calculations of lod scores and genetic risks on small computers.
  Publicado en Am J Hum Genet
• c-Ha-ras-1 oncogene lies between beta-globin and insulin loci on human chromosome 11p.
  Publicado en Am J Hum Genet
• Linkage between late onset, dominant spinocerebellar ataxia and HLA.
  Publicado en Hum Genet