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Journal Article
Genomics, ISSN 0888-7543, 1994, Volume 24, Issue 2, pp. 225 - 233
Automation of the typing of genetic markers offers advantages of speed, accuracy, and cost in the mapping of genetic traits and the construction of... 
ORIGIN | POLYMORPHISMS | SEQUENCES | TANDEM REPEATS | CLONING | DNA | GENETICS & HEREDITY | PCR-ANALYZED MICROSATELLITES | CHROMOSOME-20 | MAP | GENOME | Automation | Alleles | Polymerase Chain Reaction | DNA, Satellite - genetics | Genotype | Genetic Markers | Genetic Techniques | Fluorescent Dyes | Genetic Linkage | Index Medicus
Journal Article
IMMUNOGENETICS, ISSN 0093-7711, 08/2003, Volume 55, Issue 5, pp. 344 - 350
The rat major histocompatibility complex loci RT1-B and RT1-D are equivalent to the human leucocyte antigens HLA-DQ and HLA-DR respectively. Here we describe... 
rat | class II MHC sequence | ANTIGENS | MAJOR HISTOCOMPATIBILITY COMPLEX | CDNA | POLYMORPHISM | IMMUNOLOGY | DIABETIC BB-RAT | RESPONSES | GENE | GENETICS & HEREDITY | RT1(u) haplotype | CHROMOSOME-20 | 1ST DOMAIN | cloning | LEWIS RAT
Journal Article
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, ISSN 0021-972X, 08/1994, Volume 79, Issue 2, pp. 421 - 427
The molecular basis of autosomal dominant neurohypophyseal diabetes insipidus, a hereditary deficiency of vasopressin, was determined by nucleotide sequence... 
SIGNAL | VASOPRESSIN V2-RECEPTOR GENE | ARGININE-VASOPRESSIN | PRECURSOR | HORMONE | DEFECT | ENDOCRINOLOGY & METABOLISM | RECEPTOR GENE | CHROMOSOME-20 | BRATTLEBORO RATS | PEPTIDE
Journal Article
Journal Article
HUMAN GENETICS, ISSN 0340-6717, 06/1995, Volume 95, Issue 6, pp. 687 - 690
Alagille syndrome (AGS) or arteriohepatic dysplasia is a rare but well-defined clinical entity that is usually inherited as an autosomal dominant trait. A... 
PAIRED BOX | 20P | GENES | GENETICS & HEREDITY | SYNDROME ARTERIOHEPATIC DYSPLASIA | CHROMOSOME-20 | PAX-1 | DELETION | MEMBER
Journal Article
Annals of Neurology, ISSN 0364-5134, 1991, Volume 29, Issue 5, pp. 469 - 473
The gene for autosomal dominant "benign" familial neonatal convulsions, a transient, primary epilepsy of infancy, has recently been assigned to chromosome 20q.... 
MARKERS | CHROMOSOME-20 | LINKAGE | NEUROSCIENCES | CLINICAL NEUROLOGY | MARIE-TOOTH NEUROPATHY | Genetic Testing | Humans | Genotype | Phenotype | DNA - analysis | Pedigree | Recombination, Genetic | Epilepsy - genetics | Family | Female | Chromosomes, Human, Pair 20 | Infant, Newborn | Genetic Linkage | Index Medicus
Journal Article
HUMAN GENETICS, ISSN 0340-6717, 02/1997, Volume 99, Issue 2, pp. 233 - 236
Human hepatocyte nuclear factor 4 (hHNF-4) is a member of the nuclear hormone receptor superfamily and an important transcription factor and developmental... 
EUROGEM | LOCALIZATION | LIVER | GENETICS & HEREDITY | HNF-4 | CHROMOSOME-20 | EXPRESSION | K KM GENETICS & HEREDITY
Journal Article
GENOMICS, ISSN 0888-7543, 11/1994, Volume 24, Issue 1, pp. 172 - 175
The human type 2 cystatins are encoded by a multigene family of eight to nine members. Five functional genes (CST1-CST5) and two pseudogenes (CSTP1 and CSTP2)... 
C AMYLOID ANGIOPATHY | CST3 | CHAIN | MEMBERS | GENETICS & HEREDITY | INSITU HYBRIDIZATION | INHIBITORS | CHROMOSOME-20 | EXPRESSION | FAMILY
Journal Article
Genomics, ISSN 0888-7543, 1992, Volume 12, Issue 1, pp. 69 - 73
Journal Article
Neuroscientist, ISSN 1073-8584, 09/1999, Volume 5, Issue 5, pp. 295 - 301
Idiopathic epilepsies are a heterogenous group of conditions characterized by different types of seizures, ages of onset, and EEG features. By definition,... 
Sodium channel | Potassium channel | Epilepsy | Acetylcholine receptor | epilepsy | FRONTAL-LOBE EPILEPSY | CONFIRMATION | FEBRILE SEIZURES | NEUROSCIENCES | CLINICAL NEUROLOGY | FAMILIAL NEONATAL CONVULSIONS | HETEROGENEITY | acetylcholine receptor | sodium channel | MUTATION | potassium channel | GENERALIZED EPILEPSY | CHROMOSOME-20 | IDIOPATHIC EPILEPSY | SUBUNIT
Journal Article
NEUROPSYCHOPHARMACOLOGY, ISSN 0893-133X, 08/1993, Volume 9, Issue 1, pp. 31 - 40
The authors' goal was to screen for genetic linkage with highly informative deoxyribonucleic acid (DNA) microsatellite markers on a series of moderately sized... 
SEARCH | PSYCHIATRY | POWER | DINUCLEOTIDE REPEAT POLYMORPHISM | SIMULATION | BIPOLAR ILLNESS | NEUROSCIENCES | HUMAN X-LINKED GABA-A RECEPTOR ALPHA-3-SUBUNIT GENE | SUBUNIT GENE GNAS1 | GNAS1 | GENETIC LINKAGE SIMULATIONS | MICROSATELLITES | MAPPING | PHARMACOLOGY & PHARMACY | CHROMOSOME-20 | MAP
Journal Article
Human Genetics, ISSN 0340-6717, 1992, Volume 89, Issue 1, pp. 54 - 58
Benign familial neonatal convulsions (BFNC) is an idiopathic form of epilepsy beginning within the first six months of life. Its genetic origin and autosomal... 
CHROMOSOME-20 | GENETICS & HEREDITY | EPILEPSY | Blotting, Southern | Humans | Infant | Male | Lod Score | Pedigree | Seizures, Febrile - genetics | DNA Probes - genetics | Epilepsy - genetics | Female | Genetic Linkage - genetics | Chromosomes, Human, Pair 20 | Infant, Newborn | epilepsy | D20S19 locus | D20S20 locus | loci | man | linkage analysis | Index Medicus
Journal Article
Journal Article
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