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Annals of the New York Academy of Sciences, ISSN 0077-8923, 1991, Volume 642, Issue 1, pp. 419 - 430
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
Journal Article
Genomics, ISSN 0888-7543, 1992, Volume 12, Issue 1, pp. 69 - 73
Journal Article
ANNALS OF HUMAN GENETICS, ISSN 0003-4800, 01/1992, Volume 56, pp. 35 - 43
Red blood cell S-adenosylhomocysteine hydrolase (AHCY) from individuals of 1, 2-1 and 3-1 phenotypes was partially purified and K(m) and V(max) determined in... 
DEAMINASE | L-HOMOCYSTEINE HYDROLASE | MECHANISM | GENETICS & HEREDITY | ADENOSYL-L-HOMOCYSTEINE | HUMAN GENES | POLYMORPHISM | CHROMOSOME-20
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
American Journal of Medical Genetics, ISSN 0148-7299, 1993, Volume 45, Issue 1, pp. 14 - 16
Journal Article
CLINICAL GENETICS, ISSN 0009-9163, 07/1993, Volume 44, Issue 1, pp. 26 - 31
A ring chromosome 20 in a male infant with epileptic seizures, mental and somatic growth retardation, and behavioural disturbances is described. Conventional... 
TELOMERIC SEQUENCES | ANOMALIES | RESOLUTION | GENETICS & HEREDITY | SYNDROME | CHROMOSOME-20 | CHILD | PRIMED IN-SITU LABELING | RING CHROMOSOME | MOSAICISM
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
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
Journal Article
AMERICAN JOURNAL OF HUMAN GENETICS, ISSN 0002-9297, 08/1994, Volume 55, Issue 2, pp. 238 - 243
Alagille syndrome is a clinically defined, dominantly inherited disorder affecting the liver, heart, face, eye, and vertebrae. Alagille syndrome has previously... 
LINKAGE MAP | 20P | GENE | ARTERIOHEPATIC DYSPLASIA | GENETICS & HEREDITY | MARKERS | NEUROFIBROMATOSIS | CHROMOSOME-20 | ARM | DELETION
Journal Article
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