Keyphrases
Adult Form
9%
Amniotic Fluid Cells
8%
Ashkenazi
23%
Ashkenazi Jews
40%
Association Study
8%
Bipolar Disorder
21%
CAG Repeat
12%
Charcot-Marie-Tooth Disease
8%
Compound Heterozygous mutation
16%
Cultured Skin
12%
Duplication
8%
Fetus
18%
Fibroblasts
10%
Gangliosides
12%
Gangliosidosis
18%
Genotype
15%
GM2 Gangliosidosis
33%
Haplotype Analysis
10%
Heat-labile
12%
HEXA Gene
14%
Hexosaminidase A
90%
Hexosaminidase B
20%
Isozymes
10%
Israeli
23%
Jewish
18%
Jewish Family
11%
Jewish Patients
13%
Jewish Population
14%
KCNN3
12%
Late Infantile
8%
Late-onset
14%
Leukocytes
14%
Moroccan
14%
Moroccan Jews
10%
New mutation
12%
Point mutation
9%
Polymorphism
8%
Prenatal Diagnosis
10%
Pyrimethamine
8%
Quantitative PCR
8%
Schizophrenia
41%
Schizophrenia Symptoms
10%
Schizophrenic Patients
18%
Skin Fibroblasts
13%
Spinal muscular Atrophy
16%
Sulforhodamine 101
8%
Tay-Sachs
52%
Tay-Sachs Disease
74%
β-hexosaminidase
44%
β-N-acetylhexosaminidase
8%
Biochemistry, Genetics and Molecular Biology
Adrenergic Receptor
6%
Allele
30%
Codon
10%
Compound Heterozygosity
7%
Eicosanoid Receptor
6%
Enzyme
15%
Exon
21%
Exon Skipping
6%
Fibroblast
23%
Ganglioside
16%
Gangliosidosis
12%
Genetics
16%
Genotyping
6%
GM1
8%
GM2 Gangliosidoses
32%
Haplotype
10%
HEXA
29%
Hexosaminidase
100%
Homozygote
7%
Immunodiffusion
5%
Isozyme
8%
Leukocyte
12%
Point Mutation
9%
Precursor
6%
Prevalence
6%
Real-Time Polymerase Chain Reaction
6%
Tay-Sachs Disease
84%
