Biochemistry, Genetics and Molecular Biology
Lod Score
100%
Gene Linkage
99%
X Chromosome
95%
Linkage Analysis
85%
Genetics
71%
Pedigree
67%
Gene Location
64%
Body Height
43%
Dysplasia
39%
Genetic Marker
38%
Genetic Linkage
37%
Cytogenetics
36%
Gene Mapping
33%
Recombinant
29%
PstI
29%
Genetic Recombination
28%
Missense Mutation
25%
Dinucleotide Repeat
24%
Microsatellite Marker
23%
Obligate Carrier
21%
X Chromosomal Inheritance
19%
RYR1
19%
DNA Probe
19%
Genetic Heterogeneity
19%
Gene Locus
19%
Protein Sequencing
19%
Shotgun Sequencing
19%
Restriction Digest
19%
Centromere
17%
Dystrophin
16%
Exon
16%
PKD1
14%
Chromosome 16
14%
FMR1
13%
Fibroblast
13%
Allele
11%
Stop Codon
11%
X-Inactivation
11%
Open Reading Frame
11%
Alternative Splicing
10%
Orthology
10%
Androgen Receptor
10%
Mental Retardation
9%
Genetic Carrier
9%
Genetic Divergence
9%
Heterozygote
9%
Phenotypic Variation
9%
RNA Splicing
9%
Autosome
9%
Cardiolipin
9%
Neuroscience
X Linked Mental Retardation
79%
Gene Location
39%
Muscle Disorder
38%
X Chromosome
33%
Myotonic Dystrophy
29%
Dilated Cardiomyopathy
29%
Genetic Recombination
27%
Cytogenetics
19%
Chromosome 16
19%
RYR1
19%
Myocardial Disease
19%
Mental Retardation Malformation Syndrome
14%
Endocardial Fibroelastosis
14%
Gene Locus
9%
Amino Terminal Sequence
9%
Alternative Splicing
9%
C-Terminus
9%
Skeletal Muscle
9%
Cardiolipin
9%
Guanine Nucleotide Dissociation Inhibitor
9%
Open Reading Frame
9%
Genetic Mapping
9%
Microcephaly
9%
Unstable DNA Sequence
9%
Apolipoprotein C2
9%
Fragile X Syndrome
9%
Human Chromosome
9%
Muscular Dystrophy
9%
Centromere
9%
Behavior (Neuroscience)
9%
Stop Codon
9%
Hypotonia
9%
Amyloidosis
9%
Protein Sequencing
9%
Missense Mutation
9%
Fibroblast
9%
Microsatellite
9%
Restriction Fragment Length Polymorphism
9%
Shotgun Sequencing
9%
Dinucleotide Repeat
7%
Dystrophin
7%
Medicine and Dentistry
Barth Syndrome
29%
X Linked Mental Retardation
29%
Prenatal Diagnosis
24%
Gene Linkage
23%
Linkage Analysis
20%
Dilated Cardiomyopathy
19%
X Chromosomal Inheritance
19%
Gynecomastia
14%
Diseases
14%
Myocardial Disease
13%
Genetic Linkage
13%
Chromosome 16
12%
Arm
12%
Molecular Diagnosis
9%
Lymphoproliferative Disease
9%
Human Chromosome
9%
Duchenne Muscular Dystrophy
9%
Becker Muscular Dystrophy
9%
Pigmentary Disorder
9%
Amyloidosis
9%
Finger
9%
Prenatal Disease
9%
Zinc Finger Protein
9%
Developmental Disorder
9%
Hypotonia
9%
Heterozygote Detection
9%
Spondyloepiphyseal Dysplasia
9%
Centromere
9%
RNA Splicing
9%
Restriction Fragment Length Polymorphism
9%
Biopsy Technique
9%
Short Stature
9%
Neutropenia
7%
Myopathy
7%
Pedigree
6%
Protein Sequencing
6%
Sequence Analysis
6%
Infancy
6%
Obligate Carrier
6%
X Chromosome
6%