Biochemistry, Genetics and Molecular Biology
Allele
100%
Phenylketonuria
77%
Genetic Divergence
58%
Newborn Screening
58%
Exon
51%
Screening
48%
Genotyping
45%
Genetic Screening
45%
Haplotype
38%
Genetic Variation
38%
Restriction Fragment Length Polymorphism
33%
Genetic Risk
29%
Chromosomal Abnormalities
29%
Phenylalanine
27%
Proband
23%
GSTT1
23%
Genetic Marker
22%
Medical Record
22%
Prevalence
22%
Patient Compliance
20%
Gene Mutation
19%
Biotinidase
19%
Minigene
19%
Gene Polymorphism
19%
Autosomal Recessive Disorder
19%
Skeletal Muscle
19%
Leigh's Disease
19%
Gamma-Glutamyl Transpeptidase
19%
Single-Nucleotide Polymorphism
19%
Survival Rate
19%
Precursor
19%
Immunoreactive Trypsinogen
19%
Cystic Fibrosis
19%
B Cell
19%
Ornithine Transcarbamylase Deficiency
19%
IL1B
19%
Event Free Survival
19%
SMN1
19%
Microdeletion Syndrome
19%
Polymerase Chain Reaction
19%
Karyotype
19%
GSTP1
19%
Alkaline Phosphatase
19%
Copper Metabolism
19%
PTPN11
19%
Progeny
19%
Chromosomal Translocation
19%
Karyotyping
19%
First Trimester Pregnancy
19%
Multiplex Ligation-Dependent Probe Amplification
17%
Medicine and Dentistry
Phenylketonuria
97%
Spinal Muscular Atrophy
58%
Diagnosis
45%
Screening
42%
Newborn Screening
41%
Disease
39%
Genetic Disorder
27%
Prenatal Diagnostics
23%
Enzyme Activity
21%
Nuchal Translucency Measurement
21%
B Cell
19%
Crigler-Najjar Syndrome
19%
Clinical Management
19%
Patient Referral
19%
Leigh's Disease
19%
Liver Disease
19%
Chronic Hepatitis C
19%
Insulin Dependent Diabetes Mellitus
19%
Periodontitis
19%
Latent Tuberculosis
19%
Hurler Syndrome
19%
Brain Abnormalities
19%
Bilirubin
19%
Sweat Test
19%
X-Linked Lymphoproliferative Disease
19%
Enzyme Replacement Therapy
19%
Cystic Fibrosis
19%
CD3 Antigen
19%
Lymphocyte
19%
Malignant Neoplasm
19%
Noonan Syndrome
19%
Lymphocyte Subpopulation
19%
Seasonal Variation
19%
Natural Killer Cell
17%
Case Presentation
16%
Immune Deficiency
16%
Magnetic Resonance Imaging
15%
Phenylalanine
14%
Immunoreactive Trypsinogen
13%
Neuronal Migration Disorder
12%
T Cell
12%
Infection
12%
Karyotype
11%
Neonates
11%
Dental Caries
10%
Gene Mutation
9%
Prenatal Diagnosis
9%
Crigler Najjar Syndrome Type I
9%
Gilbert's Syndrome
9%
Hyperbilirubinemia
9%
