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Keyphrases
Estriol
100%
New mutation
100%
Triple Marker
100%
Isolated Adrenocorticotropic Hormone Deficiency
100%
Adrenocorticotropic Hormone
40%
Neonatal Death
40%
Smith-Lemli-Opitz Syndrome
40%
Etiology
20%
Early Postnatal
20%
Dehydroepiandrosterone Sulfate (DHEAS)
20%
5′-end
20%
Postnatal Day
20%
Pregnant Women
20%
Early Diagnosis
20%
Stress Management
20%
Pituitary
20%
Human Chorionic Gonadotropin
20%
Tertiary Care Hospital
20%
Autosomal Recessive
20%
Prenatal Diagnosis
20%
Geneticists
20%
Splice Site
20%
Down Syndrome
20%
Nonsense mutation
20%
Normal Development
20%
Terminal Differentiation
20%
Cardiomyopathy
20%
Stop Codon
20%
Molecular Analysis
20%
Multidisciplinary Team
20%
Fetal Death
20%
Gain-of-function mutation
20%
Normal Growth
20%
First Cousin
20%
Fetal Growth
20%
Hormone Levels
20%
Maintenance Dose
20%
Nonsense-mediated mRNA Decay
20%
Pediatric Endocrinologist
20%
Alpha-fetoprotein
20%
Rare Cause
20%
Fetal Ultrasound
20%
Stress Dose
20%
Pituitary Function
20%
Postnatal Diagnosis
20%
Steroidogenesis
20%
Corticotroph
20%
Glucocorticoid Therapy
20%
Hydrocortisone
20%
Sulfatase
20%
Placental Perfusion
20%
Steroid Sulfatase
20%
X-linked Ichthyosis
20%
Unconjugated Estriol
20%
Fetal Sonography
20%
Adrenal Insufficiency
20%
Open Neural Tube Defect
20%
Cortisol Hormone
20%
Serum Analytes
20%
Adrenocortical Insufficiency
20%
Addisonian Crisis
20%
7-ketocholesterol
20%
Hypoglycemic Seizures
20%
T-box Transcription Factors
20%
Medicine and Dentistry
Corticotropin
100%
Hormone Deficiency
100%
Estriol
100%
Newborn Death
33%
Hydrocortisone
33%
Fetus Echography
33%
Smith-Lemli-Opitz Syndrome
33%
Adrenal Crisis
33%
Epileptic Seizure
16%
Chorionic Gonadotropin
16%
Echography
16%
Down Syndrome
16%
Autosomal Recessive Inheritance
16%
Karyotype
16%
Antidiabetic Agent
16%
Myocardial Disease
16%
Fetus Death
16%
Growth, Development and Aging
16%
Prenatal Diagnosis
16%
Glucocorticoid
16%
Early Diagnosis
16%
Intron
16%
Nonsense Mutation
16%
Fetus Growth
16%
Hypophysis Function
16%
Hormone Determination
16%
Pediatric Endocrinologist
16%
Stop Codon
16%
Loss of Function Mutation
16%
Nonsense Mediated mRNA Decay
16%
Prasterone Sulfate
16%
Steroidogenesis
16%
Adrenal Insufficiency
16%
Neural Tube Defect
16%
Fetoprotein
16%
Maintenance Drug Dose
16%
Steroid Sulfatase
16%
X-Linked Ichthyosis
16%
T Box Transcription Factor
16%
Sulfatase
16%
7 Dehydrocholesterol
16%
Handling Stress
16%
Diseases
16%
Biochemistry, Genetics and Molecular Biology
Adrenocorticotropic Hormone
100%
Cortisol
50%
Karyotype
25%
Intron
25%
Human Chorionic Gonadotropin
25%
Autosomal Recessive Inheritance
25%
Stop Codon
25%
Down Syndrome
25%
Nonsense Mutation
25%
Perfusion
25%
Growth, Development and Aging
25%
Loss of Function Mutation
25%
Neural Tube
25%
Maintenance Drug Dose
25%
Nonsense-Mediated Decay
25%
Steroid Biosynthesis
25%
Steroid Sulfatase
25%
T Box Transcription Factor
25%
Sulfatase
25%
7-Dehydrocholesterol
25%
Hypophysis Function
25%
Glucocorticoid
25%
Dehydroepiandrosterone Sulfate
25%
Handling Stress
25%