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The History of Prenatal Diagnosis of Congenital Adrenal Hyperplasia
Denesy Mancenido
, Maria I. New
Friedman Brain Institute
Genetics and Genomic Sciences
Icahn School of Medicine at Mount Sinai
Pediatrics
Research output
:
Chapter in Book/Report/Conference proceeding
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Chapter
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peer-review
2
Scopus citations
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Dive into the research topics of 'The History of Prenatal Diagnosis of Congenital Adrenal Hyperplasia'. Together they form a unique fingerprint.
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Biochemistry, Genetics and Molecular Biology
Gene Linkage
100%
First Trimester Pregnancy
100%
Amnion Fluid
100%
21-Hydroxylase
50%
Virilization
50%
Molecular Genetics
50%
17-Hydroxyprogesterone
50%
Steroid Biosynthesis
50%
Pseudogene
50%
Dexamethasone
50%
Polymerase Chain Reaction
50%
Deficiency
50%
Keyphrases
Congenital Adrenal Hyperplasia
100%
Prenatal Diagnosis
100%
Severe Disease
28%
First Trimester
28%
Prenatal Treatment
28%
Amniotic Fluid
28%
Early Detection
14%
Linkage Study
14%
Virilization
14%
21-Hydroxylase Deficiency (21OHD)
14%
Polymerase Chain Reaction
14%
Fetus
14%
17-hydroxyprogesterone (17-OHP)
14%
Reaction-based
14%
Diagnostic Procedures
14%
Increased Safety
14%
External Genitalia
14%
Genital Ambiguity
14%
Adrenal Steroidogenesis
14%
Pseudogene
14%
Molecular Genetic Analysis
14%
Noninvasive Prenatal Diagnosis
14%
CYP21A2 Gene
14%
HLA System
14%
Close Linkage
14%
CYP21A2
14%
CYP21A1P
14%
Medicine and Dentistry
Congenital Adrenal Hyperplasia
100%
Prenatal Diagnosis
100%
Diseases
50%
Gene Linkage
25%
First Trimester Pregnancy
25%
Amnion Fluid
25%
Dexamethasone
12%
Genetic Analysis
12%
Ambiguous Genitalia
12%
Steroid 21 Monooxygenase Deficiency
12%
Virilization
12%
Hydroxyprogesterone
12%
Cloning
12%
Pseudogene
12%
Steroidogenesis
12%
Polymerase Chain Reaction
12%