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Frühzeitige Ovarialinsuffizienz und FMR1-Mutation
Translated title of the contribution
:
Premature ovarian insufficiency (POI) und FMR1 mutation
A. Schröer
*
*
Corresponding author for this work
Clinic of Gynecology and Obstetrics
Overview
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Dive into the research topics of 'Premature ovarian insufficiency (POI) und FMR1 mutation'. Together they form a unique fingerprint.
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Biochemistry, Genetics and Molecular Biology
Premutation
100%
Allele
100%
Untranslated Region
50%
X Chromosome
50%
Keyphrases
Premature Ovarian Insufficiency
100%
FX-associated Primary Ovarian Insufficiency (FXPOI)
20%
Repeat Region
20%
Variable Phenotype
20%
Menopause Onset
20%
Premutation Alleles
20%
Full mutation
20%
INIS
menopause
16%