Genomic Screening, New Gene Associations

ESPE Yearbook of Paediatric Endocrinology

ISSN 1662-4009 (online)

An indispensable reference tool endorsed by the European Society for Paediatric Endocrinology

Previous issue | Volume 22 | ESPEYB25

Yearbook of Paediatric Endocrinology 2025

2. Antenatal and Neonatal Endocrinology

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Rare Syndromes

Table of contents

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Hyperinsulinemic Hypoglycemia, Neonatal Diabetes

ey0022.2-7 | Genomic Screening, New Gene Associations

2.7. Population-based, first-tier genomic newborn screening in the maternity ward

ey0022.2-8 | Genomic Screening, New Gene Associations

2.8. Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

ey0022.2-9 | Genomic Screening, New Gene Associations

2.9. Sex dimorphic associations of Prader-Willi imprinted gene expressions in umbilical cord with prenatal and postnatal growth in healthy infants

ESPE Yearbook of Paediatric Endocrinology
ISSN 1662-4009 (Online)
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