Donate
Facebook
Instagram
Mail
New Diagnosis
Research
Engage
Media
Advocacy
Conference
2025 Conference
Past Conferences
2024 Conference
2023 Conference
2022 Conference
2021 Conference
Board of Directors
Emily’s Fund
In Memory
Growth Hormone Deficiency due to p.(GIn467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome
Sep 25, 2024
—
by
coffinsirisdev
←
Previous:
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia
Next:
Consolidation of the clinical and genetic definition of a SOX4-related neurodevelopmental syndrome
→
