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
DOORS syndrome: Phenotype, genotype and comparison with Coffin-Siris syndrome
Mar 2, 2025
—
by
coffinsiris-foundation
←
Previous:
Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay
Next:
Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A
→
