Roopa L. Nalam

Internal Medicine
One Baylor Plz
Ste NC100 BCM MS 621
Houston, TX 77030

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 1 publications

De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.

De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.

Journal: American journal of human genetics
Published: February 02, 2014
Showing 1-1 of 1

Last Updated: 09/26/2026