Search

Your search keyword '"Deardorff, Matthew A."' showing total 8 results

Search Constraints

Start Over You searched for: Author "Deardorff, Matthew A." Remove constraint Author: "Deardorff, Matthew A." Publication Year Range This year Remove constraint Publication Year Range: This year
8 results on '"Deardorff, Matthew A."'

Search Results

1. Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

2. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

3. Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders.

4. Increased Expression ofZFPM2BypassesSRYto Drive 46,XX Testicular Development: A New Mechanism of 46,XX DSD

7. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

8. 44. UMI-based expanded NGS panel in precision molecular diagnosis of vascular anomalies: Early results.

Catalog

Books, media, physical & digital resources