Home
Search
About
Contact
The Genetics Corner: DiGeorge Anomaly Associated with Diabetic Embryopathy in an Infant without a Deletion on Chromosome 22q11
September 30, 2020
/
Cardiology
,
Case Report
,
Genetic
,
Immunology/Rheumatology
,
Medical Practices
,
Testing
Subhadra Ramanathan MS, MSc, Robin Dawn Clark MD
nt-20-09-095-097
Download
←
Previous:
Perinatal/Neonatal Medico-Legal Forum: Valpractice
Next:
Interpreting Umbilical Cord Blood Gases: Cord Occlusion with Terminal Fetal Bradycardia: Part 1
→