Balram Gangaram
Pediatrics | Medical Genetics
Ucsf, 550 16th Street
San Francisco, CA 94158
San Francisco, CA 94158
Last Updated: 09/26/2026
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Found 6 publications
Patent ductus arteriosus and coarctation of the aorta in association with PRDM6 variants.
Journal: American journal of medical genetics. Part A
Published: October 11, 2023
Biallelic OTUD6B variants associated with a Kabuki syndrome-like disorder in three siblings: A clinical report and literature review.
Journal: American journal of medical genetics. Part A
Published: September 11, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 03, 2022
Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review.
Journal: European journal of medical genetics
Published: October 22, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.
Journal: American journal of medical genetics. Part A
Published: September 28, 2020
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.
Journal: American journal of human genetics
Published: February 03, 2020
Showing 1-6 of 6
Last Updated: 09/26/2026