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BRYAN ANGLE, MD
MD
Retina Specialist (Ophthalmology) Physician
NPI: 1457323537IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology Physician
Ophthalmology
Code: 207W00000X
J-1844(TX)
Retina Specialist (Ophthalmology) PhysicianPrimary
Ophthalmology — Retina Specialist
Code: 207WX0107X
J1844(TX)J-1844(TX)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
OTHER
Class of 1991
Research & Publications (12)
Neuroimaging findings in children with rare or novel de novo chromosomal anomalies.
PMID 18302267·Birth Defects Res A Clin Mol Teratol·2008
8-other
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II.
PMID 17977044·Mol Genet Metab·2008
5-case
An 8-month-old boy with cleft palate, microcephaly, developmental delay, and syndactyly. Smith-Lemili-Opitz syndrome.
PMID 17515167·Pediatr Ann·2007
5-case
A 3-day-old infant with a congenital heart defect and hypocalcemia. 22q11 deletion syndrome.
PMID 17515164·Pediatr Ann·2007
5-case
A 4-month-old girl with an enlarged tongue and limb asymmetry. Beckwith-Wiedeman syndrome.
PMID 17515159·Pediatr Ann·2007
5-case
Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency.
PMID 17304052·Genet Med·2007
8-other
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome.
PMID 16685658·Am J Hum Genet·2006
8-other
Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
PMID 12522795·Am J Med Genet A·2003
5-case
Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
PMID 12210328·Am J Med Genet·2002
5-case
Developmental field defects: coming together of associations and sequences during blastogenesis.
PMID 12116204·Am J Med Genet·2002
5-case
Case of partial duplication 2q3 with characteristic phenotype: rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion.
PMID 10748411·Am J Med Genet·2000
5-case
Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review.
PMID 10607952·Am J Med Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 5540 SARATOGA BLVD STE 200
CORPUS CHRISTI, TX 78413 - Phone
- (361) 993-8510
Quick Facts
- NPI
- 1457323537
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 35
- Publications
- 12
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