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For Patients:
To request an appointment, call 800.678.KIDS (5437) or fill out our online form.

For Referring Physicians:
To refer a patient, call Children's Direct at 800.678.HELP (4357).

Beth A Kozel, MD

Dr. Kozel focuses her practice on genetics. She sees children with inherited medical conditions and multiple congenital anomalies. She has a clinical and research interest in the genetics of Williams Syndrome, familial supravalvular aortic stenosis and cutis laxa.

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Services: Genetics and Genomic Medicine, Williams Syndrome Center

Practice Name: Genetics And Genomic Medicine

Age: 39

Gender: Female

In Area Since: 2009

In Practice Since: 2009

Specialties:

Genetics-Pediatric - certified
*Pediatrics - certified

Hospitals:

Barnes-Jewish Hospital
St. Louis Children's Hospital

Academic Profile:

Washington University School of Medicine

For Patients:
To request an appointment, call 800.678.KIDS (5437) or fill out our online form.

For Referring Physicians:
To refer a patient, call Children's Direct at 800.678.HELP (4357).

Public transportation available | Handicap accessible

One Children's Place
Suite 2D
Saint Louis, MO 63110
314.454.6093

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Education

Medical School: Washington University School of Medicine St. Louis
Internship: St. Louis Children's Hospital
Residency: St. Louis Children's Hospital
Fellowship: Washington University School of Medicine St. Louis

Health Plans Accepted

Aetna HMO/Open Access	Aetna Managed Choice POS
Aetna Medicare HMO	Aetna Medicare Open Access (HMO/POS
Aetna Medicare PPO	Aetna POS/PPO/Choice
Aetna PPO	Anthem BCBS Blue Access Choice PPO
Anthem BCBS Blue Access PPO	Anthem BCBS Blue Preferred HMO/POS
BCBS of IL HMO	BCBS of IL PPO
Beech Street/Capp Care PPO	Best Doctors Inc
Cigna Open Access HMO/POS	Cigna PPO
Community Care Network PPO	Coventry Advantra HMO - Medicare
Coventry ASO	Coventry Gold Advantage- Medicare
Coventry HMO/POS	Coventry PPO
Essence Standard/Enhanced	First Health
Great-West HMO/POS	Great-West Open Access
Great-West PPO	Health Alliance HMO & PPO
HealthCare USA MC+	Healthlink Open Access/HMO/POS
Healthlink PPO	HFN Inc. PPO
Home State-MC+	Humana Gold Choice PFFS - Medicare
Humana Gold Plus HMO - Medicare	Humana POS-Medicare
Humana PPO/ChoiceCare Network	HumanaChoice PPO-Medicare
Medicaid MO/ Missouri HealthNet	Medicare
Mercy Health Plan HMO/POS	Mercy Health Plan PPO
MO Medicaid Secondary to Medicare	MultiPlan PPO
Primrose Tertiary/Quarternary	Private Health Care Systems PPO
Tricare/Triwest Prime HMO/POS	Tricare/Triwest Standard/ Extra PPO
Union Pacific RR Emp. Health System	United HC MCARE Complete Choice PPO
United HC MCARE Complete HMO	United HC MCARE CompleteEssen. HMO
United HC MCARE Dual Complete	United Healthcare Choice/Choice+
United Healthcare PPO/ Options	United Healthcare Select/Select+POS
USA Managed Care Org	Verify insurance with office
Worker's Compensation

Genetic modifiers of the cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic Noncomplementation.Kozel BA, Knutsen RH, Ye L, Ciliberto CH, Broekelmann TJ, Mecham RP.J Biol Chem. 2011 Nov 2. [Epub ahead of print]

PMID:: 22049077; [PubMed - as supplied by publisher]

Free Article Related citations BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome.Reis LM, Tyler RC, Schilter KF, Abdul-Rahman O, Innis JW, Kozel BA, Schneider AS, Bardakjian TM, Lose EJ, Martin DM, Broeckel U, Semina EV.Hum Genet. 2011 Oct;130(4):495-504. Epub 2011 Feb 22.

PMID:: 21340693; [PubMed - indexed for MEDLINE]

Free PMC Article Related citations Distinct clinical and histopathological presentations of Danon cardiomyopathy in young women.Toib A, Grange DK, Kozel BA, Ewald GA, White FV, Canter CE.J Am Coll Cardiol. 2010 Jan 26;55(4):408-10. No abstract available.

PMID:: 20117447; [PubMed - indexed for MEDLINE]

Related citations Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, Kozel BA, Sparagana S, Roeder ER, McGrew SG, Kurczynski TW, Allison LJ, Amato S, Savage S, Patel A, Stankiewicz P, Beaudet AL, Cheung SW, Lupski JR.J Med Genet. 2010 May;47(5):332-41. Epub 2009 Nov 12.