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STEVEN BLEYL, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1467405407Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

5400608-1205(UT)
Pediatrics Physician

Pediatrics

Code: 208000000X

5400608-1205(UT)

Research & Publications (7)

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes.
PMID 17994562·Am J Med Genet A·2007
5-case
Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients.
PMID 17568391·Eur J Hum Genet·2007
7-preclinical
Analysis of a Scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12.
PMID 17036341·Am J Med Genet A·2006
8-other
Two unique patients with novel microdeletions in 4p16.3 that exclude the WHS critical regions: implications for critical region designation.
PMID 17696124·Am J Med Genet A·2007
5-case
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.
PMID 17431905·Am J Med Genet A·2007
5-case
Restricted expression of Fgf16 within the developing chick inner ear.
PMID 16786592·Dev Dyn·2006
7-preclinical
Vasculogenesis drives pulmonary vascular growth in the developing chick embryo.
PMID 15765515·Dev Dyn·2005
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
100 MARIO CAPECCHI DR
SALT LAKE CITY, UT 84113

Location

Practice Location

100 MARIO CAPECCHI DR, SALT LAKE CITY, UT
(801) 213-3599

Quick Facts

NPI
1467405407
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
7

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