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JARED JON LIEBELT M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1922448299IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
036142878(IL)
Education
OTHER
Class of 2013
Research & Publications (14)
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.
PMID 19372674·Cytogenet Genome Res·2009
5-case
Mitochondrial fatty acid transport enzyme deficiency--implications for in vitro fertilization.
PMID 19362304·Fertil Steril·2009
5-case
A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family.
PMID 19291767·Am J Med Genet A·2009
5-case
Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication.
PMID 18076674·Clin Genet·2008
5-case
Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling.
PMID 18925618·Prenat Diagn·2008
8-other
Preimplantation genetic diagnosis for BRCA1 exon 13 duplication mutation using linked polymorphic markers resulting in a live birth.
PMID 18302307·Prenat Diagn·2008
5-case
Nail-patella syndrome and its association with glaucoma: a review of eight families.
PMID 16825280·Br J Ophthalmol·2006
8-other
Singleton births after routine preimplantation genetic diagnosis using exclusion testing (D4S43 and D4S126) for Huntington's disease.
PMID 16500325·Fertil Steril·2006
8-other
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome.
PMID 15805156·J Med Genet·2005
8-other
Tacrolimus and cerivastatin pharmacokinetics and adverse effects after single and multiple dosing with cerivastatin in renal transplant recipients.
PMID 12895195·Br J Clin Pharmacol·2003
3-trial
Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition.
PMID 12868473·Clin Dysmorphol·2003
5-case
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum.
PMID 12833403·Am J Med Genet A·2003
5-case
An evidence-based specialist breast nurse role in practice: a multicentre implementation study.
PMID 12641561·Eur J Cancer Care (Engl)·2003
4-observational
Pre-conception and antenatal screening for the fragile site on the X-chromosome.
PMID 11869607·Cochrane Database Syst Rev·2002
1-meta
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2150 PFINGSTEN RD STE 1200
GLENVIEW, IL 60026 - Phone
- (847) 864-3278
Quick Facts
- NPI
- 1922448299
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 14
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