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KATHLEEN LEPPIG, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1427007962IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
MD00026782(WA)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Education
CLVLND CLINIC LERNER COLLEGE OF MED OF CASE WSTN RSV UNIVERSITY
Class of 1986
Research & Publications (14)
Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
PMID 11480912·Semin Reprod Med·2001
6-review
Familial cryptic (20;21) translocation identified by in situ hybridization technologies.
PMID 10946352·Am J Med Genet·2000
5-case
Motivating factors for physician ordering of factor V Leiden genetic tests.
PMID 19139326·Arch Intern Med·2009
4-observational
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
PMID 18642388·Hum Mutat·2008
8-other
Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.
PMID 16690971·Blood·2006
8-other
Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.
PMID 16463420·Birth Defects Res A Clin Mol Teratol·2006
5-case
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
PMID 16141010·J Med Genet·2005
5-case
Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.
PMID 15959648·J Genet Couns·2005
6-review
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
PMID 15739154·Am J Hum Genet·2005
8-other
Sacral hemangioblastoma in a patient with von Hippel-Lindau disease. Case report and review of the literature.
PMID 15350042·Neurosurg Focus·2003
5-case
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.
PMID 12410200·J Pediatr·2002
5-case
Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?
PMID 11857550·Am J Med Genet·2002
8-other
The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome.
PMID 11332402·J Med Genet·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 201 16TH AVE E
SEATTLE, WA 98112 - Phone
- (206) 326-3000
Quick Facts
- NPI
- 1427007962
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 40
- Publications
- 14
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