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ELIZABETH SCHORRY, M.D.
M.D.
NPI: 1861423204IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
35.052498(OH)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
UNIVERSITY OF MICHIGAN MEDICAL SCHOOL
Class of 1982
Research & Publications (18)
Genotype-phenotype correlations in Rubinstein-Taybi syndrome.
PMID 18792986·Am J Med Genet A·2008
8-other
Valproate embryopathy: clinical and cognitive profile in 5 siblings.
PMID 15669094·Am J Med Genet A·2005
5-case
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping.
PMID 19557438·Hum Genet·2009
5-case
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography.
PMID 19118659·Bone·2009
8-other
Parental distress, family functioning, and social support in families with and without a child with neurofibromatosis 1.
PMID 17905803·J Pediatr Psychol·2008
8-other
Social, emotional, and behavioral functioning of children with NF1.
PMID 17726688·Am J Med Genet A·2007
8-other
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.
PMID 17666887·Genet Med·2007
6-review
A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature.
PMID 17219392·Am J Med Genet A·2007
5-case
Skeletal demineralization and fractures caused by fetal magnesium toxicity.
PMID 16724078·J Perinatol·2006
5-case
Epidemiology of hemimegalencephaly: a case series and review.
PMID 16283674·Am J Med Genet A·2005
5-case
A girl with partial trisomy 12q24.31 inherited from her father and a possible novel syndrome transmitted from her mother.
PMID 16222678·Am J Med Genet A·2005
5-case
Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1.
PMID 15582155·Brain Res Mol Brain Res·2004
8-other
Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome.
PMID 15562430·Ann Neurol·2004
4-observational
Perception of disease severity in adolescents diagnosed with neurofibromatosis type 1.
PMID 15450543·J Adolesc Health·2004
8-other
Increased need for medical interventions in infants with velocardiofacial (deletion 22q11) syndrome.
PMID 10931419·J Pediatr·2000
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
- 3333 BURNET AVE, ML 4006
CINCINNATI, OH 45229 - Phone
- (513) 636-4760
Quick Facts
- NPI
- 1861423204
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 44
- Publications
- 18
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