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JEAN HERTZ, M.D.
M.D.
Family Medicine Physician
NPI: 1073755153Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Hypocalcified type of amelogenesis imperfecta in a large family: clinical, radiographic, and histological findings, associated dento-facial anomalies, and resulting treatment load.
PMID 19452331·Acta Odontol Scand·2009
4-observational
Ising model for neural data: model quality and approximate methods for extracting functional connectivity.
PMID 19518488·Phys Rev E Stat Nonlin Soft Matter Phys·2009
8-other
Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p.
PMID 19215056·Am J Med Genet A·2009
5-case
Changes in stress and coping from a randomized controlled trial of a three-month stress management intervention.
PMID 19308298·Scand J Work Environ Health·2009
2-rct
A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome.
PMID 18397837·Mol Genet Metab·2008
8-other
Assessing students' learning needs and attitudes: considerations for gerontology curriculum planning.
PMID 19042220·Gerontol Geriatr Educ·2008
8-other
The development of loads of cations, anions, Cd and Pb in precipitation and of atmospheric concentrations of N-components, in Switzerland from 1988 to 2003.
PMID 17562202·Environ Monit Assess·2008
8-other
MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome.
PMID 18616531·Clin Genet·2008
8-other
X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families.
PMID 18510547·Clin Genet·2008
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
- 209 RAND ST
WASHINGTON, MO 63090 - Phone
- (636) 390-2149
Quick Facts
- NPI
- 1073755153
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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