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DAVID TOMKINS, M.D.
M.D.
Family Medicine Physician
NPI: 1891058962IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
A136310(CA)MT202195(PA)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2012
Research & Publications (14)
Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay.
PMID 11896455·Eur J Hum Genet·2002
5-case
An investigation of the role of 5-HT(2C) receptors in modifying ethanol self-administration behaviour.
PMID 11888565·Pharmacol Biochem Behav·2002
7-preclinical
Addiction and the brain: the role of neurotransmitters in the cause and treatment of drug dependence.
PMID 11276551·CMAJ·2001
6-review
Effect of 5-HT(1B) receptor ligands on self-administration of ethanol in an operant procedure in rats.
PMID 10837852·Pharmacol Biochem Behav·2000
7-preclinical
Brief hypnosis for severe needle phobia using switch-wire imagery in a 5-year old.
PMID 17596226·Paediatr Anaesth·2007
5-case
Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells.
PMID 15887093·Am J Hum Genet·2005
8-other
Motor impairing effects of ethanol and diazepam in rats selectively bred for high and low ethanol consumption in a limited-access paradigm.
PMID 15608597·Alcohol Clin Exp Res·2004
4-observational
Diploid/tetraploid/t(1;6) mosaicism in a 17-year-old female with hypomelanosis of Ito, multiple congenital anomalies, and body asymmetry.
PMID 12239727·Am J Med Genet·2002
5-case
Maternal cell contamination of amniotic fluid samples obtained by open needle versus trocar technique of amniocentesis.
PMID 12196873·J Obstet Gynaecol Can·2002
4-observational
Health-related quality-of-life assessment of prenatal diagnosis: chorionic villi sampling and amniocentesis.
PMID 12180075·Genet Test·2002
3-trial
Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat.
PMID 11113905·Prenat Diagn·2000
5-case
Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group.
PMID 10925387·Am J Med Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 635 ANDERSON RD, SUITE 12
DAVIS, CA 95616 - Phone
- (530) 758-1122
Quick Facts
- NPI
- 1891058962
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 14
- Publications
- 14
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