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PAUL WATERS, MD

MD

Family Medicine Physician

NPI: 1730191065Individual

Specialties, Licenses & Credentials

Family Medicine PhysicianPrimary

Family Medicine

Code: 207Q00000X

C23567(CA)

Research & Publications (20)

Identification of cryptic sex chromosomes and isolation of X- and Y-borne genes.
PMID 18629671·Methods Mol Biol·2008
7-preclinical
LINE-1 elements: analysis by fluorescence in-situ hybridization and nucleotide sequences.
PMID 18629670·Methods Mol Biol·2008
7-preclinical
Surgical treatment of carpal and hand injuries in children.
PMID 18399606·Instr Course Lect·2008
6-review
Forearm rebalancing in osteochondromatosis by radioulnar fusion.
PMID 18090828·Tech Hand Up Extrem Surg·2007
8-other
Sex chromosomes of basal placental mammals.
PMID 17602234·Chromosoma·2007
4-observational
Mammalian sex--Origin and evolution of the Y chromosome and SRY.
PMID 17400006·Semin Cell Dev Biol·2007
6-review
Evolutionary history of LINE-1 in the major clades of placental mammals.
PMID 17225861·PLoS One·2007
7-preclinical
Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?
PMID 16182582·Mol Genet Metab·2005
5-case
Autosomal location of genes from the conserved mammalian X in the platypus (Ornithorhynchus anatinus): implications for mammalian sex chromosome evolution.
PMID 15973504·Chromosome Res·2005
7-preclinical
Update on management of pediatric brachial plexus palsy.
PMID 15931025·J Pediatr Orthop B·2005
6-review
LINE-1 distribution in Afrotheria and Xenarthra: implications for understanding the evolution of LINE-1 in eutherian genomes.
PMID 15338236·Chromosoma·2004
7-preclinical
Percutaneous reduction of incipient malunion of phalangeal neck fractures in children.
PMID 15249098·J Hand Surg Am·2004
8-other
A comparison of homologous genes encoding aminopeptidases among bird and human Encephalitozoon hellem isolates and a rabbit E. cuniculi isolate.
PMID 15221463·Parasitol Res·2004
4-observational
Interobserver and intraobserver reliability of therapist-assisted videotaped evaluations of upper-limb hemiplegia.
PMID 15043910·J Hand Surg Am·2004
8-other
Assignment of the thymosin beta 4 X/Y chromosome (TMSB4X/Y) gene to tammar wallaby chromosome 5p by fluorescence in situ hybridisation.
PMID 15008146·Cytogenet Genome Res·2003
7-preclinical
How PAH gene mutations cause hyper-phenylalaninemia and why mechanism matters: insights from in vitro expression.
PMID 12655545·Hum Mutat·2003
6-review
Assignment of the protocadherin 20 (PCDH20) gene to tammar wallaby chromosome 6q by fluorescence in situ hybridisation.
PMID 12826763·Cytogenet Genome Res·2002
7-preclinical
Assignment of the SMARCF1 gene to tammar wallaby chromosome 5q by fluorescence in situ hybridisation.
PMID 11528131·Cytogenet Cell Genet·2001
7-preclinical
Degradation of mutant proteins, underlying "loss of function" phenotypes, plays a major role in genetic disease.
PMID 11488412·Curr Issues Mol Biol·2001
6-review
Homomeric and heteromeric interactions between wild-type and mutant phenylalanine hydroxylase subunits: evaluation of two-hybrid approaches for functional analysis of mutations causing hyperphenylalaninemia.
PMID 11461190·Mol Genet Metab·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
782 E HARDING WAY
STOCKTON, CA 95204

Location

Practice Location

782 E HARDING WAY, STOCKTON, CA
(209) 475-5500

Quick Facts

NPI
1730191065
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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