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MATTHEW BROGHAMMER, DO
DO
Surgery Physician
NPI: 1124038773IndividualAccepts Medicare
Specialties, Licenses & Credentials
CMS Specialties
PrimaryGENERAL SURGERY
Education
OTHER
Class of 1996
Research & Publications (19)
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
PMID 18360688·Int J Mol Med·2008
8-other
Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders.
PMID 16669610·Mol Diagn Ther·2006
8-other
Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background.
PMID 16273303·Int J Mol Med·2005
8-other
Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations.
PMID 15363549·Cancer Lett·2004
8-other
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations.
PMID 15254256·Mol Biol Evol·2004
8-other
Molecular phylogenetics employing modern and ancient DNA.
PMID 12923304·J Appl Genet·2003
7-preclinical
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness.
PMID 12719097·Am J Ophthalmol·2003
5-case
Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa.
PMID 12402343·Hum Mutat·2002
8-other
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
PMID 12111638·Eur J Hum Genet·2002
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
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Contact & Hours
- Address
- 855 MANKATO AVE
WINONA, MN 55987 - Phone
- (507) 454-3680
Quick Facts
- NPI
- 1124038773
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 30
- Publications
- 19
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