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MEGAN HILDA BREUNING M.D.
M.D.
Student in an Organized Health Care Education/Training Program
NPI: 1508654344Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations.
PMID 10982965·Am J Med Genet·2000
5-case
[Genetic associate studies in multifactorial genetic diseases].
PMID 19374090·Ned Tijdschr Geneeskd·2009
8-other
[Autosomal dominant polycystic kidney disease: new insights and possible drugs].
PMID 19490717·Ned Tijdschr Geneeskd·2009
6-review
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.
PMID 19409785·Neuromuscul Disord·2009
4-observational
Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathways.
PMID 19401297·Hum Mol Genet·2009
7-preclinical
Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy.
PMID 19475718·Clin Genet·2009
8-other
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
PMID 18550696·J Med Genet·2009
8-other
A flexible route to chiral 2-endo-substituted 9-oxabispidines and their application in the enantioselective oxidation of secondary alcohols.
PMID 19086891·J Org Chem·2009
8-other
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first.
PMID 19436329·Eur J Hum Genet·2009
8-other
Split hand-foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion-evidence for further heterogeneity?
PMID 19353584·Am J Med Genet A·2009
5-case
RNF135 mutations are not present in patients with Sotos syndrome-like features.
PMID 19291764·Am J Med Genet A·2009
8-other
No vessel wall abnormalities in a human foetus with a NOTCH3 mutation.
PMID 18196251·Acta Neuropathol·2008
5-case
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families.
PMID 18981015·Clin Cancer Res·2008
8-other
Identification of copy number variants associated with BPES-like phenotypes.
PMID 18953567·Hum Genet·2008
8-other
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
PMID 18398432·Eur J Hum Genet·2008
8-other
Genetic testing in familial melanoma: uptake and implications.
PMID 18613292·Psychooncology·2008
8-other
Quantification of Cre-mediated recombination by a novel strategy reveals a stable extra-chromosomal deletion-circle in mice.
PMID 18298805·BMC Biotechnol·2008
7-preclinical
Somatic APC mosaicism: an underestimated cause of polyposis coli.
PMID 17604324·Gut·2008
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 501 HOWARD AVENUE, SUITE F4
ALTOONA, PA 16601 - Phone
- (814) 889-2701
Quick Facts
- NPI
- 1508654344
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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