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CAROLINE MELDRUM, M.D.
M.D.
Pediatrics Physician
NPI: 1245679919Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
4301103236(MI)
Research & Publications (20)
MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.
PMID 19156174·Eur J Hum Genet·2009
4-observational
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.
PMID 19372674·Cytogenet Genome Res·2009
5-case
Albumin use guidelines and outcome in a surgical intensive care unit.
PMID 18936370·Arch Surg·2008
8-other
Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c-KIT.
PMID 18795925·Br J Dermatol·2008
8-other
Whole genome amplification and its impact on CGH array profiles.
PMID 18710509·BMC Res Notes·2008
8-other
IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer.
PMID 18623088·Int J Cancer·2008
8-other
Multidisciplinary care of the patient with chronic obstructive pulmonary disease.
PMID 18453373·Proc Am Thorac Soc·2008
6-review
The -149C>T SNP within the DeltaDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer.
PMID 18336997·Cancer Lett·2008
8-other
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
PMID 18252223·Am J Hum Genet·2008
8-other
Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.
PMID 18027856·Int J Cancer·2008
8-other
Spinal muscular atrophy genetic counseling access and genetic knowledge: parents' perspectives.
PMID 17761658·J Child Neurol·2007
8-other
Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer.
PMID 17454884·Scand J Gastroenterol·2007
4-observational
MDM2 SNP309 T>G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients.
PMID 17096342·Int J Cancer·2007
8-other
Genetic polymorphisms in xenobiotic clearance genes and their influence on disease expression in hereditary nonpolyposis colorectal cancer patients.
PMID 17119063·Cancer Epidemiol Biomarkers Prev·2006
8-other
Re: IGF-1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer.
PMID 17105989·J Natl Cancer Inst·2006
8-other
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
PMID 17026623·Clin Genet·2006
8-other
Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.
PMID 16353134·Int J Cancer·2006
8-other
Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations.
PMID 15761860·Int J Cancer·2005
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
- 26850 PROVIDENCE PKWY, SUITE 455
NOVI, MI 48374 - Phone
- (248) 465-4847
Quick Facts
- NPI
- 1245679919
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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