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PAUL MACLEOD, MD
MD
Orthopaedic Surgery Physician
NPI: 1982796314Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
6386(ND)
Research & Publications (20)
Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients.
PMID 19213033·Am J Med Genet A·2009
8-other
Perinatal lethal Gaucher's disease without prenatal complications.
PMID 18070135·Clin Genet·2008
5-case
Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.
PMID 19000322·Mol Cytogenet·2008
8-other
Inverted duplication with terminal deletion of 5p and no cat-like cry.
PMID 18266247·Am J Med Genet A·2008
5-case
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
PMID 17160902·Am J Hum Genet·2007
7-preclinical
The impact of prenatal diagnosis on neural tube defect (NTD) pregnancy versus birth incidence in British Columbia.
PMID 16682757·J Appl Genet·2006
8-other
Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2.
PMID 16155192·J Med Genet·2006
5-case
Clinical stringency greatly improves mutation detection in Rett syndrome.
PMID 16225173·Can J Neurol Sci·2005
8-other
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
PMID 15739154·Am J Hum Genet·2005
8-other
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.
PMID 15034579·Nat Genet·2004
8-other
Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria.
PMID 15235021·J Med Genet·2004
4-observational
Phase II study of alternating chemotherapy regimens for advanced non-small cell lung cancer.
PMID 15084389·Lung Cancer·2004
3-trial
Ultrathin needle (25 G) aspiration lung biopsy: diagnostic accuracy and complication rates.
PMID 14551726·Eur Radiol·2004
6-review
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD.
PMID 12955766·Am J Med Genet A·2003
8-other
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
PMID 12786753·Clin Genet·2003
8-other
Rett syndrome: investigation of nine patients, including PET scan.
PMID 12463490·Can J Neurol Sci·2002
8-other
[Prophylactic gastrectomy in patients with deleterious E-cadherin gene mutation].
PMID 11852408·Gastroenterol Clin Biol·2001
8-other
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia.
PMID 11595021·Clin Genet·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
- 101 3RD AVE SW
MINOT, ND 58701 - Phone
- (701) 857-5986
Quick Facts
- NPI
- 1982796314
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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