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FREDERICK MACDONALD, PHD MSW
PHD MSW
Clinical Social Worker
NPI: 1275645947Individual
Specialties, Licenses & Credentials
Clinical Social WorkerPrimary
Social Worker — Clinical
Code: 1041C0700X
Research & Publications (20)
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.
PMID 19073614·Hum Reprod·2009
8-other
Contrasting clinical manifestations of SDHB and VHL associated chromaffin tumours.
PMID 19208735·Endocr Relat Cancer·2009
8-other
MSI-H 'medullary type' adenocarcinoma complicating ileal Crohn's disease; further molecular insight into Crohn's-related carcinogenesis.
PMID 18315608·Histopathology·2008
5-case
Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.
PMID 18419787·Clin Endocrinol (Oxf)·2008
4-observational
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
PMID 17397051·Hum Mutat·2007
8-other
Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome.
PMID 17564974·Am J Hum Genet·2007
8-other
VHL mutation analysis in patients with isolated central nervous system haemangioblastoma.
PMID 17264095·Brain·2007
8-other
Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
PMID 17337339·Genomics·2007
8-other
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10.
PMID 17106446·Eur J Hum Genet·2007
8-other
Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.
PMID 17063531·Prenat Diagn·2006
5-case
Upper limb disorders among coopers in the Scotch whisky industry.
PMID 16520360·Occup Med (Lond)·2006
8-other
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
PMID 15999116·Eur J Hum Genet·2005
8-other
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.
PMID 15951966·Fam Cancer·2005
8-other
Solution stability of factor Xa inhibitors as a function of pH.
PMID 15554221·Drug Dev Ind Pharm·2004
4-observational
Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies.
PMID 15564036·Neuromuscul Disord·2004
8-other
Iatrogenic prescribing in acute care: learning from our mistakes.
PMID 15061450·J Gerontol Nurs·2004
5-case
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART).
PMID 12525545·J Med Genet·2003
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
- 8036 MOORSBRIDGE ROAD, SUITE #2
PORTAGE, MI 49024 - Phone
- (269) 327-1438
Quick Facts
- NPI
- 1275645947
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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