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IRENE MADRIGAL, PHARMD
PHARMD
Pharmacist
NPI: 1710389200Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PR5514(ME)
Research & Publications (20)
X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.
PMID 18047645·BMC Genomics·2007
4-observational
MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardation.
PMID 17304053·Genet Med·2007
4-observational
Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?
PMID 19531215·BMC Med Genet·2009
4-observational
[Fragile X tremor ataxia syndrome (FXTAS): a new kind of spinocerebelar ataxia associated to fragile X syndrome premutation carriers].
PMID 19473671·Med Clin (Barc)·2009
8-other
Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.
PMID 19367323·Eur J Hum Genet·2009
8-other
Evidence of depressive symptoms in fragile-X syndrome premutated females.
PMID 18628675·Psychiatr Genet·2008
8-other
Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion.
PMID 18412126·Am J Med Genet A·2008
5-case
Screening for FXTAS in 95 Spanish patients negative for Huntington disease.
PMID 18373410·Genet Test·2008
8-other
Trisomy of 19.4 Mb region of chromosome 22 and subtelomeric 17p identified in a male without clinical affectation.
PMID 17853459·Am J Med Genet A·2007
5-case
Complete deletion of ornithine transcarbamylase gene confirmed by CGH array of X chromosome.
PMID 17570074·J Inherit Metab Dis·2007
8-other
Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.
PMID 17431911·Am J Med Genet A·2007
5-case
Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion.
PMID 17431332·Cytogenet Genome Res·2007
5-case
Duplication/deletion mosaicism of the 7q(21.1 --> 31.3) region.
PMID 17163539·Am J Med Genet A·2007
5-case
Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor.
PMID 17099875·Genes Chromosomes Cancer·2007
8-other
Fluorescence in situ hybridization studies using BAC clones of the EVI1 locus in hematological malignancies with 3q rearrangements.
PMID 17011981·Cancer Genet Cytogenet·2006
8-other
Studies of complex Ph translocations in cases with chronic myelogenous leukemia and one with acute lymphoblastic leukemia.
PMID 16616117·Cancer Genet Cytogenet·2006
8-other
A novel mutation in JARID1C gene associated with mental retardation.
PMID 16538222·Eur J Hum Genet·2006
8-other
46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosis.
PMID 15966059·Prenat Diagn·2005
5-case
Coamplified and overexpressed genes at ERBB2 locus in gastric cancer.
PMID 14991576·Int J Cancer·2004
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
- 1012 UNION ST
BANGOR, ME 04401 - Phone
- (207) 404-8100
Quick Facts
- NPI
- 1710389200
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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