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ALISSA MURCH, M.D.
M.D.
Pediatrics Physician
NPI: 1356570527Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
N1789(TX)56698(WI)
Research & Publications (14)
Classic and desmoplastic medulloblastoma: complete case reports and characterizations of two new cell lines.
PMID 19077040·Neuropathology·2009
5-case
The selective use of rapid aneuploidy screening in prenatal diagnosis.
PMID 19281576·Aust N Z J Obstet Gynaecol·2009
8-other
Overexpression and altered glycosylation of MUC1 in malignant mesothelioma.
PMID 18454162·Br J Cancer·2008
8-other
First trimester predictors of adverse pregnancy outcomes.
PMID 19133038·Aust N Z J Obstet Gynaecol·2008
8-other
A xenograft model of infant leukaemia reveals a complex MLL translocation.
PMID 18218047·Br J Haematol·2008
5-case
Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5.
PMID 17593542·Am J Med Genet A·2007
5-case
First-trimester combined screening for Down syndrome and other fetal anomalies.
PMID 16582125·Obstet Gynecol·2006
4-observational
Primary renal synovial sarcoma confirmed by cytogenetic analysis: a lesion distinct from sarcomatoid renal cell carcinoma.
PMID 15679430·Arch Pathol Lab Med·2005
5-case
Detection of hemizygous deletions in genomic DNA from leukaemia specimens for the diagnosis of patients.
PMID 15607365·Leuk Res·2005
8-other
An investigation into sub-telomeric deletions of chromosome 22 and pervasive developmental disorders.
PMID 14755453·Am J Med Genet B Neuropsychiatr Genet·2004
8-other
Gene expression profiles in a panel of childhood leukemia cell lines mirror critical features of the disease.
PMID 12883040·Mol Cancer Ther·2003
4-observational
Cytogenetic analysis of embryos generated from in vitro matured mouse oocytes reveals an increase in micronuclei due to chromosome fragmentation.
PMID 11958507·J Assist Reprod Genet·2002
7-preclinical
Identification of a novel deletion of the entire OCRL1 gene detected by FISH analysis in a family with Lowe syndrome.
PMID 11149618·Clin Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3501 CRANBERRY BLVD
WESTON, WI 54476 - Phone
- (715) 393-1000
Quick Facts
- NPI
- 1356570527
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 14
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