Dr. Elizabeth Marie Petty MD
Pediatrician
1500 East Medical Center Dr 3rd Floor Taubman Ct Ann Arbor MI, 48109About
Dr. Elizabeth Petty is a pediatrician practicing in Ann Arbor, MI. Dr. Petty is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Petty diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Petty can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Univ of Wi Med Sch, Madison Wi 1986
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci.
- Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer.
- Support for the availability of prenatal testing for neurological and psychiatric conditions in the psychiatric community.
- Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors.
- Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines.
- Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors.
- Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells.
- Characterisation and genetic mapping of a new X linked deafness syndrome.
- Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas.
- Systemic lupus erythematosus in a man with Noonan syndrome.
- Virtual genome scan: a tool for restriction landmark-based scanning of the human genome.
- Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag.
- Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells.
- Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1.
- Mammalian septins nomenclature.
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