We found 4 genetics specialists who accept MultiPlan near Saint Louis, MO.
Dr. Marcia Willing's area of specialization is pediatric genetics. She is in-network for several insurance carriers, including Anthem, Blue Cross/Blue Shield, and Coventry. After attending Virginia Commonwealth University (VCU) School of Medicine, Dr. Willing completed her residency training at Cincinnati Children's Hospital Medical Center. Her hospital/clinic affiliations include Barnes-Jewish West County Hospital, Washington University Physicians, and St. Louis Children's Hospital.
Clinical interests: Metabolic Disorders, Genetic Counseling, Marfan Syndrome, Birth Defects
Dr. Diana Gray works as a genetics specialist, obstetrician, and gynecologist in Saint Louis, MO. She attended medical school at the University of Illinois College of Medicine at Chicago. Her medical residency was performed at Washington University Medical Center in St. Louis. In Dr. Gray's practice, she is particularly interested in prenatal diagnosis and ultrasound (sonogram). She takes Anthem, Blue Cross/Blue Shield, Coventry, and more. Dr. Gray is professionally affiliated with Missouri Baptist Medical Center, Washington University Physicians, and Barnes-Jewish Hospital.
Clinical interests: Prenatal Ultrasound, Down Syndrome, Ultrasound, Pregnancy, Genetic Counseling, Prenatal Diagnosis, ... (Read more)
Dr. Dorothy Grange sees patients in Saint Louis, MO. Her medical specialty is pediatric genetics. She takes Anthem, Blue Cross/Blue Shield, Coventry, and more. Dr. Grange studied medicine at the University of Florida College of Medicine. She completed her residency training at a hospital affiliated with the University of Florida Health Science Center and a hospital affiliated with the University of Wisconsin. Her hospital/clinic affiliations include Washington University Physicians, St. Louis Children's Hospital, and Barnes-Jewish Hospital.
Clinical interests: Metabolic Disorders, Chromosomal Disorders, Genetic Counseling, Marfan Syndrome, Birth Defects, ... (Read more)
Dr. James Crane practices genetics. Dr. Crane is especially interested in ultrasound (sonogram). He is affiliated with Washington University Physicians and Barnes-Jewish Hospital. He attended medical school at Indiana University School of Medicine. His residency was performed at Barnes-Jewish Hospital. Anthem, Blue Cross/Blue Shield, and Coventry are among the insurance carriers that Dr. Crane accepts. Dr. Crane is not currently accepting new patients.
Clinical interests: Prenatal Ultrasound, Down Syndrome, Ultrasound, Prenatal Diagnosis, Birth Defects
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- Single gene disorders, the result of a single mutated gene. Examples include Huntington’s disease, which causes jerky movements, and sickle-cell anemia, where red blood cells have an abnormal, rigid shape.
- Inborn metabolic disorders, which are a specific type of single gene disorder that results in abnormalities in the way the body chemically processes proteins, carbohydrates or fats. Some examples are Urea Cycle Disorder (where ammonia builds up in the body) and Gaucher’s Disease (where fatty substances build up in cells and organs).
- Chromosomal disorders, where gene-carrying chromosomes do not pair up correctly or are missing. Some examples are Klinefelter Syndrome, a sex-chromosome disorder, and Down Syndrome.
- Congenital abnormalities (commonly known as birth defects), which can be caused by genetic abnormalities. They also can happen because of illness or environmental exposure during pregnancy (such as with rubella), or for unknown reasons.
- Other common diseases that have hereditary traits, such diabetes, autism, and some types of cancer.
- Clinical Genetics: This overarching branch of medical genetics deals with the treatment and management of hereditary diseases.
- Biomechanical Genetics: This branch deals with metabolic disorders, such as galactosemia and phenylketonuria.
- Cytogenetics: This specialty deals with chromosomes and their associated diseases, as well as testing their structure and number.
- Molecular Genetics: This specialty focuses on DNA, interpreting DNA sequencing and other tests, and relating DNA information to specific diseases.