We found 6 genetics specialists who accept Bronze Choice HSA 6300 - 2 with IVF near Austin, TX.
Dr. Jaya George-Abraham works as a pediatric geneticist in Austin, TX. Dr. George-Abraham's education and training includes medical school at the University of Texas Health Science Center at San Antonio, School of Medicine and residency at a hospital affiliated with the University of Texas Southwestern Medical Center at Dallas. Areas of particular interest for Dr. George-Abraham include genetic counseling. Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and Blue Cross Blue Shield Gold are among the insurance carriers that Dr. George-Abraham accepts. She is professionally affiliated with Seton Healthcare Family. Dr. George-Abraham is accepting new patients.
Clinical interests: Growth Problems, Cognitive Problems, Genetic Counseling, Autism
Dr. Ladonna Immken is an Austin, TX physician who specializes in pediatric genetics. In her practice, Dr. Immken focuses on genetic counseling. She is affiliated with Seton Healthcare Family. Dr. Immken is in-network for Blue Cross/Blue Shield, Coventry, and TRICARE, in addition to other insurance carriers. She has an open panel. Dr. Immken studied medicine at the University of Missouri-Columbia School of Medicine. Her training includes a residency program at Jules Stein Eye Institute.
Clinical interests: Genetic Counseling
Dr. Thomas Hughes sees patients in Austin, TX. His medical specialty is pediatric genetics. He is affiliated with Seton Healthcare Family. Dr. Hughes graduated from the University of Pittsburgh School of Medicine. He is an in-network provider for Aetna EPO, Blue Cross/Blue Shield, and Blue Cross Blue Shield Bronze, in addition to other insurance carriers. Dr. Hughes has received the distinction of Texas Super Doctors.
Dr. James Gibson's specialties are pediatric genetics and clinical biochemical genetics. He practices in Austin, TX. He is an in-network provider for Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and Blue Cross Blue Shield Gold, in addition to other insurance carriers. Before performing his residency at The Children's Hospital of Philadelphia, Dr. Gibson attended Duke University School of Medicine. He is professionally affiliated with Seton Healthcare Family.
Dr. Mathew Putzi works as a molecular genetic pathologist and cytopathologist. Dr. Putzi (or staff) speaks Spanish and Vietnamese. He attended Tufts University School of Medicine and subsequently trained at a hospital affiliated with the University of Michigan for residency. He accepts United Healthcare Compass, United Healthcare Choice, United Healthcare HSA, and more.
Dr. Jose Garcia is a clinical molecular geneticist, general practitioner, and family medicine physician. He attended medical school at Baylor College of Medicine. He accepts United Healthcare Compass, United Healthcare Choice, United Healthcare HSA, and more.
Conditions / Treatments
Medicare Patient Age
Medicare Patient Conditions
Medicare Patient Ethnicity
Medicare Patient Gender
Medicare Patient Insurance Eligibility
Years Since Graduation
- 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.