Dr. Laurie Heron Seaver M.D.
Geneticist | Clinical Genetics (M.D.)
25 MICHIGAN ST NE GRAND RAPIDS MI, 49503About
Dr. Laurie Seaver practices Genetic Medicine in Honolulu, HI. As a geneticist, Dr. Seaver performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Seaver carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Spondylocarpotarsal synostosis syndrome and cervical instability.
- Decline in prevalence of neural tube defects in a high-risk region of the United States.
- Adverse environmental exposures in pregnancy: teratology in adolescent medicine practice.
- Neural tube defects and associated anomalies in South Carolina.
- Birth defects research: improving surveillance methods and addressing epidemiologic questions and public health issues.
- New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
- ACMG practice guideline: genetic evaluation of short stature.
- A neonatal death due to medium-chain acyl-CoA dehydrogenase deficiency: utilization of the neonatal metabolic screen in a functional approach to sudden unexplained infant death.
- Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome.
- Monozygotic twins discordant for trisomy 13.
- Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation.
- The perinatal presentation of cardiofaciocutaneous syndrome.
- Aortic aneurysm in three siblings with multiple congenital contractures.
- Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defects.
- Mosaic tetrasomy 20p associated with osteoporosis and recurrent fractures.
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