Dr. David D Weaver M.D.
Geneticist | Clinical Genetics (M.D.)
975 W Walnut St Ib 130 Indianapolis IN, 46202About
Dr. David Weaver practices Genetic Medicine in Indianapolis, IN. As a geneticist, Dr. Weaver 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. Weaver carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Or Hlth Sci Univ Sch of Med, Portland Or 1966
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Cervical spine stenosis and possible vitamin K deficiency embryopathy in an unusual case of chondrodysplasia punctata and an updated classification system.
- Severe lower limb defects in exstrophy of the cloaca.
- Johnson-McMillin syndrome: report of a new case with novel features.
- Adults with VATER association: long-term prognosis.
- Phenotypic spectrum of mosaic trisomy 18: two new patients, a literature review, and counseling issues.
- On the spectrum of limb-body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequence.
- Ramos-Arroyo syndrome: long-term follow-up of previously reported family.
- A report of an apparent new genetic syndrome consisting of joint contractures, keloids, large optic cup-to-disc ratio and renal stones.
- Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a persistent challenge 18 years later.
- Phenotypic variability in trisomy 13 mosaicism: two new patients and literature review.
- A tale of two deletions: a report of two novel 20p13 --> pter deletions.
- Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation family.
- Report of a mother and daughter with the 12q14 microdeletion syndrome.
- Mutations in EZH2 cause Weaver syndrome.
- Severe lateral tibial bowing with short stature in two siblings--a provisionally novel syndrome.
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