Overview
Michael Bober is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Bober and is rated as a Distinguished provider by MediFind in the treatment of Acromesomelic Dysplasia. His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Short Stature (Growth Disorders), Osteotomy, and Myringotomy. Dr. Bober is currently accepting new patients.
His clinical research consists of co-authoring 119 peer reviewed articles and participating in 6 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 4 articles and participated in 1 clinical trial in the study of Acromesomelic Dysplasia.
Insurance
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Accepted insurance plans
- Humana
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
6 Clinical Trials
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Achalasia Microcephaly Syndrome
- Achondroplasia
- Brachydactyly Mononen Type
- Chondrodystrophy
- Meier-Gorlin Syndrome
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Distinguished
- Achondrogenesis
- Acromesomelic Dysplasia
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Chondrodysplasia Punctata Syndrome
- Advanced
- Acromicric Dysplasia
- Genital Dwarfism
- Hypochondroplasia
- Intrauterine Growth Restriction
- Micrognathia
- Mucopolysaccharidoses (MPS)
- Experienced
- Adenoidectomy
- Endoscopy
- Kozlowski Spondylometaphyseal Dysplasia
- Microcephaly Deafness Syndrome
- Multiple Sulfatase Deficiency
- Myringotomy