Advanced in CHST3-Related Skeletal Dysplasia

Dr. Michael B. Bober

Medical Genetics
A.i. Dupont Hospital For Children, 1600 Rockland Road, 
Wilmington, DE 
Clinical Trials:Currently Recruiting for 3 Trials
Accepting New Patients

Advanced in CHST3-Related Skeletal Dysplasia
A.i. Dupont Hospital For Children, 1600 Rockland Road, 
Wilmington, DE 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Michael Bober is a Medical Genetics provider in Wilmington, Delaware. Dr. Bober is rated as an Advanced provider by MediFind in the treatment of CHST3-Related Skeletal Dysplasia. His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is currently accepting new patients.

His clinical research consists of co-authoring 124 peer reviewed articles and participating in 6 clinical trials. MediFind looks at clinical research from the past 15 years.

Specialties
Medical Genetics
Licenses
Clinical Genetics in DE
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Health Care Services Corporation
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • OTHER COMMERCIAL
  • OTHER MEDICARE
  • OTHER MEDICARE PART D
  • PPO
Highmark
  • EPO
  • HMO
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Independent Health
  • EPO
  • POS
  • PPO
Wellcare
  • EPO
  • HMO
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • MEDICARE-MEDICAID PLAN
  • OTHER MEDICARE
  • OTHER MEDICARE PART D

Locations

A.i. Dupont Hospital For Children, 1600 Rockland Road, Wilmington, DE 19803
Call: 302-651-4000

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

Primordial Dwarfism Registry at Nemours Children's Hospital, Delaware
Primordial Dwarfism Registry at Nemours Children's Hospital, Delaware
Enrollment Status: Recruiting
Publish Date: October 01, 2025
Rare Diseases Clinical Research Network Brittle Bone Disease Consortium Longitudinal Study of Osteogenesis Imperfecta
Rare Diseases Clinical Research Network Brittle Bone Disease Consortium Longitudinal Study of Osteogenesis Imperfecta
Enrollment Status: Recruiting
Publish Date: August 13, 2025
Rhizomelic Chondrodysplasia Punctata Registry at Nemours Children's Health
Rhizomelic Chondrodysplasia Punctata Registry at Nemours Children's Health
Enrollment Status: Recruiting
Publish Date: July 11, 2025
Phase 2, Open-Label, Dose-Escalation and Dose-Expansion Study of Infigratinib, an FGFR 1-3-Selective Tyrosine Kinase Inhibitor, in Children With Achondroplasia: PROPEL 2
Phase 2, Open-Label, Dose-Escalation and Dose-Expansion Study of Infigratinib, an FGFR 1-3-Selective Tyrosine Kinase Inhibitor, in Children With Achondroplasia: PROPEL 2
Enrollment Status: Completed
Publish Date: October 22, 2025
Intervention Type: Drug
Study Drug: Infigratinib
Study Phase: Phase 2
Prospective Clinical Assessment Study in Children With Achondroplasia: The PROPEL Trial
Prospective Clinical Assessment Study in Children With Achondroplasia: The PROPEL Trial
Enrollment Status: Active_not_recruiting
Publish Date: April 11, 2025
A Multicenter, Multinational, Observational Morquio A Registry Study (MARS)
A Multicenter, Multinational, Observational Morquio A Registry Study (MARS)
Enrollment Status: Completed
Publish Date: March 05, 2024
Intervention Type: Drug
View 3 Less Clinical Trials

122 Total Publications

Long-term outcomes of elosulfase alfa enzyme replacement therapy in adults with MPS IVA: a sub-analysis of the Morquio A Registry Study (MARS).
Long-term outcomes of elosulfase alfa enzyme replacement therapy in adults with MPS IVA: a sub-analysis of the Morquio A Registry Study (MARS).
Journal: Orphanet journal of rare diseases
Published: April 30, 2025
View All 122 Publications
Similar Doctors
Advanced in CHST3-Related Skeletal Dysplasia
Dr. Mahim Jain
Medical Genetics | Pediatrics
Advanced in CHST3-Related Skeletal Dysplasia
Dr. Mahim Jain
Medical Genetics | Pediatrics
1600 Rockland Rd, 
Wilmington, DE 
 (1.6 miles away)
302-651-4200
Languages Spoken:
English
See accepted insurances
Accepting New Patients

Mahim Jain is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Jain is rated as a Distinguished provider by MediFind in the treatment of CHST3-Related Skeletal Dysplasia. His top areas of expertise are Osteogenesis Imperfecta, Spondyloepimetaphyseal Dysplasia Strudwick Type, Miller-Dieker Syndrome, and Lissencephaly 1. Dr. Jain is currently accepting new patients.

Experienced in CHST3-Related Skeletal Dysplasia
Dr. Dena R. Matalon
Medical Genetics | Pediatrics
Experienced in CHST3-Related Skeletal Dysplasia
Dr. Dena R. Matalon
Medical Genetics | Pediatrics
3401 Civic Center Blvd, 9nw63, 
Philadelphia, PA 
 (21.1 miles away)
215-590-1220
Languages Spoken:
English
See accepted insurances

Dena Matalon is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Matalon is rated as a Distinguished provider by MediFind in the treatment of CHST3-Related Skeletal Dysplasia. Her top areas of expertise are Campomelia Cumming Type, Microcephaly Deafness Syndrome, Coffin-Lowry Syndrome, and Nevoid Basal Cell Carcinoma Syndrome.

VIEW MORE CHST3-RELATED SKELETAL DYSPLASIA DOCTORS

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as 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.

Learn more about MediFind’s expert tiers

Find Dr. Bober's expertise for a condition
ConditionClose
  • Elite
  • Achalasia Microcephaly Syndrome
    Dr. Bober is
    Elite
    . Learn about Achalasia Microcephaly Syndrome.
    See more Achalasia Microcephaly Syndrome experts
  • Achondrogenesis
    Dr. Bober is
    Elite
    . Learn about Achondrogenesis.
    See more Achondrogenesis experts
  • Achondroplasia
    Dr. Bober is
    Elite
    . Learn about Achondroplasia.
    See more Achondroplasia experts
  • Acromesomelic Dysplasia
    Dr. Bober is
    Elite
    . Learn about Acromesomelic Dysplasia.
    See more Acromesomelic Dysplasia experts
  • Acromesomelic Dysplasia Campailla Martinelli Type
    Dr. Bober is
    Elite
    . Learn about Acromesomelic Dysplasia Campailla Martinelli Type.
    See more Acromesomelic Dysplasia Campailla Martinelli Type experts
  • Acromesomelic Dysplasia Hunter Thompson Type
    Dr. Bober is
    Elite
    . Learn about Acromesomelic Dysplasia Hunter Thompson Type.
    See more Acromesomelic Dysplasia Hunter Thompson Type experts
View All 21 Elite Conditions
  • Distinguished
  • Acromicric Dysplasia
    Dr. Bober is
    Distinguished
    . Learn about Acromicric Dysplasia.
    See more Acromicric Dysplasia experts
  • Chondrodysplasia Punctata Syndrome
    Dr. Bober is
    Distinguished
    . Learn about Chondrodysplasia Punctata Syndrome.
    See more Chondrodysplasia Punctata Syndrome experts
  • Cortical Dysplasia
    Dr. Bober is
    Distinguished
    . Learn about Cortical Dysplasia.
    See more Cortical Dysplasia experts
  • Diastrophic Dysplasia
    Dr. Bober is
    Distinguished
    . Learn about Diastrophic Dysplasia.
    See more Diastrophic Dysplasia experts
  • Kozlowski Spondylometaphyseal Dysplasia
    Dr. Bober is
    Distinguished
    . Learn about Kozlowski Spondylometaphyseal Dysplasia.
    See more Kozlowski Spondylometaphyseal Dysplasia experts
  • Micrognathia
    Dr. Bober is
    Distinguished
    . Learn about Micrognathia.
    See more Micrognathia experts
View All 12 Distinguished Conditions
  • Advanced
  • Atelosteogenesis Type 2
    Dr. Bober is
    Advanced
    . Learn about Atelosteogenesis Type 2.
    See more Atelosteogenesis Type 2 experts
  • Buschke-Ollendorff Syndrome
    Dr. Bober is
    Advanced
    . Learn about Buschke-Ollendorff Syndrome.
    See more Buschke-Ollendorff Syndrome experts
  • Cartilage-Hair Hypoplasia
    Dr. Bober is
    Advanced
    . Learn about Cartilage-Hair Hypoplasia.
    See more Cartilage-Hair Hypoplasia experts
  • Chondrodysplasia, Grebe Type
    Dr. Bober is
    Advanced
    . Learn about Chondrodysplasia, Grebe Type.
    See more Chondrodysplasia, Grebe Type experts
  • CHST3-Related Skeletal Dysplasia
    Dr. Bober is
    Advanced
    . Learn about CHST3-Related Skeletal Dysplasia.
    See more CHST3-Related Skeletal Dysplasia experts
  • Craniometaphyseal Dysplasia
    Dr. Bober is
    Advanced
    . Learn about Craniometaphyseal Dysplasia.
    See more Craniometaphyseal Dysplasia experts
View All 36 Advanced Conditions
  • Experienced
  • 2q37 Deletion Syndrome
    Dr. Bober is
    Experienced
    . Learn about 2q37 Deletion Syndrome.
    See more 2q37 Deletion Syndrome experts
  • 3M Syndrome
    Dr. Bober is
    Experienced
    . Learn about 3M Syndrome.
    See more 3M Syndrome experts
  • 3MC Syndrome
    Dr. Bober is
    Experienced
    . Learn about 3MC Syndrome.
    See more 3MC Syndrome experts
  • 47 XYY Syndrome
    Dr. Bober is
    Experienced
    . Learn about 47 XYY Syndrome.
    See more 47 XYY Syndrome experts
  • Aase Syndrome
    Dr. Bober is
    Experienced
    . Learn about Aase Syndrome.
    See more Aase Syndrome experts
  • Abruzzo-Erickson Syndrome
    Dr. Bober is
    Experienced
    . Learn about Abruzzo-Erickson Syndrome.
    See more Abruzzo-Erickson Syndrome experts
View All 99 Experienced Conditions
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