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MARK HANNIBAL, M.D., PH.D.
M.D., PH.D.
Pediatrics Physician
NPI: 1548350432Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
MD00037850(WA)4301099786(MI)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
4301099786(MI)
Research & Publications (20)
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
PMID 19451530·Neurology·2009
8-other
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.
PMID 19139049·Hum Mol Genet·2009
8-other
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study.
PMID 18492087·Clin Genet·2008
5-case
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization.
PMID 18471320·Mol Cytogenet·2008
8-other
Gunshot wounds to the spine: literature review and report on a migratory intrathecal bullet.
PMID 18438477·Am J Orthop (Belle Mead NJ)·2008
5-case
A novel technique of intra-spinous process injection of PMMA to augment the strength of an inter-spinous process device such as the X STOP.
PMID 18277879·Spine (Phila Pa 1976)·2008
8-other
Clinical outcomes in lymphocytopenic lymphatic malformation patients.
PMID 18035935·Lymphat Res Biol·2007
8-other
ProDisc-L total disc replacement: a comparison of 1-level versus 2-level arthroplasty patients with a minimum 2-year follow-up.
PMID 17906573·Spine (Phila Pa 1976)·2007
4-observational
Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
PMID 17886299·Ann Neurol·2007
8-other
Vertebroplasty versus kyphoplasty: biomechanical behavior under repetitive loading conditions.
PMID 16915092·Spine (Phila Pa 1976)·2006
4-observational
Interspinous process decompression with the X-STOP device for lumbar spinal stenosis: a 4-year follow-up study.
PMID 16826002·J Spinal Disord Tech·2006
4-observational
Lymphocytopenia in children with lymphatic malformation.
PMID 16415437·Arch Otolaryngol Head Neck Surg·2006
4-observational
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome.
PMID 16183809·Pediatr Res·2005
4-observational
The monotonic and fatigue properties of osteoporotic thoracic vertebral bodies.
PMID 15770179·Spine (Phila Pa 1976)·2005
8-other
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
PMID 15739154·Am J Hum Genet·2005
8-other
Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum.
PMID 15286162·J Med Genet·2004
5-case
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
PMID 12457340·Am J Hum Genet·2003
4-observational
Upper limb phocomelia associated with increased nuchal translucency in a monochorionic twin pregnancy.
PMID 11883548·J Ultrasound Med·2002
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1500 E MEDICAL CENTER DR, 8TH FLOOR C. S. MOTT CHILDREN'S HOSPITAL
ANN ARBOR, MI 48109 - Phone
- (734) 936-4185
Quick Facts
- NPI
- 1548350432
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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