Physician

Medical Genetics

Gary Gottesman practices Medical Genetics. He graduated from University of Michigan Medical School. Gary S. Gottesman is a published physician. He has 20 publications published. The most current publication "X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature."

Publications

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• Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.
• PHEX 3'-UTR c.*231A > G Near The Polyadenylation Signal Is A Relatively Common, Mild, American Mutation That Masquerades As Sporadic Or X-Linked Recessive Hypophosphat...
• Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy.
• Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.
• Mystery solved: The evolution of diagnostic abilities in genetic testing.
• Newborn screening tests in the 21st century: what PAs need to know.
• The genetics encounter: different from the typical clinic visit.
• Enhancement of drug delivery to bone: characterization of human tissue-nonspecific alkaline phosphatase tagged with an acidic oligopeptide.
• Epimerase-deficiency galactosemia is not a binary condition.
• The challenges of medical genetics and the primary care practitioner.
• Marrow cell transplantation for infantile hypophosphatasia.
• Hypertrophic cardiomyopathy in a newborn infant.
• Clinic-based study of plexiform neurofibromas in neurofibromatosis 1.
• International Morquio A Registry: clinical manifestation and natural course of Morquio A disease.
• Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864.
• A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.
• Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting.
• X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature.
• Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin.

Schools

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• University of Mi Med Sch

• St Louis Childrens Hospital

Doctors Specialties

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• Clinical Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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• Blue Cross Blue Shield
• Great West Healthcare-Cigna PPO
• MedHealthInsurance
• Medicare MCR
• Molina
• MultiPlan PPO
• PHCS Network PPO

Education

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• University of Michigan Medical School

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