Carrie Zabel

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Carrie Zabel

Publications by authors named "Carrie Zabel"

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8Publications

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Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.

Am J Hum Genet 2013 Jun 23;92(6):1001-7. Epub 2013 May 23.

Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, NY 10029, USA; Department of Pediatrics, Mount Sinai School of Medicine, New York, NY 10029, USA; Department of Oncological Sciences, Mount Sinai School of Medicine, New York, NY 10029, USA. Electronic address:

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June 2013

Stroke and Stroke-Like Symptoms in Patients with Mutations in the POLG1 Gene.

JIMD Rep 2011 22;1:89-96. Epub 2011 Jun 22.

Mayo Medical School, Mayo Clinic, Rochester, MN, USA.

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February 2013

Improving risk assessment in family medicine through the family history.

J Prim Care Community Health 2010 Oct;1(3):147-51

Department of Family Medicine, Mayo Clinic, Rochester, MN, USA.

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October 2010

Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.

Am J Med Genet A 2008 Apr;146A(7):904-9

Department of Pediatric Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

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April 2008

Bile duct anomalies in a male child with Noonan syndrome: a case for ras and notch pathway synergism.

Am J Med Genet A 2008 Jan;146A(2):261-3

Department of Medical Genetic Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA.

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January 2008

Mitochondrial mutation in a child with distal arthrogryposis.

Am J Med Genet A 2006 Jan;140(2):184-5

Marshfield Clinic, Marshfield, Wisconsin 54449, USA.

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January 2006