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Carrie A. Zabel

Observed names: Carrie A Zabel, Carrie Zabel
Institution: Marshfield Clinic
OpenAlex ID: A5080803247
Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis
2013 · John A. Martignetti, Lifeng Tian, et al. · The American Journal of Human Genetics · 205
Sclerocornea associated with the chromosome 22q11.2 deletion syndrome
2008 · Gil Binenbaum, Donna M. McDonald‐McGinn, et al. · American Journal of Medical Genetics Part A · 51
Mitochondrial mutation in a child with distal arthrogryposis
2005 · Elizabeth McPherson, Carrie Zabel · American Journal of Medical Genetics Part A · 17
Stroke and Stroke-Like Symptoms in Patients with Mutations in the POLG1 Gene
2011 · Waleed Brinjikji, Jerry W. Swanson, et al. · JIMD Reports · 10
Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity
2006 · Philip F. Giampietro, Deepti Babu, et al. · American Journal of Medical Genetics Part A · 8
Bile duct anomalies in a male child with Noonan syndrome: A case for ras and notch pathway synergism
2007 · Kristen J. Rasmussen, Ivan Zador, et al. · American Journal of Medical Genetics Part A · 5
Improving Risk Assessment in Family Medicine Through the Family History
2010 · Matthew E. Bernard, Carrie A. Zabel, et al. · Journal of Primary Care & Community Health · 2
Bone Density Studies in Two Patients with Hajdu-Cheney Syndrome
2006 · Jane A. Hocking, Fergus McKiernan, et al. · Journal of Clinical Densitometry · 1
Mayo Clinic office visit. Genetic counseling. An interview with Carrie Zabel, M.S., C.G.C.
2011 · Carrie Zabel · PubMed
Assessing and addressing ongoing information and support needs among individuals with Lynch syndrome
2011 · Anna M Leininger, Mia Resner, et al. · Hereditary Cancer in Clinical Practice
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Works count: 10
Citation count: 299
H-index: 5
I10-index: 4
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