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Publications by B. Vonderstrass

Mutation Analysis of Core Binding Factor A1 in Patients With Cleidocranial Dysplasia

American Journal of Human Genetics

English

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Parietal Foramina With Cleidocranial Dysplasia Is Caused by Mutation in MSX2

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CBCT Findings in Cleidocranial Dysplasia

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Survival Is Poorer in Patients With Secondary Core Binding Factor Acute Myelogenous Leukemia Compared With De Novo Core Binding Factor Leukemia.

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Cleidocranial Dysplasia Accompanied With Pseudohypoparathyroidism I: Case Report.

Japanese Journal of Oral & Maxillofacial Surgery

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Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph

Cardiovascular Medicine

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Gene-Expression Analysis Identifies IGFBP2 Dysregulation in Dental Pulp Cells From Human Cleidocranial Dysplasia

Frontiers in Genetics

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Population-Based Disparities in Survival Among Patients With Core-Binding Factor Acute Myeloid Leukemia: A SEER Database Analysis

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Structural and Functional Characterization of Runx1 Point Mutations Identified in Leukemia and Cleidocranial Dysplasia Patients.

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A 13-Year-Old Caucasian Boy With Cleidocranial Dysplasia: A Case Report

BMC Research Notes

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