Discover open access scientific publications

Search, annotate, share and cite publications

Publications by I. Quack

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

American Journal of Human Genetics

English

Related publications

Parietal Foramina With Cleidocranial Dysplasia Is Caused by Mutation in MSX2

European Journal of Human Genetics

English

CBCT Findings in Cleidocranial Dysplasia

Scholars Journal of Dental Sciences

English

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

English

Cleidocranial Dysplasia Accompanied With Pseudohypoparathyroidism I: Case Report.

Japanese Journal of Oral & Maxillofacial Surgery

English

Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph

Cardiovascular Medicine

English

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

Frontiers in Genetics

Molecular Medicine

English

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

Leukemia Research

Cancer Research

English

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

English

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

BMC Research Notes

Molecular Biology

English