A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
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1. Shaping modern human skull through epigenetic, transcriptional and post-transcriptional regulation of the RUNX2 master bone gene;Scientific Reports;2021-10-29
2. An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation;Frontiers in Genetics;2021-10-19
3. Identification of RUNX2 variants associated with cleidocranial dysplasia;Hereditas;2019-09-16
4. Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family;International Journal of Dentistry;2018-07-04
5. Displasia cleidocraneal: presentación de un caso;Universitas Médica;2016-05-25
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