about
Rare causes of scoliosis and spine deformity: experience and particular featuresRegulation of postnatal bone homeostasis by TGFβTissue-specific calibration of extracellular matrix material properties by transforming growth factor-β and Runx2 in bone is required for hearingA novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.Dysregulation of chondrogenesis in human cleidocranial dysplasiaCharacterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.Cleidocranial dysplasia.Odontomas and supernumerary teeth: is there a common origin?A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia.Molecular genetics of supernumerary tooth formation.Cone-beam computed tomography: An inevitable investigation in cleidocranial dysplasia.A rare presentation of cleidocranial dysplasia.Manifestation and treatment in a cleidocranial dysplasia patient with a RUNX2 (T420I) mutation.Cleidocranial dysplasia: a rare cause of disproportionate severe short statureType X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.Cleidocranial dysplasia with hearing loss.Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.A Runx2 threshold for the cleidocranial dysplasia phenotypeCharacterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.Multiple impacted teeth: report of 3 cases.Hunches on hunchbacks.Cranioplasty Using a Modified Split Calvarial Graft Technique in Cleidocranial Dysplasia.Histological examination and clinical evaluation of the jawbone of an adult patient with cleidocranial dysplasia: a case report.Cleidocranial dysplasia (CCD) causing respiratory distress syndrome in a newborn infant. A case report.Orthodontic treatment of a patient with cleidocranial dysplasia: A case report.A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia.Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient.Abnormal differentiation of dental pulp cells in cleidocranial dysplasia.Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.The management of ADHD and associated problems in a young person with cleidocranial dysostosis (CCD) and mild intellectual disability.De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.Oro-dental features of Pallister-Killian syndrome: Evaluation of 21 European probands.Hypogonadotropic hypogonadism associated with cleidocranial dysostosis.Cleidocranial Dysplasia-dental Disorder Treatment and Audiology Diagnosis.Pure de novo partial trisomy 6p in a girl with craniosynostosisAnesthetic management during a cesarean section in a patient with cleidocranial dysplasia: a case report
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
A natural history of cleidocranial dysplasia.
@en
A natural history of cleidocranial dysplasia.
@nl
type
label
A natural history of cleidocranial dysplasia.
@en
A natural history of cleidocranial dysplasia.
@nl
prefLabel
A natural history of cleidocranial dysplasia.
@en
A natural history of cleidocranial dysplasia.
@nl
P2093
P2860
P356
P1476
A natural history of cleidocranial dysplasia.
@en
P2093
P2860
P356
10.1002/AJMG.10024
P577
2001-11-01T00:00:00Z