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1. The registry of the German Network for Systemic Scleroderma: frequency of disease subsets and patterns of organ involvement.

URL:
http://mediatum.ub.tum.de/node?id=736875
http://mediatum.ub.tum.de/doc/736875/document.pdf  

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2. Dental Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545689
http://www.ncbi.nlm.nih.gov/pubmed/23160629  
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3. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)


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4. Two novel large ANKH deletion mutations in sporadic cases with craniometaphyseal dysplasia

URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417334
http://www.ncbi.nlm.nih.gov/pubmed/22150416  
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5. Oculofaciocardiodental (OFCD) Syndrome: a Rare Case and Review of the Literature

URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354011
http://www.ncbi.nlm.nih.gov/pubmed/21740180  
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6. Introduction of a Phe377del Mutation in ANK Creates a Mouse Model for Craniometaphyseal Dysplasia

URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697624
http://www.ncbi.nlm.nih.gov/pubmed/19257826  
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7. Induced Pluripotent Stem Cell Reprogramming by Integration-Free Sendai Virus Vectors from Peripheral Blood of Patients with Craniometaphyseal Dysplasia

URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC
http://www.ncbi.nlm.nih.gov/pubmed/24219578  
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8. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)

URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033186
http://www.ncbi.nlm.nih.gov/pubmed/21149338  
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9. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)


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10. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD)


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