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Hypophosphatasia.
Mornet E
Orphanet J Rare Dis 2007, 2:40
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BioMed Central articles that cite the above article:

1.


Research article    
Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles
Fauvert D, Brun-Heath I, Lia-Baldini AS, Bellazi L, Taillandier A, Serre JL, de Mazancourt P, Mornet E
BMC Medical Genetics 2009, 10:51 (6 June 2009)
 [Abstract] [Full text] [PDF] [PubMed] [Related articles]
2.


Research    
Orodental phenotype and genotype findings in all subtypes of hypophosphatasia
Reibel A, Manière MC, Clauss F, Droz D, Alembik Y, Mornet E, Bloch-Zupan A
Orphanet Journal of Rare Diseases 2009, 4:6 (21 February 2009)
 [Abstract] [Full Text] [PDF] [PubMed] [Related articles]
3.


Research article    
Prosthetic rehabilitation of hypophosphatasia: a case report
Bai B, Baltaciolu E, Aydoan E, Tamam E
Cases Journal 2009, 2:7626 (12 December 2008)
 [Abstract] [Full Text] [PDF]

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