Log on / register
Feedback | Support | My details
Hypophosphatasia.
Mornet E
Orphanet J Rare Dis 2007, 2:40
[Full text] [PubMed] [Related articles] [Cited on BioMed Central]


printer friendly 
to  [Help]

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]

You can also check ISI Web of Science for additional citations (subscription required)
printer friendly 
to  [Help]
Terms and Conditions Privacy statement Information for advertisers Jobs at BMC Contact us
© 1999-2009 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.