Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Bollerslev, J.
and
Andersen, P.E.
1988.
Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis.
Bone,
Vol. 9,
Issue. 1,
p.
7.
Bollerslev, Jens
Grøntved, Aksel
and
Anderson, Poul Erik
1988.
Autosomal dominant osteopetrosis: An otoneurological investigation of the two radiological types.
The Laryngoscope,
Vol. 98,
Issue. 4,
p.
411.
Bosley, T. M.
Salih, M. A.
Alorainy, I. A.
Islam, M. Z.
Oystreck, D. T.
Suliman, O. S. M.
Malki, S. a.
Suhaibani, A. H.
Khiari, H.
Beckers, S.
van Wesenbeeck, L.
Perdu, B.
AlDrees, A.
Elmalik, S. A.
Van Hul, W.
and
Abu-Amero, K. K.
2011.
The neurology of carbonic anhydrase type II deficiency syndrome.
Brain,
Vol. 134,
Issue. 12,
p.
3502.
Van Hul, Wim
2012.
Sclerosing bone disorders: a lot of knowns but still some unknowns.
BoneKEy Reports,
Vol. 1,
Issue. 6,
Perdu, Bram
and
Van Hul, Wim
2013.
Genetics of Bone Biology and Skeletal Disease.
p.
361.
Boudin, Eveline
and
Van Hul, Wim
2018.
Sclerosing bone dysplasias.
Best Practice & Research Clinical Endocrinology & Metabolism,
Vol. 32,
Issue. 5,
p.
707.
Boudin, Eveline
and
Van Hul, Wim
2018.
Genetics of Bone Biology and Skeletal Disease.
p.
507.