Ozcelik T., Akarsu N., Uz E., Caglayan S., Gulsuner S., Onat OE., Tan M., Tan U. Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.. „Proceedings of the National Academy of Sciences of the United States of America”. 11 (105), s. 4232–6, marzec 2008. DOI: 10.1073/pnas.0710010105. PMID: 18326629.
Malinger G., Lev D., Lerman-Sagie T. The fetal cerebellum. Pitfalls in diagnosis and management.. „Prenatal diagnosis”. 4 (29), s. 372–80, kwiecień 2009. DOI: 10.1002/pd.2196. PMID: 19194867.
Boltshauser E. Cerebellar hypoplasias.. „Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn”, s. 115–27, 2007. DOI: 10.1016/S0072-9752(07)87008-4. PMID: 18809022.
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Ozcelik T., Akarsu N., Uz E., Caglayan S., Gulsuner S., Onat OE., Tan M., Tan U. Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.. „Proceedings of the National Academy of Sciences of the United States of America”. 11 (105), s. 4232–6, marzec 2008. DOI: 10.1073/pnas.0710010105. PMID: 18326629.
Philip N., Chabrol B., Lossi AM., Cardoso C., Guerrini R., Dobyns WB., Raybaud C., Villard L. Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia.. „Journal of medical genetics”. 6 (40), s. 441–6, czerwiec 2003. PMID: 12807966.
S.S.BalciS.S. i inni, Cervical diastematomyelia in cervico-oculo-acoustic (Wildervanck) syndrome: MRI findings, „Clinical dysmorphology”, 11 (2), 2002, s. 125-128, PMID: 12002143.
Malinger G., Lev D., Lerman-Sagie T. The fetal cerebellum. Pitfalls in diagnosis and management.. „Prenatal diagnosis”. 4 (29), s. 372–80, kwiecień 2009. DOI: 10.1002/pd.2196. PMID: 19194867.
Boltshauser E. Cerebellar hypoplasias.. „Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn”, s. 115–27, 2007. DOI: 10.1016/S0072-9752(07)87008-4. PMID: 18809022.
