Septo-optic dysplasia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Septo-optic dysplasia" in English language version.

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9nih.gov

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5doi.org

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3semanticscholar.org

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archive.org

Gleason, CA; Devascar, S (5 October 2011). "Congenital malformations of the Central Nervous System". Avery's Diseases of the Newborn (9 ed.). Saunders. p. 857. ISBN 978-1437701340.

doi.org

Webb EA, Dattani MT (April 2010). "Septo-optic dysplasia". European Journal of Human Genetics. 18 (4): 393–7. doi:10.1038/ejhg.2009.125. PMC 2987262. PMID 19623216.
Ganau M, Huet S, Syrmos N, Meloni M, Jayamohan J (2019). "Neuro-Ophthalmological Manifestations Of Septo-Optic Dysplasia: Current Perspectives". Eye and Brain. 11 (11): 37–47. doi:10.2147/EB.S186307. PMC 6805786. PMID 31695544.
Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Mårtensson IL, et al. (June 1998). "Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse". Nature Genetics. 19 (2): 125–33. doi:10.1038/477. PMID 9620767. S2CID 28880292.
Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, Braz P, et al. (September 2018). "Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study". European Journal of Medical Genetics. 61 (9): 483–488. doi:10.1016/j.ejmg.2018.05.010. PMID 29753093. S2CID 21673637.
Borchert M (March 2012). "Reappraisal of the optic nerve hypoplasia syndrome". Journal of Neuro-Ophthalmology. 32 (1): 58–67. doi:10.1097/WNO.0b013e31824442b8. PMID 22330852. S2CID 12131899.

nih.gov

pubmed.ncbi.nlm.nih.gov

Webb EA, Dattani MT (April 2010). "Septo-optic dysplasia". European Journal of Human Genetics. 18 (4): 393–7. doi:10.1038/ejhg.2009.125. PMC 2987262. PMID 19623216.
Ganau M, Huet S, Syrmos N, Meloni M, Jayamohan J (2019). "Neuro-Ophthalmological Manifestations Of Septo-Optic Dysplasia: Current Perspectives". Eye and Brain. 11 (11): 37–47. doi:10.2147/EB.S186307. PMC 6805786. PMID 31695544.
Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Mårtensson IL, et al. (June 1998). "Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse". Nature Genetics. 19 (2): 125–33. doi:10.1038/477. PMID 9620767. S2CID 28880292.
Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, Braz P, et al. (September 2018). "Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study". European Journal of Medical Genetics. 61 (9): 483–488. doi:10.1016/j.ejmg.2018.05.010. PMID 29753093. S2CID 21673637.
Borchert M (March 2012). "Reappraisal of the optic nerve hypoplasia syndrome". Journal of Neuro-Ophthalmology. 32 (1): 58–67. doi:10.1097/WNO.0b013e31824442b8. PMID 22330852. S2CID 12131899.

ncbi.nlm.nih.gov

Webb EA, Dattani MT (April 2010). "Septo-optic dysplasia". European Journal of Human Genetics. 18 (4): 393–7. doi:10.1038/ejhg.2009.125. PMC 2987262. PMID 19623216.
Ganau M, Huet S, Syrmos N, Meloni M, Jayamohan J (2019). "Neuro-Ophthalmological Manifestations Of Septo-Optic Dysplasia: Current Perspectives". Eye and Brain. 11 (11): 37–47. doi:10.2147/EB.S186307. PMC 6805786. PMID 31695544.

rarediseases.info.nih.gov

"Septo-Optic Dysplasia Spectrum". Genetic and Rare Diseases Information Center (GARD). Retrieved 5 August 2021.

ghr.nlm.nih.gov

"Septo-Optic Dysplasia". Genetics Home Reference. U.S. National Library of Medicine. Retrieved 16 July 2015.

ox.ac.uk

ora.ox.ac.uk

Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, Braz P, et al. (September 2018). "Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study". European Journal of Medical Genetics. 61 (9): 483–488. doi:10.1016/j.ejmg.2018.05.010. PMID 29753093. S2CID 21673637.

semanticscholar.org

api.semanticscholar.org

Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Mårtensson IL, et al. (June 1998). "Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse". Nature Genetics. 19 (2): 125–33. doi:10.1038/477. PMID 9620767. S2CID 28880292.
Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, Braz P, et al. (September 2018). "Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study". European Journal of Medical Genetics. 61 (9): 483–488. doi:10.1016/j.ejmg.2018.05.010. PMID 29753093. S2CID 21673637.
Borchert M (March 2012). "Reappraisal of the optic nerve hypoplasia syndrome". Journal of Neuro-Ophthalmology. 32 (1): 58–67. doi:10.1097/WNO.0b013e31824442b8. PMID 22330852. S2CID 12131899.

telegraph.co.uk

Singh A (25 January 2021). "Katie Price's dilemma over what's best for disabled son will be familiar to many". The Telegraph.

whonamedit.com

synd/2548 at Who Named It?

worldcat.org

search.worldcat.org

Daroff RB, Jankovic J, Mazziotta JC, Pomeroy SL (2015-10-25). Bradley's neurology in clinical practice (Seventh ed.). London. ISBN 9780323339162. OCLC 932031625.{{cite book}}: CS1 maint: location missing publisher (link)