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Wallis, D. and Muenke, M. (2000), Mutations in holoprosencephaly. Hum. Mutat., 16: 99-108. https://doi.org/10.1002/1098-1004(200008)16:2<99::AID-HUMU2>3.0.CO;2-0[1]
- Genetic Mutations involved in holoprosencephaly, government sponsored research.
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- ^ Wallis, Deeann; Muenke, Maximilian (2000). "Mutations in holoprosencephaly". Human Mutation. 16 (2): 99–108. doi:10.1002/1098-1004(200008)16:2<99::AID-HUMU2>3.0.CO;2-0. ISSN 1098-1004.
Embryonic Development
In Holoprosencephaly, the neural tube fails to segment, resulting in incomplete separation of the procencephalon at the fifth week of gestation. [1]
Holoprocencephaly
Holoprocencephaly is common birth defect that occurs in 1 of every 8000 live births. [2]
- ^ Winter, Thomas C.; Kennedy, Anne M.; Woodward, Paula J. (2015-01-01). "Holoprosencephaly: A Survey of the Entity, with Embryology and Fetal Imaging". RadioGraphics. 35 (1): 275–290. doi:10.1148/rg.351140040. ISSN 0271-5333.
- ^ Raam, Manu S; Solomon, Benjamin D; Muenke, Maximilian (2011-6). "Holoprosencephaly: A Guide to Diagnosis and Clinical Management". Indian pediatrics. 48 (6): 457–466. ISSN 0019-6061. PMC 4131946. PMID 21743112.
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