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 Cohen,  
 

Holoprosencephaly: Clinical, anatomic, and molecular dimensions.

Holoprosencephaly is addressed under the following headings: alobar, semilobar, and lobar holoprosencephaly; arrhinencephaly; agenesis of the corpus callosum; pituitary abnormalities; hindbrain abnormalities; syntelencephaly; aprosencephaly/atelencephaly; neural tube defects; facial anomalies; median cleft lip; minor facial anomalies; single maxillary central incisor; holoprosencephaly-like phenotype; epidemiology; genetic causes of holoprosencephaly; teratogenic causes of holoprosencephaly; SHH mutations; ZIC2 mutations; SIX3 mutations; TGIF mutations; PTCH mutations; GLI2 mutations; FAST1 mutations; TDGF1 mutations; and DHCR7 mutations. Birth Defects Research (Part A) 76:658-673, 2006. (c) 2006 Wiley-Liss, Inc.[1]

References

  1. Holoprosencephaly: Clinical, anatomic, and molecular dimensions. Cohen, M.M. Birth Defects Res. Part A Clin. Mol. Teratol. (2006) [Pubmed]
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