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Results 1 - 5 of 5 for Holoprosencephaly 7
  1. SHH gene 
    ... The morphogen signaling network in forebrain development and holoprosencephaly. J Neuropathol Exp Neurol. 2007 Jul;66(7):566-75. doi: 10.1097/nen.0b013e3180986e1b. Citation ...
    https://medlineplus.gov/genetics/gene/shh - Genetics
  2. PTCH1 gene 
    ... 9. More About This Health Condition At least seven mutations in the PTCH1 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  3. TGIF1 gene 
    ... Functional analysis of mutations in TGIF associated with holoprosencephaly. Mol Genet Metab. 2007 Jan;90(1):97-111. doi: 10.1016/j.ymgme.2006.07.011. Epub 2006 Sep 7. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  4. FGFR1 gene 
    ... have an abnormality in their brain development called holoprosencephaly. They also have a malformation of the hands ... is unclear how these changes lead specifically to holoprosencephaly and split hand/foot in people with Hartsfield ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  5. FGF8 gene 
    ... Health Condition MedlinePlus Genetics provides information about Nonsyndromic holoprosencephaly More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/fgf8 - Genetics