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Results 1 - 10 of 12 for Holoprosencephaly 1
  1. Nonsyndromic holoprosencephaly 
    ... 3; HPE3 HOLOPROSENCEPHALY 4; HPE4 HOLOPROSENCEPHALY 2; HPE2 HOLOPROSENCEPHALY 1; HPE1 HOLOPROSENCEPHALY 6; HPE6 HOLOPROSENCEPHALY 7; HPE7 HOLOPROSENCEPHALY ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. 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. ... Roessler E, Muenke M. The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236. ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  3. SIX3 gene 
    ... Muenke M, Richieri-Costa A. SIX3 mutations with holoprosencephaly. Am J Med Genet A. 2006 Dec 1;140(23):2577-83. doi: 10.1002/ajmg. ... Roessler E, Muenke M. The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236. ...
    https://medlineplus.gov/genetics/gene/six3 - Genetics
  4. ZIC2 gene 
    ... Roessler E, Muenke M. The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236. ...
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  5. SHH gene 
    ... Roessler E, Muenke M. The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236. ...
    https://medlineplus.gov/genetics/gene/shh - Genetics
  6. Learning about Holoprosencephaly (HPE) From the National Institutes of Health (National Human Genome Research Institute)  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Holoprosencephaly is a disorder caused by the failure of the the embryonic forebrain to ...
    https://www.genome.gov/Genetic-Disorders/Holoprosencephaly - External Health Links
  7. PTCH1 gene 
    ... E, Bale SJ, Muenke M. Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Hum Genet. 2002 Apr;110(4):297-301. ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  8. Hartsfield syndrome 
    Hartsfield syndrome is a rare condition characterized by holoprosencephaly, which is an abnormality of brain development, and ... into two halves, the right and left hemispheres. Holoprosencephaly occurs when the brain fails to divide properly. ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  9. FGFR1 gene 
    ... with Hartsfield syndrome, a rare condition characterized by holoprosencephaly, which is an abnormality of brain development, and ... is unclear how these changes lead specifically to holoprosencephaly and ectrodactyly, the characteristic features of Hartsfield syndrome. ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  10. 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
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