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Results 1 - 9 of 9 for Holoprosencephaly 8
  1. ... 6; HPE6 HOLOPROSENCEPHALY 7; HPE7 HOLOPROSENCEPHALY 9; HPE9 HOLOPROSENCEPHALY 8; HPE8 HOLOPROSENCEPHALY 5; HPE5 PubMed Dubourg C, Bendavid C, Pasquier ...
  2. ... mutations cause a significant proportion of autosomal dominant holoprosencephaly. Hum Mol Genet. 1999 Dec;8(13):2479-88. doi: 10.1093/hmg/8. ...
  3. ... Pasquier L, Henry C, Odent S, David V. Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2-8. Citation ... Muenke M, Elledge SJ. Mutations in TGIF cause holoprosencephaly and link NODAL signalling to ... doi: 10.1038/76074. Citation on PubMed Roessler ...
  4. ... Pasquier L, Henry C, Odent S, David V. Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2-8. Citation ... E, Muenke M. Mutations in ZIC2 in human holoprosencephaly: description of a novel ... J Med Genet. 2010 Aug;47(8):513-24. doi: 10.1136/jmg.2009.073049. ...
  5. ... the homeodomain of the human SIX3 gene cause holoprosencephaly. Nat Genet. 1999 Jun;22(2):196-8. doi: 10.1038/9718. Citation on PubMed
  6. ... mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ... 2010 Apr 8. Citation on PubMed White KE, Cabral JM, Davis ...
  7. ... 10.1002/ajmg.a.37869. Epub 2016 Sep 8. No abstract available. Citation on ... association of holoprosencephaly and ectrodactyly. J Med Genet. 2013 Sep;50( ...
  8. ... Health Condition MedlinePlus Genetics provides information about Nonsyndromic holoprosencephaly More About This Health Condition MedlinePlus Genetics provides ...
  9. ... PTCH1 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... cell patterning. The signs and symptoms of nonsyndromic holoprosencephaly are caused by abnormal development of the brain ...