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Results 1 - 6 of 6 for Holoprosencephaly 6
  1. ... 4; HPE4 HOLOPROSENCEPHALY 2; HPE2 HOLOPROSENCEPHALY 1; HPE1 HOLOPROSENCEPHALY 6; HPE6 HOLOPROSENCEPHALY 7; HPE7 HOLOPROSENCEPHALY 9; HPE9 HOLOPROSENCEPHALY ...
  2. ... M. Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. J Med Genet. 2009 Jun;46(6):389-98. doi: 10.1136/jmg.2008.063818. ...
  3. ... Sommer A, Wieczorek D, Brown SA, Muenke M. Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination. Hum Mol Genet. 2001 Apr 1;10(8):791-6. doi: 10.1093/hmg/10.8.791. Citation ...
  4. ... 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 ...
  5. ... S A. 2006 Apr 18;103(16):6281-6. doi: 10.1073/pnas.0600962103. Epub 2006 Apr ... association of holoprosencephaly and ectrodactyly. J Med Genet. 2013 Sep;50( ...
  6. ... Health Condition MedlinePlus Genetics provides information about Nonsyndromic holoprosencephaly More About This Health Condition MedlinePlus Genetics provides ...