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Results 1 - 8 of 8 for Holoprosencephaly 5
  1. Nonsyndromic holoprosencephaly 
    ... 7; HPE7 HOLOPROSENCEPHALY 9; HPE9 HOLOPROSENCEPHALY 8; HPE8 HOLOPROSENCEPHALY 5; HPE5 PubMed Dubourg C, Bendavid C, Pasquier L, ... PubMed Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. SIX3 gene 
    ... schizencephaly and further expand the clinical spectrum of holoprosencephaly. Hum Genet. 2010 Mar;127(5):555-61. doi: 10.1007/s00439-010-0797- ... Central Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/gene/six3 - Genetics
  3. Hartsfield syndrome 
    ... de Silva D, Verloes A, Baumann C. Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review. Am J Med Genet A. 2009 Jul;149A(7):1476-81. doi: 10.1002/ajmg.a.32678. Citation on PubMed
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  4. TGIF1 gene 
    ... Central Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  5. ZIC2 gene 
    ... Central Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  6. SHH gene 
    ... Central Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/gene/shh - Genetics
  7. PTCH1 gene 
    ... the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Hum Genet. 2002 Apr;110(4):297-301. doi: 10.1007/s00439-002-0695-5. Epub 2002 Mar 2. Erratum In: Hum Genet ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  8. 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