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Results 1 - 5 of 5 for vernon cases
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  1. White-Sutton syndrome 
    ... Wheeler PG, Crain C, Zand D, Weinstein V, Vernon HJ, McClellan R, Krishnamurthy V, Vitazka P, Millan F, Chung WK. De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Cold Spring Harb Mol Case Stud. 2015 Oct;1(1):a000455. doi: 10. ...
    https://medlineplus.gov/genetics/condition/white-sutton-syndrome - Genetics
  2. POGZ gene 
    ... Wheeler PG, Crain C, Zand D, Weinstein V, Vernon HJ, McClellan R, Krishnamurthy V, Vitazka P, Millan F, Chung WK. De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Cold Spring Harb Mol Case Stud. 2015 Oct;1(1):a000455. doi: 10. ...
    https://medlineplus.gov/genetics/gene/pogz - Genetics
  3. Barth syndrome 
    ... PubMed Central Ferreira C, Pierre G, Thompson R, Vernon H. Barth Syndrome. 2014 Oct 9 [updated 2020 ... doi: 10.1097/MOH.0000000000000472. Citation on PubMed Vernon HJ, Sandlers Y, McClellan R, Kelley RI. Clinical ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  4. Thrombocytopenia-absent radius syndrome 
    ... A, Ancliff PJ, Brunner HG, Verschuuren-Bemelmans CC, Vernon E, Brown KW, Newbury-Ecob RA. Thrombocytopenia-absent ... syndrome: a clinical genetic series of 14 further cases. impact of the associated 1q21.1 deletion on ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  5. Meige disease 
    ... Bell R, Brice G, Hasan A, Burnand K, Vernon S, Mansour S, Mortimer P, Jeffery S, Child ...
    https://medlineplus.gov/genetics/condition/meige-disease - Genetics