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Results 1 - 10 of 12 for Confer
  1. 3q29 microdeletion syndrome 
    ... DJ, Pulver AE, Warren ST. Microdeletions of 3q29 confer high risk for schizophrenia. Am J Hum Genet. ... on PubMed Central Mulle JG. The 3q29 deletion confers >40-fold increase in risk for schizophrenia. Mol ...
    https://medlineplus.gov/.../condition/3q29-microdeletion-syndrome - Genetics
  2. Recurrent hydatidiform mole 
    ... MJ, Fisher RA. Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype on digynic triploid ... spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage. J Med ...
    https://medlineplus.gov/.../condition/recurrent-hydatidiform-mole - Genetics
  3. 17q12 deletion syndrome 
    ... 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J ...
    https://medlineplus.gov/genetics/condition/17q12-deletion-syndrome - Genetics
  4. Narcolepsy 
    ... Risch N. Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. ...
    https://medlineplus.gov/genetics/condition/narcolepsy - Genetics
  5. Atelosteogenesis type 3 
    ... substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-3 - Genetics
  6. Larsen syndrome 
    ... substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of ...
    https://medlineplus.gov/genetics/condition/larsen-syndrome - Genetics
  7. Atelosteogenesis type 1 
    ... substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-1 - Genetics
  8. Chordoma 
    ... Parry DM, Kelley MJ. T (brachyury) gene duplication confers major susceptibility to familial chordoma. Nat Genet. 2009 ...
    https://medlineplus.gov/genetics/condition/chordoma - Genetics
  9. IRAK-4 deficiency 
    ... JI, Vogel SN. Distinct mutations in IRAK-4 confer hyporesponsiveness to lipopolysaccharide and interleukin-1 in a ...
    https://medlineplus.gov/genetics/condition/irak-4-deficiency - Genetics
  10. Spondylocarpotarsal synostosis syndrome 
    ... substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of ...
    https://medlineplus.gov/.../spondylocarpotarsal-synostosis-syndrome - Genetics
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