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Results 1 - 10 of 13 for Digenic inheritance
  1. CLCNKB gene 
    ... N, Iijima K, Matsuo M. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics
  2. SLC7A9 gene 
    ... cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotype. J Med Genet. 2005 Jan; ...
    https://medlineplus.gov/genetics/gene/slc7a9 - Genetics
  3. SMCHD1 gene 
    ... Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
  4. DUX4 gene 
    ... Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive ...
    https://medlineplus.gov/genetics/gene/dux4 - Genetics
  5. Facioscapulohumeral muscular dystrophy 
    ... Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  6. CLCNKA gene 
    ... N, Iijima K, Matsuo M. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. J Med ...
    https://medlineplus.gov/genetics/gene/clcnka - Genetics
  7. SLC3A1 gene 
    ... cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotype. J Med Genet. 2005 Jan; ...
    https://medlineplus.gov/genetics/gene/slc3a1 - Genetics
  8. Retinitis pigmentosa 
    ... which are usually distinguished by their pattern of inheritance: autosomal dominant, autosomal recessive, or X-linked.Less ... ZNF513 Retinitis pigmentosa often has an autosomal dominant inheritance pattern, which means one copy of an altered ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  9. Bardet-Biedl syndrome 
    ... PJ, Davidson WS, Beales PL, Lupski JR. Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder. ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  10. PROKR2 gene 
    ... olfactory bulb, a person's sense of smell will be impaired or absent. Misplacement or premature loss ...
    https://medlineplus.gov/genetics/gene/prokr2 - Genetics
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