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Results 1 - 10 of 75 for Rp -cAMPS
  1. Retinitis pigmentosa 
    ... other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing Registry: Retinitis pigmentosa Cone ... for Rare Disorders (NORD) ClinicalTrials.gov RETINITIS PIGMENTOSA; RP PubMed Daiger SP, Bowne SJ, Sullivan LS. Perspective ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  2. Liddle syndrome 
    ... Y, Canessa C, Iwasaki T, Rossier B, Lifton RP. Hypertension caused by a truncated epithelial sodium channel ... Shimkets R, Nelson-Williams C, Rossier BC, Lifton RP. A de novo missense mutation of the beta ...
    https://medlineplus.gov/genetics/condition/liddle-syndrome - Genetics
  3. Aldosterone-producing adenoma 
    ... G, Akerstrom G, Wang W, Carling T, Lifton RP. K+ channel mutations in adrenal aldosterone-producing adenomas ... P, Carling T, Fahlke C, Hidalgo P, Lifton RP. Somatic and germline CACNA1D calcium channel mutations in ...
    https://medlineplus.gov/.../condition/aldosterone-producing-adenoma - Genetics
  4. Pseudohypoaldosteronism type 2 
    ... HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP. Mutations in kelch-like 3 and cullin 3 ... H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP. Human hypertension caused by mutations in WNK kinases. ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
  5. Nearsightedness 
    ... Myopia; Burdon KP, Craig JE, Iyengar SK, Igo RP Jr, Lass JH Jr; Fuchs' Genetics Multi-Center ... Biino G, Concas MP, Schwantes-An TH, Igo RP Jr, Cuellar-Partida G, Martin NG, Craig JE, ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  6. X-linked infantile nystagmus 
    ... S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, ... M, Kumar AS, Farooq SJ, Degg C, Gale RP, Reinecke RD, Woodruff G, Langmann A, Lindner S, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  7. 7q11.23 duplication syndrome 
    ... LA, Miller DT, Raffalli P, Harris DJ, Erickson RP, Cunniff C, Clark GD, Blazo MA, Peiffer DA, ... RM, Curland M, Grice DE, Gunel M, Lifton RP, Mane SM, Martin DM, Shaw CA, Sheldon M, ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  8. Erythrokeratodermia variabilis et progressiva 
    ... R, Loring EC, Morel KD, Lauren CT, Lifton RP, Bilguvar K, Paller AS, Choate KA. Dominant De ... AW, Diaz LA, Goldsmith LA, Paller AS, Lifton RP, Baserga SJ, Choate KA. Mutations in KDSR Cause ...
    https://medlineplus.gov/...hrokeratodermia-variabilis-et-progressiva - Genetics
  9. Usher syndrome 
    ... caused by an eye disease called retinitis pigmentosa (RP), which affects the layer of light-sensitive tissue ... C, Garcia-Garcia G, Rodrigo R, Vazquez-Manrique RP, Blanco-Kelly F, Ayuso C, Roux AF, Jaijo ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  10. Lymphedema-distichiasis syndrome 
    ... PubMed or Free article on PubMed Central Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, ... on PubMed Central Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, ...
    https://medlineplus.gov/.../lymphedema-distichiasis-syndrome - Genetics
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