Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 56 for dgs
  1. Nephrogenic diabetes insipidus 
    ... INSIPIDUS, NEPHROGENIC, 1, X-LINKED; NDI1 PubMed Bichet DG. Nephrogenic diabetes insipidus. Adv Chronic Kidney Dis. 2006 ... 01.006. Citation on PubMed Fujiwara TM, Bichet DG. Molecular biology of hereditary diabetes insipidus. J Am ...
    https://medlineplus.gov/.../condition/nephrogenic-diabetes-insipidus - Genetics
  2. Primary myelofibrosis 
    ... DC, Avezov E, Li J, Kollmann K, Kent DG, Aziz A, Godfrey AL, Hinton J, Martincorena I, ... JJ, Lee SJ, Golub TR, Wadleigh M, Gilliland DG, Levine RL. MPLW515L is a novel somatic activating ...
    https://medlineplus.gov/genetics/condition/primary-myelofibrosis - Genetics
  3. Congenital fibrosis of the extraocular muscles 
    ... Citation on PubMed Heidary G, Engle EC, Hunter DG. Congenital fibrosis of the extraocular muscles. Semin Ophthalmol. ... I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  4. Gorlin syndrome 
    ... hmg/10.7.757. Citation on PubMed Evans DG, Howard E, Giblin C, Clancy T, Spencer H, ... 1002/ajmg.a.33139. Citation on PubMed Evans DG. Nevoid Basal Cell Carcinoma Syndrome. 2002 Jun 20 [ ...
    https://medlineplus.gov/genetics/condition/gorlin-syndrome - Genetics
  5. Neurofibromatosis type 2 
    ... PubMed or Free article on PubMed Central Evans DG, Howard E, Giblin C, Clancy T, Spencer H, ... 1002/ajmg.a.33139. Citation on PubMed Evans DG. Neurofibromatosis type 2 (NF2): a clinical and molecular ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2 - Genetics
  6. X-linked infantile nystagmus 
    ... OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara ... M, Taylor K, Leroy BP, Moore AT, Hunter DG, Hertle RW, Tarpey P, Langmann A, Lindner S, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  7. Retinitis pigmentosa 
    ... Central Daiger SP, Sullivan LS, Gire AI, Birch DG, Heckenlively JR, Bowne SJ. Mutations in known genes ... Citation on PubMed Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Lewis RA, Garcia ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  8. Essential thrombocythemia 
    ... DC, Avezov E, Li J, Kollmann K, Kent DG, Aziz A, Godfrey AL, Hinton J, Martincorena I, ... R, Bernard O, Delhommeau F, Vainchenker W, Gilliland DG, Levine RL. TET2 mutations and their clinical correlates ...
    https://medlineplus.gov/genetics/condition/essential-thrombocythemia - Genetics
  9. Facioscapulohumeral muscular dystrophy 
    ... GN, Bakker B, Bamshad MJ, Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of an ... Straasheijm KR, van Ommen GJ, Padberg GW, Miller DG, Tapscott SJ, Tawil R, Frants RR, van der ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  10. Schwannomatosis 
    ... A, McCann E, Trump D, Prescott T, Evans DG. Molecular characterisation of SMARCB1 and NF2 in familial ... on PubMed Central MacCollin M, Chiocca EA, Evans DG, Friedman JM, Horvitz R, Jaramillo D, Lev M, ...
    https://medlineplus.gov/genetics/condition/schwannomatosis - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · next