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Results 1 - 10 of 144 for dgs
  1. TBX1 gene 
    ... More About This Health Condition CAFS CTHM DGCR DGS DORV TBX1_HUMAN TBX1C Testis-specific T-box ...
    https://medlineplus.gov/genetics/gene/tbx1 - Genetics
  2. 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
  3. 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
  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. 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
  7. TUBB3 gene 
    ... Pomeroy SL, Crowley WF Jr, Jabs EW, Hunter DG, Grant PE, Engle EC. A novel syndrome caused ... I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, ...
    https://medlineplus.gov/genetics/gene/tubb3 - Genetics
  8. 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
  9. 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
  10. PARK7 gene 
    ... DJ1 NCBI Gene ClinVar Abou-Sleiman PM, Healy DG, Quinn N, Lees AJ, Wood NW. The role ... 10675. Citation on PubMed Abou-Sleiman PM, Healy DG, Wood NW. Causes of Parkinson's disease: genetics ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
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