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 81 - 90 of 4,765 for R -"5-DIPHOSPHOMEVALONATE"
  1. Facioscapulohumeral muscular dystrophy 
    ... SL, Frants RR, van der Maarel SM, Tawil R. Clinical features of facioscapulohumeral muscular dystrophy 2. Neurology. ... abstract available. Citation on PubMed Lemmers RJ, Tawil R, Petek LM, Balog J, Block GJ, Santen GW, ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  2. Anonychia congenita 
    ... gene provides instructions for making a protein called R-spondin-4. R-spondin-4 plays a role in the Wnt ... role in the growth and development of nails. R-spondin-4 is active in the skeleton and ...
    https://medlineplus.gov/genetics/condition/anonychia-congenita - Genetics
  3. Senior-Løken syndrome 
    ... 7; SLSN7 PubMed Caridi G, Murer L, Bellantuono R, Sorino P, Caringella DA, Gusmano R, Ghiggeri GM. Renal-retinal syndromes: association of retinal ... Citation on PubMed Otto E, Hoefele J, Ruf R, Mueller AM, Hiller KS, Wolf MT, Schuermann MJ, ...
    https://medlineplus.gov/genetics/condition/senior-loken-syndrome - Genetics
  4. RAD51 gene 
    ... H, Rooimans MA, Oostra AB, Velleuer E, Dietrich R, Bleijerveld OB, Maarten Altelaar AF, Meijers-Heijboer H, ... J, Hood L, Galas D, Wyman C, Balling R, den Dunnen J, de Winter JP, Kanaar R, ...
    https://medlineplus.gov/genetics/gene/rad51 - Genetics
  5. CREBBP gene 
    ... MYELOID; AML NCBI Gene ClinVar Banka S, Sayer R, Breen C, Barton S, Pavaine J, Sheppard SE, ... abstract available. Citation on PubMed Hallam TM, Bourtchouladze R. Rubinstein-Taybi syndrome: molecular findings and therapeutic approaches ...
    https://medlineplus.gov/genetics/gene/crebbp - Genetics
  6. Polymicrogyria 
    ... on PubMed Central Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David ... G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  7. Mucolipidosis type IV 
    ... CR, Quarrell OW, Slaugenhaupt SA, Goldin E, Schiffmann R. The neurogenetics of mucolipidosis type IV. Neurology. 2002 ... Central Misko A, Grishchuk Y, Goldin E, Schiffmann R. Mucolipidosis IV. 2005 Jan 28 [updated 2021 Feb ...
    https://medlineplus.gov/genetics/condition/mucolipidosis-type-iv - Genetics
  8. Koolen-de Vries syndrome 
    ... Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. Seattle (WA): University of Washington, Seattle; 1993- ... Knight SJ, Goldenberg A, Saugier-Veber P, Pfundt R, Vissers LE, Destree A, Grisart B, Rooms L, ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  9. Myoclonic epilepsy with ragged-red fibers 
    ... Lopez-Gallardo E, Jou C, Bujan N, Montero R, Garcia-Cazorla A, Gonzaga D, Ferrer I, Briones P, Ruiz-Pesini E, Pineda M, Artuch R, Montoya J. New mitochondrial DNA mutations in tRNA ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  10. Brugada syndrome 
    ... C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, Gussak I, LeMarec H, Nademanee K, ... 1097(92)90253-j. Citation on PubMed Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
previous · 4 · 5 · 6 · 7 · 8 · 9 · 10 · 11 · 12 · 13 · next