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Results 1 - 10 of 38 for ln
  1. Lesch-Nyhan syndrome 
    ... syndrome Juvenile hyperuricemia syndrome Lesch-Nyhan disease LND LNS Primary hyperuricemia syndrome Total HPRT deficiency Total hypoxanthine- ... Rare Disorders (NORD) ClinicalTrials.gov LESCH-NYHAN SYNDROME; LNS HYPERURICEMIA, HPRT-RELATED; HRH PubMed Ceballos-Picot I, ...
    https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome - Genetics
  2. GBA gene 
    ... 067. No abstract available. Citation on PubMed Clark LN, Kartsaklis LA, Wolf Gilbert R, Dorado B, Ross ... PubMed or Free article on PubMed Central Clark LN, Ross BM, Wang Y, Mejia-Santana H, Harris ...
    https://medlineplus.gov/genetics/gene/gba - Genetics
  3. Osteoarthritis 
    ... Epub 2012 Nov 22. Citation on PubMed Reynard LN, Loughlin J. The genetics and functional analysis of ... PubMed or Free article on PubMed Central Reynard LN. Analysis of genetics and DNA methylation in osteoarthritis: ...
    https://medlineplus.gov/genetics/condition/osteoarthritis - Genetics
  4. Lesch-Nyhan Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Lesch-Nyhan syndrome (LNS) is a rare, inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT). The lack of ...
    https://www.ninds.nih.gov/.../disorders/lesch-nyhan-syndrome - External Health Links
  5. ABCB11 gene 
    ... abstract available. Citation on PubMed Strautnieks SS, Bull LN, Knisely AS, Kocoshis SA, Dahl N, Arnell H, ... Pawlowska J, Mieli-Vergani G, Knisely AS, Bull LN, Thompson RJ. Severe bile salt export pump deficiency: ...
    https://medlineplus.gov/genetics/gene/abcb11 - Genetics
  6. PGM3-congenital disorder of glycosylation 
    ... PubMed Lundin KE, Hamasy A, Backe PH, Moens LN, Falk-Sorqvist E, Elgstoen KB, Morkrid L, Bjoras ... Gustafsson MO, Lundin KE, Falk-Sorqvist E, Moens LN, Gungor HE, Engelhardt KR, Dziadzio M, Stauss H, ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
  7. PGM3 gene 
    ... PubMed Lundin KE, Hamasy A, Backe PH, Moens LN, Falk-Sorqvist E, Elgstoen KB, Morkrid L, Bjoras ... Gustafsson MO, Lundin KE, Falk-Sorqvist E, Moens LN, Gungor HE, Engelhardt KR, Dziadzio M, Stauss H, ...
    https://medlineplus.gov/genetics/gene/pgm3 - Genetics
  8. 15q13.3 microdeletion 
    ... on PubMed Ziats MN, Goin-Kochel RP, Berry LN, Ali M, Ge J, Guffey D, Rosenfeld JA, ...
    https://medlineplus.gov/genetics/condition/15q133-microdeletion - Genetics
  9. Benign recurrent intrahepatic cholestasis 
    ... AS, Thompson RJ, Freimer NB, Houwen RH, Bull LN. Characterization of mutations in ATP8B1 associated with hereditary ...
    https://medlineplus.gov/...benign-recurrent-intrahepatic-cholestasis - Genetics
  10. CRLF1 gene 
    ... P, Losberger C, Herren S, Gretener D, Menoud LN, Wells TN, Kosco-Vilbois MH, Gauchat JF. Cytokine- ...
    https://medlineplus.gov/genetics/gene/crlf1 - Genetics
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