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Results 1 - 10 of 198 for crs
  1. Caudal regression syndrome 
    ... dysgenesis syndrome Caudal dysplasia sequence Caudal regression sequence CRS Lumbo-sacral agenesis SA/CRS Sacral agenesis Sacral defect with anterior meningocele Genetic ...
    https://medlineplus.gov/.../condition/caudal-regression-syndrome - Genetics
  2. Familial glucocorticoid deficiency 
    ... 6736(93)90208-x. Citation on PubMed Hughes CR, Chung TT, Habeb AM, Kelestimur F, Clark AJ, ... Epub 2010 Apr 28. Citation on PubMed Hughes CR, Guasti L, Meimaridou E, Chuang CH, Schimenti JC, ...
    https://medlineplus.gov/.../familial-glucocorticoid-deficiency - Genetics
  3. Glutaric acidemia type I 
    ... B, Burgard P, Dixon M, Fleissner S, Greenberg CR, Harting I, Hoffmann GF, Karall D, Koeller DM, ... F, Athayde L, Manfredini V, Wajner M, Vargas CR. Oxidative damage in glutaric aciduria type I patients ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  4. GCDH gene 
    ... DE, Schlesinger S, Christensen E, Schwartz M, Greenberg CR, Elpeleg ON. Glutaryl-CoA dehydrogenase mutations in glutaric ... 0.CO;2-K. Citation on PubMed Greenberg CR, Prasad AN, Dilling LA, Thompson JR, Haworth JC, ...
    https://medlineplus.gov/genetics/gene/gcdh - Genetics
  5. ACAD8 gene 
    ... N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J. Identification of isobutyryl-CoA ... AM, Young SP, Koeberl DD, Millington DS, Roe CR, Roe DS, Wanders RJ, Ruiter JP, Keppen LD, ...
    https://medlineplus.gov/genetics/gene/acad8 - Genetics
  6. Bowen-Conradi syndrome 
    ... J, Cattini PA, Koetter P, Wrogemann K, Greenberg CR, Entian KD, Zelinski T, Triggs-Raine B. Mutation ... D, Innes AM, Lemire EG, Lowry RB, Greenberg CR, Triggs-Raine BL, Morgan K, Wrogemann K, Fujiwara ...
    https://medlineplus.gov/genetics/condition/bowen-conradi-syndrome - Genetics
  7. Warfarin resistance 
    ... Free article on PubMed Central Oldenburg J, Muller CR, Rost S, Watzka M, Bevans CG. Comparative genetics ... K, Seifried E, Scharrer I, Tuddenham EG, Muller CR, Strom TM, Oldenburg J. Mutations in VKORC1 cause ...
    https://medlineplus.gov/genetics/condition/warfarin-resistance - Genetics
  8. Isobutyryl-CoA dehydrogenase deficiency 
    ... N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J. Identification of isobutyryl-CoA ... AM, Young SP, Koeberl DD, Millington DS, Roe CR, Roe DS, Wanders RJ, Ruiter JP, Keppen LD, ...
    https://medlineplus.gov/.../isobutyryl-coa-dehydrogenase-deficiency - Genetics
  9. Nonketotic hyperglycinemia 
    ... 31030. No abstract available. Citation on PubMed Coughlin CR 2nd, Swanson MA, Kronquist K, Acquaviva C, Hutchin ... NV, Fenton LZ, Levek C, Tong S, Coughlin CR 2nd, Hennermann JB, Wortmann SB, Van Hove JLK. ...
    https://medlineplus.gov/.../condition/nonketotic-hyperglycinemia - Genetics
  10. Progressive familial heart block 
    ... H, Fukuhara S, Watanabe H, Shimizu W, Bezzina CR, Hasdemir C, Mugishima H, Makiyama T, Baruteau A, ... Koopmann TT, Le Scouarnec S, Yang T, Ingram CR, Schott JJ, Demolombe S, Probst V, Anselme F, ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
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