المؤلفون: El Alloussi M, Chhoul H, Hariri M, Ramdi H

المصدر: Dentistry. 6

مصطلحات موضوعية: Molar, business.industry, Dentistry, Signs and symptoms, 030206 dentistry, medicine.disease, stomatognathic diseases, 03 medical and health sciences, 0302 clinical medicine, stomatognathic system, Periodontal disease, Hall Technique, medicine, Treatment strategy, Local anesthesia, 030212 general & internal medicine, business, Caries Removal, Early childhood caries

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::396faaebe11660383bbc4e61fa951625
https://doi.org/10.4172/2161-1122.1000385

المؤلفون: Ratbi, I, Falkenberg, KD, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, JE, Chandler, KE, Williams, SJ, Roberts, NA, El Alloussi, M, Black, GC, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S, Cooper, N, Ong, KR, Smith, CEL, Inglehearn, CF, Mighell, AJ, Elcock, C, Poulter, JA, Tischkowitz, M, Davies, SJ, Sefiani, A, Mironov, AA, Newman, WG, Waterham, HR, Van Camp, G

المساهمون: Graduate School, Laboratory for General Clinical Chemistry, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Laboratory Genetic Metabolic Diseases

المصدر: The American journal of human genetics
Ratbi, I, Falkenberg, K D, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, J, Chandler, K E, Williams, S, Roberts, N, El Alloussi, M, Black, G, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S-A, Cooper, N, Ong, K R, Smith, C E L, Inglehearn, C F, Mighell, A J, Elcock, C, Poulter, J A, Tischkowitz, M, Davies, S J, Sefiani, A, Mironov, A, Newman, W, Waterham, H R & Van Camp, G 2015, ' Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. ', American Journal of Human Genetics, vol. 97, no. 4, pp. 535-545 . https://doi.org/10.1016/j.ajhg.2015.08.011
American journal of human genetics, 97(4), 535-545. Cell Press

مصطلحات موضوعية: Adult, Male, Adolescent, Amelogenesis Imperfecta, Hearing Loss, Sensorineural, Nails, Malformed, Article, Young Adult, Genetics, Peroxisomes, Humans, Genetics(clinical), Child, Cells, Cultured, Adenosine Triphosphatases, Infant, Newborn, Infant, Membrane Proteins, Fibroblasts, Prognosis, Pedigree, Survival Rate, Phenotype, Case-Control Studies, Child, Preschool, Mutation, ATPases Associated with Diverse Cellular Activities, Female, Human medicine, Follow-Up Studies

وصف الملف: pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7c7cfdea4a0813b99967b331b96a330c
https://hdl.handle.net/10067/1287660151162165141

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المؤلفون: Ramdi, H., Tahri Jouti, M. A., Lièvremont, M.

المصدر: Biomaterials, Artificial Cells & Immobilization Biotechnology; 1993, Vol. 21 Issue 3, p335-341, 7p

المؤلفون: Tahri Jouti, M. A., Ramdi, H., Lièvremont, M.

المصدر: Biomaterials, Artificial Cells & Immobilization Biotechnology; 1993, Vol. 21 Issue 3, p353-358, 6p

المؤلفون: Jouti, M. A. Tahri, Ramdi, H., Lièvremont, M.

المصدر: Artificial Cells, Blood Substitutes, and Biotechnology; 1993, Vol. 21 Issue: 3 p353-358, 6p

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