-
1دورية أكاديمية
المؤلفون: Large, J. F.Aff1, Aff3, Hasmun, N., Lawson, J. A., Elcock, C., Vettore, M. V., Rodd, H. D.
المصدر: European Archives of Paediatric Dentistry. 21(2):185-191
-
2
المؤلفون: Hasmun, N., Vettore, M.V., Lawson, J.A., Elcock, C., Zaitoun, H., Rodd, H.D.
مصطلحات موضوعية: stomatognathic diseases
وصف الملف: application/pdf
-
3دورية أكاديمية
المؤلفون: Rawlinson, A., Elcock, C., Cheung, A., Al-Buhairi, A., Khanna, S., Walsh, T.F., Ellwood, R.P.
المصدر: In Journal of Dentistry 2005 33(9):781-788
-
4دورية أكاديمية
المؤلفون: Khalaf, K., Robinson, D.L., Elcock, C., Smith, R.N. *, Brook, A.H.
المصدر: In Archives of Oral Biology 2005 50(2):243-248
-
5
المؤلفون: Shore, R. C., Bäckman, B., Elcock, C., Brook, A. H., Brookes, S. J., Kirkham, J.
المصدر: Cells Tissues Organs. 191(4):301-306
مصطلحات موضوعية: Enamel, Amelogenesis imperfecta, Local hypoplastic, ENAM, Enamelin
وصف الملف: print
-
6
المؤلفون: Smith, RN, Elcock, C, Abdellatif, A, Bäckman, Birgitta, Russell, JM, Brook, AH
المصدر: Archives of Oral Biology. 54(Suppl 1):S86-S92
مصطلحات موضوعية: Amelogenesis Imperfecta, Enamel defects, Image analysis, EDI
وصف الملف: print
-
7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8
المؤلفون: Elcock, C, Smith, RN, Bäckman, Birgitta, Brook, AH, Simpson, J
المصدر: European Journal of Oral Science. 114(suppl 1):365-369
مصطلحات موضوعية: ODONTOLOGY, ODONTOLOGI
وصف الملف: print
-
9
المؤلفون: Elcock, C, Smith, RN, Abdellatif, A, Bäckman, B, Brook, AH, Simpson, J
المصدر: European Journal of Oral Science. 114(suppl 1):35-38
مصطلحات موضوعية: ODONTOLOGY, ODONTOLOGI
وصف الملف: print
-
10Heimler syndrome is caused by hypomorphic mutations in the peroxisome-biogenesis genes PEX1 and PEX6
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 Pressمصطلحات 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