Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M. G. Butler"'
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
The proximal 15q11–q13 region contains 5 breakpoints (BP1–BP5). The BP1-BP2 region spans approximately 500 kb and contains four evolutionarily conserved genes. The genes in this region are known to play a role in central nervous system developmen
Externí odkaz:
https://doaj.org/article/2da71fecb7aa47cf90187b50812ba998
Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome A follow-up report on 38 cases
Autor:
F J Meaney, M G Butler
Publikováno v:
Clinical Genetics. 28:27-30
Metacarpophalangeal pattern profile (MCPP) was determined on 38 Prader-Willi syndrome individuals and compared with a previous report on 16 patients. Chromosome analysis showed an interstitial deletion of the long arm of chromosome 15 in 20 subjects
Publikováno v:
SIL Proceedings, 1922-2010. 27:3465-3469
Publikováno v:
SIL Proceedings, 1922-2010. 27:273-277
(2000). Utility of species-level identification of Chironomus larvae in biological assessment of prairie lakes. SIL Proceedings, 1922-2010: Vol. 27, No. 1, pp. 273-277.
Publikováno v:
Skeletal Radiology. 25:309-317
A wide variety of masses may be visualized in the posterior knee. Some are encountered incidentally on MRI obtained for seemingly unrelated symptoms; others are palpable and present for MRI characterization. We describe the appearance, significance a
Autor:
P. F. J. Tirman, K. D. Fuchigami, Harry K. Genant, P. Schnarkowski, J. V. Crues, M. G. Butler
Publikováno v:
Radiology. 196:47-50
To determine the magnetic resonance (MR) imaging appearance of meniscal ossicles and correlate that with the radiographic and clinical features.Radiographs and MR images were studied retrospectively in six patients with meniscal ossicles; all patient
Autor:
C. G. Palmer, F. Elder, J. T. Lanman, S. Schwartz, Mark J. Pettenati, M. D. Higgins, Elisabeth A. Keitges, J. Brown, Kathleen W. Rao, F. Grass, R. R. Higgins, M. G. Butler, D. L. Van Dyke, Colleen Jackson-Cook, P. N. Rao, J. L. Smith, P. Cosper, A. J. Carroll, M. C. Phelan, F.W. Luthardt
Publikováno v:
American Journal of Medical Genetics. 55:171-187
We present a large review of 446 cases of paracentric inversions (PAI), including 120 new cases, to assess their incidence, distribution, inheritance, modes of ascertainment, interchromosomal effects, viable recombinant offspring, and clinical releva
Publikováno v:
Archiv für Hydrobiologie. 128:423-436
Autor:
M. G. Butler
Publikováno v:
Archives of dermatology and syphilology. 55(4)
THE OBSERVATIONS and conclusions concerning the bizarre syndrome atypical lichen planus tropicalis are based on the study of this disease in a group of 247 cases. The patients were cared for at a debarkation hospital for evacuees by air from the Paci
Publikováno v:
British Journal of Ophthalmology. 76:486-490
In situ hybridisation and immunohistochemical studies were conducted on six surgically excised subretinal membranes of proliferative vitreoretinopathy to investigate whether displacement of retinal pigment epithelial and glial cells to subretinal mem