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21“…Features recent advances and new applications in graph edge coloring Reviewing recent advances in the Edge Coloring Problem, Graph Edge Coloring: Vizing's Theorem and Goldberg's Conjecture provides an overview of the current state of the science, explaining the interconnections among the results obtained from important graph theory studies. …”
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22por Beeby, MorganEnlace del recurso
Publicado 2019
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23“…Goldberg's GHQ was translated into Hindi. An emphasis was made to have the language of common use. …”
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26“…Braneworld scenarios with compact extra-dimensions need the volume of the extra space to be stabilized. Goldberger and Wise have introduced a simple mechanism, based on the presence of a bulk scalar field, able to stabilize the radius of the Randall-Sundrum model. …”
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27Psychometric Properties of The Goldberg Anxiety and Depression Scale (GADS) In Ecuadorian Population“…The objective of the present study was to analyze the psychometric properties of validity and reliability of the Goldberg Anxiety and Depression Scale (GADS) in Ecuadorian university students, since a cultural validation of the instrument has not been found in Ecuador. …”
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28por MacKenzie, Katherine C., de Graaf, Bianca M., Syrimis, Andreas, Zhao, Yuying, Brosens, Erwin, Mancini, Grazia M. S., Schot, Rachel, Halley, Dicky, Wilke, Martina, Vøllo, Arve, Flinter, Frances, Green, Andrew, Mansour, Sahar, Pilch, Jacek, Stark, Zornitza, Zamba‐Papanicolaou, Eleni, Christophidou‐Anastasiadou, Violetta, Hofstra, Robert M. W., Jongbloed, Jan D. H., Nicolaou, Nayia, Tanteles, George A., Brooks, Alice S., Alves, Maria M.“…Goldberg–Shprintzen syndrome (GOSHS) is caused by loss of function variants in the kinesin binding protein gene (KIFBP). …”
Publicado 2020
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29por SALEHPOUR, Shadab, HASHEMI-GORJI, Feyzollah, SOLTANI, Ziba, GHAFOURI-FARD, Soudeh, MIRYOUNESI, Mohammad“…Goldberg-Shprintzen syndrome (OMIM 609460) (GOSHS) is an autosomal recessive multiple congenital anomaly syndrome distinguished by intellectual disability, microcephaly, and dysmorphic facial characteristics. …”
Publicado 2017
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30por Frank, John W.Enlace del recurso
Publicado 2022
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33“…The authors have calculated the correction to the Goldberger-Treiman relation for the /sup 3/H-/sup 3/He transition due to the deuteron- nucleon break-up mechanism. …”
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34por Huxley, Peter, Krayer, Anne, Poole, Rob, Gromadzka, Alicja, Jie, Daniel Lai, Nafees, Sadia“…The first description of this ‘pathway’ to care and its levels and filters was published by Goldberg and Huxley in 1980. AIMS: To conduct a review of papers relevant to the application of the Goldberg–Huxley model in the 21st century. …”
Publicado 2023
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35por Doyle, Alexander J., Doyle, Jefferson J., Bessling, Seneca L., Maragh, Samantha, Lindsay, Mark E., Schepers, Dorien, Gillis, Elisabeth, Mortier, Geert, Homfray, Tessa, Sauls, Kimberly, Norris, Russell A., Huso, Nicholas D., Leahy, Dan, Mohr, David W., Caulfield, Mark J., Scott, Alan F., Destrée, Anne, Hennekam, Raoul C., Arn, Pamela H., Curry, Cynthia J., Van Laer, Lut, McCallion, Andrew S., Loeys, Bart L., Dietz, Harry C.“…Taken together, these data have engendered controversy regarding the specific role of TGF-β in disease pathogenesis. Shprintzen-Goldberg syndrome (SGS) has considerable phenotypic overlap with MFS and LDS, including aortic aneurysm(6-8). …”
Publicado 2012
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36“…Autosomal recessive mutations in KIAA1279 cause a rare neurological disorder, Goldberg-Shprintzen syndrome (GOSHS), characterized by microcephaly, polymicrogyria, intellectual disability, axonal neuropathy, thin corpus callosum and peripheral neuropathy. …”
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38por Choi, Jamie H., Li, Rachel, Gannaway, Rachel, Causey, Tahnee N., Harrison, Anna, Couser, Natario L.“…Shprintzen–Goldberg craniosynostosis syndrome (SGS) is a rare autosomal dominant condition that was first documented in literature in 1982. …”
Publicado 2020
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39“…The level of radiographic bony union (Goldberg method) was assessed by three orthopedic surgeons. …”
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