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Journal of Cellular Biochemistry, ISSN 0730-2312, 08/2007, Volume 101, Issue 6, pp. 1430 - 1438
Journal Article
Motricidade, ISSN 1646-107X, 02/2014, Volume 10, Issue 1, pp. 77 - 87
Este estudo foi realizado com o propósito de desenvolver e validar o sistema de observação da comunicação cinésica do instrutor de fitness, assim como realizar... 
Journal Article
Motricidade, ISSN 1646-107X, 01/2014, Volume 10, Issue 1, p. 77
  The aim of this study was to develop and validate an observational system for the kinesics communication of the fitness instructor, as well as to conduct a... 
Journal Article
Motricidade, ISSN 1646-107X, 01/2014, Volume 10, Issue 1, pp. 77 - 77
The aim of this study was to develop and validate an observational system for the kinesics communication of the fitness instructor, as well as to conduct a... 
Journal Article
ISSN 2045-2322, 05/2014
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have... 
Enfermedades del aparato locomotor | Genètica | Teixit ossi | Malalties de l'aparell locomotor | Genetics | Bones | Bone | Ossos
Journal Article
ISSN 2045-2322, 05/2014
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have... 
Enfermedades del aparato locomotor | Genètica | Teixit ossi | Malalties de l'aparell locomotor | Genetics | Bones | Bone | Ossos
Journal Article
by Reppe, Sjur and Wang, Yunpeng and Thompson, Wesley K and McEvoy, Linda K and Schork, Andrew J and Zuber, Verena and LeBlanc, Marissa and Bettella, Francesco and Mills, Ian G and Desikan, Rahul S and Djurovic, Srdjan and Gautvik, Kaare M and Dale, Anders M and Andreassen, Ole A and Estrada, Karol and Styrkarsdottir, Unnur and Evangelou, Evangelos and Hsu, Yi-Hsiang and Duncan, Emma L and Ntzani, Evangelia E and Oei, Ling and Albagha, Omar M. E and Amin, Najaf and Kemp, John P and Koller, Daniel L and Li, Guo and Liu, Ching-Ti and Minster, Ryan L and Moayyeri, Alireza and Vandenput, Liesbeth and Willner, Dana and Xiao, Su-Mei and Yerges-Armstrong, Laura M and Zheng, Hou-Feng and Alonso, Nerea and Eriksson, Joel and Kammerer, Candace M and Kaptoge, Stephen K and Leo, Paul J and Thorleifsson, Gudmar and Wilson, Scott G and Wilson, James F and Aalto, Ville and Alen, Markku and Aragaki, Aaron K and Aspelund, Thor and Center, Jacqueline R and Dailiana, Zoe and Duggan, David J and Garcia, Melissa and Garcia-Giralt, Natàlia and Giroux, Sylvie and Hallmans, Göran and Hocking, Lynne J and Husted, Lise Bjerre and Jameson, Karen A and Khusainova, Rita and Kim, Ghi Su and Kooperberg, Charles and Koromila, Theodora and Kruk, Marcin and Laaksonen, Marika and Lacroix, Andrea Z and Lee, Seung Hun and Leung, Ping C and Lewis, Joshua R and Masi, Laura and Mencej-Bedrac, Simona and Nguyen, Tuan V and Nogues, Xavier and Patel, Millan S and Prezelj, Janez and Rose, Lynda M and Scollen, Serena and Siggeirsdottir, Kristin and Smith, Albert V and Svensson, Olle and Trompet, Stella and Trummer, Olivia and Van Schoor, Natasja M and Woo, Jean and Zhu, Kun and Balcells, Susana and Brandi, Maria Luisa and Buckley, Brendan M and Cheng, Sulin and Christiansen, Claus and Cooper, Cyrus and Dedoussis, George and Ford, Ian and Frost, Morten and Goltzman, David and González-Macías, Jesús and Kähönen, Mika and Karlsson, Magnus and Khusnutdinova, Elza and Koh, Jung-Min and Kollia, Panagoula and Langdahl, Bente Lomholt and Leslie, William D and ... and GEFOS Consortium
PLoS ONE, ISSN 1932-6203, 12/2015, Volume 10, Issue 12, pp. e0144531 - e0144531
Journal Article
Nature Genetics, ISSN 1061-4036, 1998, Volume 18, Issue 1, pp. 11 - 12
Retinitis pigmentosa (RP) denotes a group of inherited eye disorders characterized by loss of rod photoreceptor function, leading to a progressive degeneration... 
GENETICS & HEREDITY | Homozygote | Frameshift Mutation | ATP-Binding Cassette Transporters - genetics | Macular Degeneration - genetics | Pedigree | Humans | Retinitis Pigmentosa - genetics | Female | Male | Genes, Recessive
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 04/2012, Volume 27, Issue 4, pp. 950 - 953
Journal Article
ISSN 2045-2322, 02/2013
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have... 
Enfermedades del aparato locomotor | Genètica | Teixit ossi | Malalties de l'aparell locomotor | Genetics | Bones | Bone | Ossos
Journal Article
ISSN 2045-2322, 02/2013
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have... 
Enfermedades del aparato locomotor | Genètica | Teixit ossi | Malalties de l'aparell locomotor | Genetics | Bones | Bone | Ossos
Journal Article
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