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Homozygosity for uromodulin disorders: FJHN and MCKD-type 2REZENDE-LIMA, Wania; PARREIRA, Kleber S; GARCIA-GONZALEZ, Miguel et al.Kidney international. 2004, Vol 66, Num 2, pp 558-563, issn 0085-2538, 6 p.Article

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Gene responsible for Mitochondrial Myopathy and Sideroblastic Anemia (MSA) Maps to chromosome 12q24.33CASAS, Kari; BYKHOVSKAYA, Yelena; MENGESHA, Emebet et al.American journal of medical genetics. 2004, Vol 127A, Num 1, pp 44-49, issn 0148-7299, 6 p.Article

Autosomal Recessive Inheritance of GLUT1 Deficiency SyndromeKLEPPER, J; SCHEFFER, H; ELSAID, M. F et al.Neuropediatrics. 2009, Vol 40, Num 5, pp 207-210, issn 0174-304X, 4 p.Article

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Effects of inbreeding on potential and realized immune responses in Tenebrio molitorRANTALA, Markus J; VIITANIEMI, Heidi; ROFF, Derek A et al.Parasitology (London. Print). 2011, Vol 138, pp 906-912, issn 0031-1820, 7 p., 7Article

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Cohen Syndrome Resulting From a Novel Large Intragenic COH1 Deletion Segregating in an Isolated Greek Island PopulationBUGIANI, Marianna; GYFTODIMOU, Yolanda; KABOHS, Nikolaos et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 17, pp 2221-2226, issn 1552-4825, 6 p.Article

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Discovery of a novel imprinted gene by transcriptional analysis of parthenogenetic embryonic stem cellsSRITANAUDOMCHAI, Hathaitip; HONG MA; CLEPPER, Lisa et al.Human reproduction (Oxford. Print). 2010, Vol 25, Num 8, pp 1927-1941, issn 0268-1161, 15 p.Article

A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing lossYARIZ, K. O; WALSH, T; AKAY, H et al.Clinical genetics. 2012, Vol 81, Num 3, pp 289-293, issn 0009-9163, 5 p.Article

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Novel strategies to minimize progeny inbreeding while maximizing genetic gain using genomic informationPRYCE, J. E; HAYES, B. J; GODDARD, M. E et al.Journal of dairy science. 2012, Vol 95, Num 1, pp 377-388, issn 0022-0302, 12 p.Article