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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

Regions of homozygosity and their impact on complex diseases and traitsCHEE SENG KU; NAIDOO, Nasheen; SHU MEI TEO et al.Human genetics. 2011, Vol 129, Num 1, pp 1-15, issn 0340-6717, 15 p.Article

A homozygous mutation in LTBP2 causes isolated microspherophakiaKUMAR, Arun; DUVVARI, Maheswara R; PRABHAKARAN, Venkatesh C et al.Human genetics. 2010, Vol 128, Num 4, pp 365-371, issn 0340-6717, 7 p.Article

A powerful score test to detect positive selection in genome-wide scansMING ZHONG; LANGE, Kenneth; PAPP, Jeanette C et al.European journal of human genetics. 2010, Vol 18, Num 10, pp 1148-1159, issn 1018-4813, 12 p.Article

Assessment of homozygosity levels in the mito-gynogenetic torafugu (Takifugu rubripes) by genome-wide SNP analysesHONG ZHANG; HIROSE, Yusuke; WATABE, Shugo et al.Aquaculture (Amsterdam). 2013, Vol 380-383, pp 114-119, issn 0044-8486, 6 p.Article

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

Mutation of CANT1 Causes Desbuquois DysplasiaFADEN, Maha; AL-ZAHRANI, Fatema; ARAFAH, Dia et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 5, pp 1157-1160, issn 1552-4825, 4 p.Article

Clinical and genetic heterogeneity in Desbuquois dysplasiaFAIVRE, Laurence; LE MERRER, Martine; ZERRES, Klaus et al.American journal of medical genetics. 2004, Vol 128A, Num 1, pp 29-32, issn 0148-7299, 4 p.Article

Significance of H63D homozygosity in a Basque population with hemochroniatosisCASTIELLA, Agustin; ZAPTA, Eva; DE JUAN, Maria Dolores et al.Journal of gastroenterology and hepatology. 2010, Vol 25, Num 7, pp 1295-1298, issn 0815-9319, 4 p.Article

Morphogenetic variability during selection of elite water polo playersCVJETICANIN, Suzana; MARINKOVIC, Dragoslav.Journal of sports sciences (Print). 2009, Vol 27, Num 9, pp 941-947, issn 0264-0414, 7 p.Article

An Autoinflammatory Disease Due to Homozygous Deletion of the IL1RN LocusREDDY, Sreelatha; SHUANGJIA; GEOFFREY, Rhonda et al.The New England journal of medicine. 2009, Vol 360, Num 23, pp 2438-2444, issn 0028-4793, 7 p.Article

Genomic Patterns of Homozygosity in Worldwide Human PopulationsPEMBERTON, Trevor J; ABSHER, Devin; FELDMAN, Marcus W et al.American journal of human genetics. 2012, Vol 91, Num 2, pp 275-292, issn 0002-9297, 18 p.Article

Extended tracts of homozygosity in outbred human populationsGIBSON, Jane; MORTON, Newton E; COLLINS, Andrew et al.Human molecular genetics (Print). 2006, Vol 15, Num 5, pp 789-795, issn 0964-6906, 7 p.Article

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephalyGUVEN, Ayse; GUNDUZ, Aysegul; BOZOGLU, Tarik M et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 189-194, issn 1364-6745, 6 p.Article

Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/CSHEN, J. J; BROWN, C. A; LUPSKI, J. R et al.Journal of medical genetics. 2003, Vol 40, Num 11, pp 854-857, issn 0022-2593, 4 p.Article

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALSBLAIN, C. R. V; BRUNTON, S; WILLIAMS, S. C. R et al.Journal of neurology, neurosurgery and psychiatry. 2011, Vol 82, Num 8, pp 843-849, issn 0022-3050, 7 p.Article

Runs of Homozygosity in European PopulationsMCQUILLAN, Ruth; LEUTENEGGER, Anne-Louise; MACLEOD, Andrew K et al.American journal of human genetics. 2008, Vol 83, Num 3, pp 359-372, issn 0002-9297, 14 p.Article

Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansionHORSNELL, Katherine; ALI, Manir; MALIK, Saghira et al.European journal of medical genetics. 2006, Vol 49, Num 5, pp 396-401, issn 1769-7212, 6 p.Article

The first characterization of homozygous HOX gene mutation in humansCOBURN, B.Clinical genetics. 2006, Vol 69, Num 3, pp 205-206, issn 0009-9163, 2 p.Article

Persistent NKH with transient or absent symptoms and a homozygous GLDC mutationKORMAN, Stanley H; BONEH, Avihu; ICHINOHE, Akiko et al.Annals of neurology. 2004, Vol 56, Num 1, pp 139-143, issn 0364-5134, 5 p.Article

Homozygous deletion of HFE produces a phenotype similar to the HFE p.C282Y/p.C282Y genotypeLE GAC, Gérald; GOURLAOUEN, Isabelle; RONSIN, Christophe et al.Blood. 2008, Vol 112, Num 13, pp 5238-5240, issn 0006-4971, 3 p.Article

Haplotype homozygosity and derived alleles in the human genomeFRY, Andrew E; TRAFFORD, Clare J; KIMBER, Martin A et al.American journal of human genetics. 2006, Vol 78, Num 6, pp 1053-1059, issn 0002-9297, 7 p.Article

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association datasetHERON, Elizabeth A; CORMICAN, Paul; DONOHOE, Gary et al.Schizophrenia research. 2014, Vol 154, Num 1-3, pp 79-82, issn 0920-9964, 4 p.Article

Young-Onset Parkinsonism due to Homozygous Duplication of α-Synuclein in a Consanguineous FamilyKOJOVIC, Maja; SHEERIN, Una-Marie; BHATIA, Kailash P et al.Movement disorders. 2012, Vol 27, Num 14, pp 1827-1829, issn 0885-3185, 3 p.Article

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutationsHAGENAH, J. M; BECKER, B; BRÜGGEMANN, N et al.Journal of neurology, neurosurgery and psychiatry. 2008, Vol 79, Num 9, pp 1077-1080, issn 0022-3050, 4 p.Article

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