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The X chromosome and ovarian functionVIALARD, F; COCQUET, J; CHRISTIN-MAITRE, S et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 218-223, issn 1424-8581, 6 p.Article

Assignment of an anonymous DNA sequence IB/D22 (DXS371) to XP11.1-11.4SPURR, N. K; MITCHELL, C; GOUGH, A. C et al.Disease markers. 1989, Vol 7, Num 4, pp 247-251, issn 0278-0240, 5 p.Article

X chromosome inactivation: theme and variationsMIGEON, B. R.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 8-16, issn 1424-8581, 9 p.Article

ICF syndrome cells as a model system for studying X chromosome inactivationGARTLER, S. M; HANSEN, R. S.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 25-29, issn 1424-8581, 5 p.Article

X chromosomes of American marsupials contain mnimal amounts of ecuchromatinSCHMID, M; FEICHTINGER, W; STEINLEIN, C et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 315-322, issn 1424-8581, 8 p.Article

Reorganization of the X chromosome in voles of the genus MicrotusRUBTSOV, N. B; RUBTSOVA, N. V; ANOPRIYENKO, O. V et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 323-329, issn 1424-8581, 7 p.Article

Integrated kinetics of X chromosome inactivation in differentiating embryonic stem cellsCHAUMEIL, J; OKAMOTO, I; GUGGIARI, M et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 75-84, issn 1424-8581, 10 p.Article

Skewed X inactivation in X-linked disordersVAN DEN VEYVER, Ignatia B.Seminars in reproductive medicine. 2001, Vol 19, Num 2, pp 183-191Article

What causes the abnormal phenotype in a 49,XXXXY male?SARTO, G. E; OTTO, P. G; KUHN, E. M et al.Human genetics. 1987, Vol 76, Num 1, pp 1-4, issn 0340-6717Article

Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X ChromosomeGENDREL, Anne-Valerie; APEDAILE, Anwyn; GIANNOULATOU, Eleni et al.Developmental cell. 2012, Vol 23, Num 2, pp 265-279, issn 1534-5807, 15 p.Article

The role of the X chromosome in mammalian extra embryonic developmentHEMBERGER, M.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 210-217, issn 1424-8581, 8 p.Article

Frequency of tri- and multiradial configurations in fragile X chromosomesSUBRT, I; STIRSKA, K.Human genetics. 1988, Vol 78, Num 2, pp 196-197, issn 0340-6717Article

Refractive errors in the fragile-X syndromeFLOOD, A; SANNER, G.Acta paediatrica scandinavica. 1985, Vol 74, Num 6, issn 0001-656X, 974Article

Inactive X chromosome-specific reduction in placental DNA methylationCOTTON, Allison M; AVILA, Luana; PENAHERRERA, Maria S et al.Human molecular genetics (Print). 2009, Vol 18, Num 19, pp 3544-3552, issn 0964-6906, 9 p.Article

Evolution on the X chromosome : unusual patterns and processesVICOSO, Beatriz; CHARLESWORTH, Brian.Nature reviews. Genetics (Print). 2006, Vol 7, Num 8, pp 645-653, issn 1471-0056, 9 p.Article

X chromosomes, retrogenes and their role in male reproductionWANG, P. Jeremy.Trends in endocrinology and metabolism. 2004, Vol 15, Num 2, pp 79-83, issn 1043-2760, 5 p.Article

X chromosome inactivation, differentiation, and DNA methylation revisited, with a tribute to Susumu OhnoRIGGS, A. D.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 17-24, issn 1424-8581, 8 p.Article

Fertility, sex determination, and the X chromosomeVAIMAN, D.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 224-228, issn 1424-8581, 5 p.Article

Manic-depression locus on X chromosomeVASSART, G; SIMON, P.Lancet (British edition). 1991, Vol 338, Num 8770, issn 0140-6736, p. 821Article

A scaffold for X chromosome inactivationTATTERMUSCH, Anna; BROCKDORFF, Neil.Human genetics. 2011, Vol 130, Num 2, pp 247-253, issn 0340-6717, 7 p.Article

Forensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker setTOMAS, Carmen; SANCHEZ, Juan J; CASTRO, Jose Aurelio et al.Transfusion (Philadelphia, PA). 2010, Vol 50, Num 10, pp 2258-2265, issn 0041-1132, 8 p.Article

X-chromosome inactivation: a hypothesis linking ontogeny and phylogenyHUYNH, Khanh D; LEE, Jeannie T.Nature reviews. Genetics (Print). 2005, Vol 6, Num 5, pp 410-418, issn 1471-0056, 9 p.Article

La cartographie du chromosome X : les localisations connues = Gene mapping of the X chromosomeVERELLEN-DUMOULIN, C.Journal de génétique humaine. 1989, Vol 37, Num 4-5, pp 321-351, issn 0021-7743, 31 p.Article

Effect of folic acid treatment in the fragile X syndromeGUSTAVSON, K.-H; DAHLBOM, K; FLOOD, A et al.Clinical genetics. 1985, Vol 27, Num 5, pp 463-467, issn 0009-9163Article

Mary Lyon and the hypothesis of random X chromosome inactivationHARPER, Peter S.Human genetics. 2011, Vol 130, Num 2, pp 169-174, issn 0340-6717, 6 p.Article

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