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Results 1 to 25 of 5014

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Coordination of the random asynchronous replication of autosomal lociSINGH, Nandita; EBRAHIMI, Farah A. W; GIMELBRANT, Alexander A et al.Nature genetics. 2003, Vol 33, Num 3, pp 339-341, issn 1061-4036, 3 p.Article

Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal dataWOODING, Stephen; OSTLER, Christopher; RAVI PRASAD, B. V et al.Human genetics. 2004, Vol 115, Num 3, pp 221-229, issn 0340-6717, 9 p.Article

MID-PACHYTENE CHROMOMERE MAPS OF HUMAN AUTOSOMESJHANWAR SC; BURNS JP; ALONSO ML et al.1982; CYTOGENETICS AND CELL GENETICS; ISSN 0301-0171; CHE; DA. 1982; VOL. 33; NO 3; PP. 240-248; BIBL. 2 P.Article

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article

Selection at a diallelic autosomal locus in a dioecious populationSZUCS, J. M.Journal of mathematical biology (Print). 1991, Vol 29, Num 8, pp 693-713, issn 0303-6812Article

The size of prometaphase chromosome segments: tables using percentages of haploid autosome length (750 band stage)DANIEL, A.Clinical genetics. 1985, Vol 28, Num 3, pp 216-224, issn 0009-9163Article

SCREENING FOR AUTOSOMAL ABERRATIONS.HIGURASHI M; SEGAWA M; MATSUI I et al.1977; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1977; VOL. 66; NO 4; PP. 501-504; BIBL. 10 REF.Article

Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuriaCALADO, Joaquim; SOTO, Karina; CLEMENTE, Carla et al.Human genetics. 2004, Vol 114, Num 3, pp 314-316, issn 0340-6717, 3 p.Article

An X-to-autosome retrogene is required for spermatogenesis in miceBRADLEY, Julie; BALTUS, Andrew; SKALETSKY, Helen et al.Nature genetics. 2004, Vol 36, Num 8, pp 872-876, issn 1061-4036, 5 p.Article

Investigation of the origins of human autosomal inversionsTHOMAS, N. Simon; BRYANT, Victoria; MALONEY, Vivienne et al.Human genetics. 2008, Vol 123, Num 6, pp 607-616, issn 0340-6717, 10 p.Article

A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12YONGJIA YANG; JIHONG GUO; XIANGJUN XIAO et al.Human genetics. 2006, Vol 120, Num 1, pp 144-147, issn 0340-6717, 4 p.Article

Use of autosomal loci for clustering individuals and populations of East Asian originKIM, Jong-Jin; VERDU, Paul; PAKSTIS, Andrew J et al.Human genetics. 2005, Vol 117, Num 6, pp 511-519, issn 0340-6717, 9 p.Article

A mutagenesis scheme for obtaining autosomal mutations in DrosophilaSINGH, S.1983, Vol 21, Num 11, pp 635-636Article

A SPONTANEOUS CENTRIC FUSION HETEROZYGOTE IN THE TROPICAL GRASSHOPPER, VALANGA NIGROCORNIS (BURMEISTER)TEOH SB; YONG HS.1983; CARYOLOGIA; ITA; DA. 1983; VOL. 36; NO 2; PP. 165-173; BIBL. 13 REF.Article

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)SYX, Delfien; MALFAIT, Fransiska; VAN LAER, Lut et al.Human genetics. 2010, Vol 128, Num 1, pp 79-88, issn 0340-6717, 10 p.Article

Cognition genes on autosomes : the paradoxWILLEMS, P. J.Clinical genetics. 2007, Vol 72, Num 1, pp 9-12, issn 0009-9163, 4 p.Article

ON THE MORPHOLOGY OF Y AND OTHER CHROMOSOMES IN THE INDIAN FLYING FOX, PTEROPUS GIGANTEUS GIGANTEUS.MADHURI DATTA.1977; CURR. SCI.; INDIA; DA. 1977; VOL. 46; NO 19; PP. 687-688; BIBL. 3 REF.Article

AUTOSOMES AND TUMOURSGIORDANO A.1978; FOLIA HERED. PATHOL.; ITA; DA. 1978; VOL. 27; NO 4; PP. 65-74Article

CHROMOSOME SURFACE AREA. I. FURTHER EVIDENCE FOR AUTOSOMAL SEXUAL DIMORPHISMKOWALSKI CJ; NASJLETI CE; HARRIS JE et al.1978; EXPER. CELL RES.; USA; DA. 1978; VOL. 114; NO 2; PP. 397-402; BIBL. 10 REF.Article

SYNTHESE D'ADN DANS LES 2 PREMIERES PAIRES D'AUTOSOMES DE MOELLE OSSEUSE DE POULETTROFIMOVA LV; YAKOVLEV AF.1978; CITOL. I GENET., U.S.S.R.; S.S.S.R.; DA. 1978; VOL. 12; NO 2; PP. 125-129; ABS. ANGL.; BIBL. 11 REF.Article

ASPECTS GENETIQUES DES SITES FRAGILES AUTOSOMIQUES: A PROPOS DE 40 CASGUICHAOUA M; MATTEI MG; MATTEI JF et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 183-197; ABS. ENG; BIBL. 75 REF.Article

Construction of mouse A9 clones containing a single human chromosome (X/autosome translocation) via micro-cell fusionKOI, M; MORITA, H; SHIMIZU, M et al.Japanese journal of cancer research. 1989, Vol 80, Num 2, pp 122-125, issn 0910-5050Article

Autosomal fragile sites not a current indication for prenatal diagnosisHECHT, F; HECHT, B. K.Human genetics. 1984, Vol 67, Num 3, pp 352-353, issn 0340-6717Article

Coordinated replication timing of monoallelically expressed genes along human autosomesENSMINGER, Alexander W; CHESS, Andrew.Human molecular genetics (Print). 2004, Vol 13, Num 6, pp 651-658, issn 0964-6906, 8 p.Article

Epigenetic regulation of autosomal gene expression by sex chromosomesWIJCHERS, Patrick J; FESTENSTEIN, Richard J.Trends in genetics (Regular ed.). 2011, Vol 27, Num 4, pp 132-140, issn 0168-9525, 9 p.Article

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