Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Autosoma")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 458

  • Page / 19
Export

Selection :

  • and

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

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

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

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

The T-box transcription factor SEA-1 is an autosomal element of the X:A signal that determines C. elegans sexPOWELL, Jennifer R; JOW, Margaret M; MEYER, Barbara J et al.Developmental cell. 2005, Vol 9, Num 3, pp 339-349, issn 1534-5807, 11 p.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

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

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreousPRASOV, Lev; MASUD, Tehmina; KELBERMAN, Daniel et al.Human molecular genetics (Print). 2012, Vol 21, Num 16, pp 3681-3694, issn 0964-6906, 14 p.Article

The different levels of genetic diversity in sex chromosomes and autosomesELLEGREN, Hans.Trends in genetics (Regular ed.). 2009, Vol 25, Num 6, pp 278-284, issn 0168-9525, 7 p.Article

Mortality risks in patients with constitutional autosomal chromosome deletions in Britain : a cohort studySWERDLOW, Anthony J; SCHOEMAKER, Minouk J; HIGGINS, Craig D et al.Human genetics. 2008, Vol 123, Num 2, pp 215-224, issn 0340-6717, 10 p.Article

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3KHAN, Shahid Y; RIAZUDDIN, Saima; RIAZUDDIN, Sheikh et al.Human genetics. 2007, Vol 120, Num 6, pp 789-793, issn 0340-6717, 5 p.Article

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)KLEIN, Christoph; GRUDZIEN, Magda; BOHN, Georg et al.Nature genetics. 2007, Vol 39, Num 1, pp 86-92, issn 1061-4036, 7 p.Article

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2SANTOS, Regie Lyn P; MUHAMMAD JAWAD HASSAN; SIKANDAR, Shaheen et al.Human genetics. 2006, Vol 120, Num 1, pp 85-92, issn 0340-6717, 8 p.Article

Comparative chromosome painting of chicken autosomal paints 1-9 in nine different bird speciesGUTTENBACH, M; NANDA, I; FEICHTINGER, W et al.Cytogenetic and genome research. 2003, Vol 103, Num 1-2, pp 173-184, issn 1424-8581, 12 p.Article

La perfusion autorégulée et autoprogrammée appliquée en obstétrique, en endocrinologie et en sexologie = Self-regulated and self programmed infusion applied to obstetrics, endocrinology and sexologyBAUDEU, H.Techniques hospitalières médico-sociales et sanitaires. 1983, Vol 38, Num 459, pp 121-122, issn 0040-1374Article

An autosomal locus that controls chromosomewide replication timing and mono-allelic expressionSTOFFREGEN, Eric P; DONLEY, Nathan; STAUFFER, Daniel et al.Human molecular genetics (Print). 2011, Vol 20, Num 12, pp 2366-2378, issn 0964-6906, 13 p.Article

Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23―22.3NAZ, Gul; ALI, Ghazanfar; SYED KAMRAN-UL-HASSAN NAQVI et al.Human genetics. 2010, Vol 127, Num 4, pp 395-401, issn 0340-6717, 7 p.Article

Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosisDEVONALD, Mark A. J; SMITH, Annabel N; POON, Jenny P et al.Nature genetics. 2003, Vol 33, Num 2, pp 125-127, issn 1061-4036, 3 p.Article

Malformations and minor anomalies in non-trisomic, autosomal aneuploidyCUNNIFF, C; POPE, S. K.American journal of medical genetics. 1993, Vol 47, Num 4, pp 556-558, issn 0148-7299Article

The relative rates of evolution of sex chromosomes and autosomesCHARLESWORTH, B; COYNE, J. A; BARTON, N. H et al.The American naturalist. 1987, Vol 130, Num 1, pp 113-146, issn 0003-0147Article

The Autosomal Recessive Cerebellar AtaxiasANHEIM, Mathieu; TRANCHANT, Christine; KOENIG, Michel et al.The New England journal of medicine. 2012, Vol 366, Num 7, pp 636-646, issn 0028-4793, 11 p.Article

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaGUERNSEY, Duane L; HAIYAN JIANG; SAINT-AMANT, Louis et al.Nature genetics. 2009, Vol 41, Num 6, pp 651-653, issn 1061-4036, 3 p.Article

  • Page / 19