kw.\*:("Cromosoma A1")
Results 1 to 25 of 1532
Selection :
Síndrome de microdeleción 1p36 = 1p36 microdeletion syndromeORTIGOSA GOMEZ, S; SEIDEL PADILLA, V; CUSCO, I et al.Anales de pediatria (2003. Ed. impresa). 2011, Vol 74, Num 3, pp 197-199, issn 1695-4033, 3 p.Article
Involvement of the TCL5 gene on human chromosome 1 in T-cell leukemia and melanomaFINGER, L. R; KAGAN, J; CHRISTOPHER, G et al.Proceedings of the National Academy of Sciences of the United States of America. 1989, Vol 86, Num 13, pp 5039-5043, issn 0027-8424Article
A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome IDRACOPOLI, N. C; STANGER, B. Z; ITO, C. Y et al.American journal of human genetics. 1988, Vol 43, Num 4, pp 462-470, issn 0002-9297Article
The DNA sequence and biological annotation of human chromosome 1GREGORY, S. G; BARLOW, K. F; JONES, M. C et al.Nature (London). 2006, Vol 441, Num 7091, pp 315-321, issn 0028-0836, 7 p.Article
Assignment of the human CD30 (Ki-1) gene to 1p36FONATSCH, C; LATZA, U; DÜRKOP, H et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 3, pp 825-826, issn 0888-7543Article
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin geneYOUSSOUFIAN, H; CHANCE, P; TUCK-MULLER, C. M et al.Human genetics. 1988, Vol 78, Num 3, pp 267-270, issn 0340-6717Article
A Locus on Chromosome 1 p36 Is Associated with Thyrotropin and Thyroid Function as Identified by Genome-wide Association StudyPANICKER, Vijay; WILSON, Scott G; SORANZO, Nicole et al.American journal of human genetics. 2010, Vol 87, Num 3, pp 430-435, issn 0002-9297, 6 p.Article
X chromosome-inactivation patterns of 1,005 phenotypically unaffected femalesAMOS-LANDGRAF, James M; COTTLE, Amy; PLENGE, Robert M et al.American journal of human genetics. 2006, Vol 79, Num 3, pp 493-499, issn 0002-9297, 7 p.Article
Report of the fifth international workshop on human chromosome 1 mapping 1999Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 143-171, issn 0301-0171Article
Assignment of CSRP1 encoding the LIM domain protein crp1, to human chromosome 1q32 by fluorescence in situ hybridizationERDEL, M; WEISKIRCHEN, R.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 10-11, issn 0301-0171Article
The IPP gene is assigned to human chromosome 1p32-1p22CHANG-YEH, A; WANG JABS, E; XIANG LI et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 239-241, issn 0888-7543Article
The human FCG1 gene encoding the high-affinity FcγRI maps to chromosome 1q21DIETSCH, E; OSMAN, N; MCKENZIE, I. F. C et al.Immunogenetics (New York, NY). 1993, Vol 38, Num 4, pp 307-309, issn 0093-7711Article
Localization of the human urate oxidase gene (UOX) to 1p22YELDANDI, A. V; PATEL, Y. D; LIAO, M et al.Cytogenetics and cell genetics. 1992, Vol 61, Num 2, pp 121-122, issn 0301-0171Article
Regional assignment of human tissue factor gene (F3) to chromosome 1p21-p22FA-TEN KAO; HARTZ, J; HORTON, R et al.Somatic cell and molecular genetics. 1988, Vol 14, Num 4, pp 407-410, issn 0740-7750Article
Human natriuretic peptides (ANP) gene locus: BsmI RFLPFROSSARD, P. M; COLEMAN, R. T; MORRISON, N. A et al.Nucleic acids research. 1987, Vol 15, Num 18, issn 0305-1048, 7656Article
A sequence-ready map of the human chromosome 1q telomereXIANG, Z; MORSE, E; HU, X.-L et al.Genomics (San Diego, Calif.). 2001, Vol 72, Num 1, pp 105-107, issn 0888-7543Article
Identification of microsatellite markers linked to the human leptin receptor gene on chromosome 1WINICK, J. D; STOFFEL, M; FRIEDMAN, J. M et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 1, pp 221-222, issn 0888-7543Article
A new VNTR polymorphism at locus D1S340HONMA, M; MITANI, K; MIZUSAWA, H et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, issn 0964-6906, p. 1329Article
Localization of the human TAX-1 gene to 1q32.1: a region implicated in microcephaly and Van der Woude syndromeKENWRICK, S; LEVERSHA, M; ROOKE, L et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, pp 1461-1462, issn 0964-6906Article
Localization of the gene-encoding upstream stimulatory factor (USF) to human chromosome 1q22-q23BIE-HUOY SHIEH; SPARKES, R. S; GAYNOR, R. B et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 1, pp 266-268, issn 0888-7543Article
Assignment of human prochymosin pseudogene to chromosome 1KOLMER, M; OÊRD, T; ALHONEN, L et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 2, pp 496-498, issn 0888-7543, 3 p.Article
Analysis of a scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12BLEYL, Steven B; BOTTO, Lorenzo D; CAREY, John C et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 21, pp 2368-2373, issn 1552-4825, 6 p.Article
Assignment1 of the human GABAA receptor delta-subunit gene (GABRD) to chromosome band 1p36.3 distal to marker NIB1364 by radiation hybrid mappingEMBERGER, W; WINDPASSINGER, C; PETEK, E et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 281-282, issn 0301-0171Article
Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridizationSPELEMAN, F; VAN CAMP, G; VAN ROY, N et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 189-190, issn 0301-0171Conference Paper
Human 60-kDa SS-A/Ro ribonucleoprotein autoantigen gene (SSA2) localized to 1q31 by fluorescence in situ hybridizationCHAN, E. K. L; TAN, E. M; WARD, D. C et al.Genomics (San Diego, Calif.). 1994, Vol 23, Num 1, pp 298-300, issn 0888-7543Article