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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

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

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

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

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

Assignment of the L11 ribosomal protein gene (RPL11) to human chromosome 1p36.1→p35 by in situ hybridizationGRAPHODATSKY, A. S; VOROBIEVA, N. V; FILIPENKO, M. L et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 97-98, issn 0301-0171Article

Assignment of the human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43LESAGE, F; MATTEI, M.-G; FINK, M et al.Genomics (San Diego, Calif.). 1996, Vol 34, Num 1, pp 153-156, issn 0888-7543, 3 p.Article

APPARENTLY NON-DELETED RING-1 CHROMOSOME AND EXTREME GROWTH FAILURE IN A MENTALLY RETARDED GIRL.KJESSLER B; GUSTAVSON KH; WIGERTZ A et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 1; PP. 8-15; BIBL. 11 REF.Article

1p Microdeletion in sibs with minimal phenotypic manifestationsMARTINEZ, J. E; TUCK-MULLER, C. M; GASPARRINI, W et al.American journal of medical genetics. 1999, Vol 82, Num 2, pp 107-109, issn 0148-7299Article

A METHOD FOR THE MATHEMATICAL STUDY OF THE STAINED MASS OF THE CHROMOSOMES = UNE METHODE POUR L'ETUDE MATHEMATIQUE DE LA MASSE COLOREE DES CHROMOSOMESBODOR F; DAHLERUS B; GUSTAFSSON T et al.1974; HEREDETAS; SUEDE; DA. 1974; VOL. 77; NO 1; PP. 63-72; BIBL. 4 REF.Article

Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1THIENPONT, Bernard; DIMITRIADOU, Eftychia; THEODOROPOULOS, Katerina et al.European journal of medical genetics. 2009, Vol 52, Num 6, pp 393-397, issn 1769-7212, 5 p.Article

1q21-q22 Locus is associated with susceptibility to the reality-distortion syndrome of schizophrenia spectrum disordersROSA, A; FANANAS, L; CUESTA, M. J et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 516-518, issn 0148-7299Article

A BAC-based STS-content map spanning a 35-Mb region of human chromosome 1p35-p36YING ZHANG CHEN; HAYASHI, Yasuhide; MIZUSHIMA, Hiroshi et al.Genomics (San Diego, Calif.). 2001, Vol 74, Num 1, pp 55-70, issn 0888-7543Article

Searching for psoriasis susceptibility genes in Italy : Genome scan and evidence for a new locus on chromosome 1CAPON, F; NOVELLI, G; DALLAPICCOLA, B et al.Journal of investigative dermatology. 1999, Vol 112, Num 1, pp 32-35, issn 0022-202XConference Paper

Mapping of human potassium channel genes TREK-1 (KCNK2) and TASK (KCNK3) to chromosomes 1q41 and 2p23LESAGE, F; LAZDUNSKI, M.Genomics (San Diego, Calif.). 1998, Vol 51, Num 3, pp 478-479, issn 0888-7543Article

Refined chromosomal localization of the putative tumor suppressor gene TP73CUNSOLO, C. L; CASCIANO, I; BANELLI, B et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 3-4, pp 199-201, issn 0301-0171Article

Assignment of p53 binding protein (TP53BP2) to human chromosome band 1q42.1 by in situ hybridizationYANG, J.-P; ONO, T; SONTA, S et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 1, pp 61-62, issn 0301-0171Article

Assignment of the DNA fragmentation factor gene (DFFA) to human chromosome bands 1p36.3→p36.2 by in situ hybridizationLEEK, J. P; CARR, I. M; BELL, S. M et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 3-4, pp 212-213, issn 0301-0171Article

Assignment of the tenascin-R gene (Tnr) to mouse chromosome 4 band E2 by fluorescence in situ hybridization; refinement of the human TNR location to chromosome 1q24ARRIGO, G; GHERZI, R; BONAGLIA, M. C et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 2, pp 145-146, issn 0301-0171Article

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