Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4PINKEL, D; LANDEGENT, J; COLLINS, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 23, pp 9138-9142, issn 0027-8424Article

Heteromorphic variants of human chromosome 4BABU, A; VERMA, R. S.Cytogenetics and cell genetics. 1986, Vol 41, Num 1, pp 60-61, issn 0301-0171Article

Assignment of the human slit homologue SLIT2 to human chromosome band 4p15.2GEORGAS, K; BURRIDGE, L; SMITH, K et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 3-4, pp 246-247, issn 0301-0171Article

A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressedKANG LI; WARNER, C. K; HODGE, J. A et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 24, pp 13998-14004, issn 0021-9258, 7 p.Article

Assignment of CD38, the gene encoding human leukocyte antigen CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase), to chromosome 4p15NAKAGAWARA, K; MORI, M; OKAMOTO, H et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 1-2, pp 38-39, issn 0301-0171Conference Paper

Tentative assignment of piebald trait gene to chromosome band 4q12HOO, J. J; HASLAM, R. H. A; VAN ORMAN, C et al.Human genetics. 1986, Vol 73, Num 3, pp 230-231, issn 0340-6717Article

Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33TAINE, L; COUPRY, I; BOISSEAU, P et al.Human genetics. 1998, Vol 102, Num 2, pp 178-181, issn 0340-6717Article

The human HERC3 gene maps to chromosome 4q21 by fluorescence in situ hybridizationCRUZ, C; NADAL, M; VENTURA, F et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 263-264, issn 0301-0171Article

Toward the complete genomic map and molecular pathology of human chromosome 4RIESS, O; WINKELMANN, B; EPPLEN, J. T et al.Human genetics. 1994, Vol 94, Num 1, pp 1-18, issn 0340-6717Article

International workshop on human chromosome 4 mappingMYERS, R. M; VAN OMMEN, G.-J.Cytogenetics and cell genetics. 1994, Vol 66, Num 4, pp 217-236, issn 0301-0171Conference Proceedings

Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4HALL, C; MANSER, E; SPURR, N. K et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 2, pp 461-463, issn 0888-7543Article

Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1MORRISON, N; HARRAP, S. B; ARRIZA, J. L et al.Human genetics. 1990, Vol 85, Num 1, pp 130-132, issn 0340-6717, 3 p.Article

Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4 [HGM provisional no. D4S139]MILNER, E. C. B; LOTSHAW, C. L; VAN DIJK, K. W et al.Nucleic acids research. 1989, Vol 17, Num 10, issn 0305-1048, 4002Article

Un diagnostic cytogénétique difficile de monosomie 4p = A difficult prenatal diagnosis of 4p monosomyVITTU, G; CROQUETTE, M. F; BOIDEIN, F et al.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 75-82, issn 0021-7743Conference Paper

The human gene encoding SCYB9B, a putative novel CXC chemokine, maps to human chromosome 4q21 like the closely related genes for MIG (SCYB9) and INP10 (SCYB10)ERDEL, M; LAICH, A; UTERMANN, G et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 3-4, pp 271-272, issn 0301-0171Conference Paper

Interstitial deletion of the long arm of chromosome 4CHUDLEY, A. E; VERMA, M. R; RAY, M et al.American journal of medical genetics. 1988, Vol 31, Num 3, pp 549-551, issn 0148-7299Article

Chromosomal assignment of 20 cDNAs using flow-sorted spot-blot stampsGHISO, N. S; EVELETH, G. G; LIEUALLEN, K et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 570-572, issn 0888-7543Article

Dinucleotide repeat polymorphisms at the D4S126 and D4S114 lociTAGLE, D. A; BLANCHARD-MCQUATE, K. L; VALDES, J et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, issn 0964-6906, p. 1077Article

A third case of de novo partial trisomy 4 pOORTHUYS, J. W. E; GERSSEN-SCHOORL, K. B. J; DE PATER, J. M et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 344-345, issn 0022-2593, 2 p.Article

A rare heterochromatic variant of chromosome 4DOCHERTY, Z; BOWSER-RILEY, S. M.Journal of medical genetics. 1984, Vol 21, Num 6, pp 470-472, issn 0022-2593Article

Wolf-Hirschhorn (4p-) syndromeBATTAGLIA, Agatino; CAREY, John C; WRIGHT, Tracy J et al.Advances in pediatrics. 2001, Vol 48, pp 75-113, issn 0065-3101Article

Mild wolf-hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletionTITOMANLIO, L; ROMANO, A; CONTI, A et al.American journal of medical genetics. 2004, Vol 127A, Num 2, pp 197-200, issn 0148-7299, 4 p.Article

A major predisposition locus for severe obesity, at 4p15-p14STONE, Steven; ABKEVICH, Victor; POTTER, Jennifer et al.American journal of human genetics. 2002, Vol 70, Num 6, pp 1459-1468, issn 0002-9297Article

Assignment of the UGDH locus encoding UDP-glucose dehydrogenase to human chromosome band 4p15.1 by radiation hybrid mappingMARCU, O; STATHAKIS, D. G; MARSH, J. L et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 3-4, pp 244-245, issn 0301-0171Article

Chromosomal localization of the type-I 15-PGDH gene to 4q34-q35PICHAUD, F; DELAGE-MOURROUX, R; PIDOUX, E et al.Human genetics. 1997, Vol 99, Num 2, pp 279-281, issn 0340-6717Article