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

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

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

ANNEAU DU CHROMOSOME 4. II. SANS DYSMORPHIE FACIALE.CHAVIN COLIN F; TURLEAU C; LIMAL JM et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 105-109; ABS. ANGL.; BIBL. 12 REF.Article

RING CHROMOSOME-4.MCDERMOTT A; VOYCE MA; ROMAIN D et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 3; PP. 228-232; BIBL. 4 REF.Article

RING CHROMOSOME 4 AND WOLF SYNDROME.PEREZ CASTILLO A; ABRISQUETA JA.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 1; PP. 87-91; BIBL. 9 REF.Article

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

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

Assignment of dentin sialophosphoprotein (DSPP) to the critical DGI2 locus on human chromosome 4 band q21.3 by in situ hybridizationMACDOUGALL, M; SIMMONS, D; LUAN, X et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 1-2, pp 121-122, issn 0301-0171Conference Paper

Chromosomal mapping of cell death proteases CPP32, MCH2, and MCH3BULLRICH, F; FERNANDES-ALNEMRI, T; LITWACK, G et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 2, pp 362-365, issn 0888-7543Article

Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4ZASLAV, Ann-Leslie; PIERNO, Guy; FOUGNER, Arthur et al.American journal of medical genetics. 2004, Vol 126A, Num 4, pp 420-422, issn 0148-7299, 3 p.Article

Targeted construction of a high-resolution, integrated, comprehensive, and comparative map for a region specific to bovine chromosome 6 based on radiation hybrid mappingWEIKARD, Rosemarie; KÜHN, Christa; GOLDAMMER, Tom et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 6, pp 768-776, issn 0888-7543Article

Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecBDUFFY, David L; MONTGOMERY, Grant W; HALL, Jeff et al.American journal of medical genetics. 2001, Vol 100, Num 3, pp 182-186, issn 0148-7299Article

Assignment of GRINL1B, a glutamate receptor-like processed gene, to human chromosome 4q12 by in situ hybridizationMOHAN RAJ, B. K; ROGINSKI, R. S; FINKERNAGEL, S. W et al.Cytogenetics and cell genetics. 2001, Vol 95, Num 3-4, pp 238-239, issn 0301-0171Article

Localization of the ribonuclease L inhibitor gene (RNSAI), a new member of the interferon-regulated 2-5A pathway, to 4q31 by fluorescence in situ hybridizationDIRIONG, S; SALEHZADA, T; BISBAL, C et al.Genomics (San Diego, Calif.). 1996, Vol 32, Num 3, pp 488-490, issn 0888-7543Article

Assignment of GRSF1 encoding a poly(A)⁺ mRNA binding protein to human chromosome 4q13BANGA, S. S; OZER, H. L; WILUSZ, J et al.Cytogenetics and cell genetics. 1996, Vol 73, Num 4, pp 295-296, issn 0301-0171Conference Paper

Familial 25.3 Mb Inverted Duplication of Bands q32.1 to q35.1 on Chromosome 4 With Psychomotor ImpairmentsMARTIN, Judith; SALEKI, Reza; CHRISTENSEN, Todd et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2624-2628, issn 1552-4825, 5 p.Article

Pre-and Postnatal Overgrowth in a Patient With Proximal 4p DeletionLINGQIAN WU; ZHIGAO LONG; DESHENG LIANG et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 6, pp 791-794, issn 1552-4825, 4 p.Article

Familial interstitial deletion of chromosome 4 (p15.2p16.1)TONK, Vijay S; JALAL, Syed M; GONZALEZ, Jose et al.Annales de génétique (Paris). 2003, Vol 46, Num 4, pp 453-458, issn 0003-3995, 6 p.Article

Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridizationSAITO-OHARA, F; UCHIDA, S; TAKEUCHI, Y et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 2, pp 372-374, issn 0888-7543Article