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A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26CICHON, S; SCHMIDT-WOLF, G; FRITZE, J et al.Molecular psychiatry. 2001, Vol 6, Num 3, pp 342-349, issn 1359-4184Article

Mapping of the human ribosomal small subunit protein gene RPS24 to the chromosome 10q22-q23 boundaryJONES, A.-M; MARZELLA, R; ROCCHI, M et al.Genomics (San Diego, Calif.). 1997, Vol 39, Num 1, pp 121-122, issn 0888-7543Article

Assignment of the closet human homologue (DNA2L; KIAA0083) of the yeast Dna2 helicase gene to chromosome band 10q21.3-q22.1EKI, T; OKUMURA, K; SHIRATORI, A et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 3, pp 408-410, issn 0888-7543Article

Assignment of the human prosaposin gene (PSAP) to 10q22.1 by fluorescence in situ hybridizationBAR-AM, I; AVIVI, L; HOROWITZ, M et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 4, pp 316-318, issn 0301-0171Conference Paper

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Interstitial deletion del(10)(q25.2q25.3 ∼ 26.11) : case report and review of the literatureKEHRER-SAWATZKI, Hildegard; DAUMILLER, Eva; MÜLLER-NAVIA, Jutta et al.Prenatal diagnosis. 2005, Vol 25, Num 10, pp 954-959, issn 0197-3851, 6 p.Article

Localization of the gene (TAF2D) encoding the 100-kDa subunit (hTAF_II100) of the human TFIID complex to chromosome 10 band q24-q25.2DUBROVSKAYA, V; MATTEI, M.-G; TORA, L et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 3, pp 556-557, issn 0888-7543Article

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RING 10 CHROMOSOME: 46, XX, R10 (P15 Q26)SPARKES RS; LING SM; MULLER H et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 341-345; BIBL. 16 REF.Article

Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanomaGULDBERG, P; THOR STRATEN, P; BIRCK, A et al.Cancer research (Baltimore). 1997, Vol 57, Num 17, pp 3660-3663, issn 0008-5472Article

HTRA1 promoter polymorphism in wet age-related macular degenerationDEWAN, Andrew; MUGEN LIU; BARNSTABLE, Colin et al.Science (Washington, D.C.). 2006, Vol 314, Num 5801, pp 989-992, issn 0036-8075, 4 p.Article

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

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolutionCHENG, Jill; KAPRANOV, Philipp; SEMENTCHENKO, Victor et al.Science (Washington, D.C.). 2005, Vol 308, Num 5725, pp 1149-1154, issn 0036-8075, 6 p.Article

PTEN and MXI1 allelic loss on chromosome 10q is rare in melanoma in vivoHERBST, R. A; PODEWSKI, E. K; MOMMERT, S et al.Archives of dermatological research (Print). 1999, Vol 291, Num 10, pp 567-569, issn 0340-3696Article

Assignment of the human ADP-ribosylation factor-like 3 (ARL3) gene to chromosome 10 band q23.3 by radiation hybrid mappingKIM, H.-S.Cytogenetics and cell genetics. 1998, Vol 83, Num 3-4, issn 0301-0171, p. 246Conference Paper

Assignment of human genes for β2 and β4 subunits of voltage-dependent Ca²⁺ channels to chromosomes 10p12 and 2q22-q23TAVIAUX, S; WILLIAMS, M. E; HARPOLD, M. M et al.Human genetics. 1997, Vol 100, Num 2, pp 151-154, issn 0340-6717Article

Assignment of the human gene encoding the Δ¹-pyrroline-5-carboxylate synthetase (P5CS) to 10q24.3 by in situ hybridizationLIU, G; MAUNOURY, C; KAMOUN, P et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 1, pp 145-146, issn 0888-7543Article

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Aalzheimer diseaseGRUPE, Andrew; YONGHONG LI; TACEY, Kristina et al.American journal of human genetics. 2006, Vol 78, Num 1, pp 78-88, issn 0002-9297, 11 p.Article

Report of the Third International Workshop on Human Chromosome 10 Mapping and Sequencing 1999DELOUKAS, P; FRENCH, L; MEITINGER, T et al.Cytogenetics and cell genetics. 2000, Vol 90, Num 1-2, pp 1-12, issn 0301-0171Article

Assignment of SUPV3L1 to human chromosome band 10q22.1 by in situ hybridizationDMOCHOWSKA, A; STANKIEWICZ, P; GOLIK, P et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 84-85, issn 0301-0171Article

Assignment of the p150 subunit of the eukaryotic initiation factor 3A gene (EIF3A) to human chromosome band 10q26 by in situ hybridisationENSINGER, C; OBRIST, P; MIKUZ, G et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 74-75, issn 0301-0171Article

Assignment of candidate DNA methyltransferase gene (DNMT2) to human chromosome band 10p15.1 by in situ hybridizationVILAIN, A; APIOU, F; DUTRILLAUX, B et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 1-2, issn 0301-0171, p. 120Conference Paper

Q(Q23->QTER) DUPLICATION: GOTS, HK1, AND OTHER GENE MARKERS.SPARKES RS; BASS; SPARKES MC et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 267-270; BIBL. 6 REF.Article

Complete Trisomy 10p Resulting From an Extra Stable Telocentric ChromosomeLOZIC, Bernarda; CULIC, Vida; LASAN, Ruzica et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 7, pp 1778-1781, issn 1552-4825, 4 p.Article