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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

BALANCED TRANSMISSION OF CENTROMERIC FISSION PRODUCTS IN MANFRYNS JP; BULCKE J; HENS L et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 127-128; BIBL. 7 REF.Article

Dinucleotide repeat polymorphism at the D10S469 locusDECKER, R. A; COLLINS, F. S.Human molecular genetics (Print). 1993, Vol 2, Num 8, issn 0964-6906, p. 1330Article

Assignment of the programmed cell death 4 gene (PDCD4) to human chromosome band 10q24 by in situ hybridizationSOEJIMA, H; MIYOSHI, O; YOSHINAGA, H et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 113-114, issn 0301-0171Article

A TRISOMY FOR 10924-QTER FROM A FAMILIAL TRANSLOCATION: T(4;10) (Q33;Q24) IN BOTH GRANDPARENTS.OSZTOVICS M; KASZAS T.1977; ACTA PAEDIATR. ACAD. SCI. HUNGAR.; HONGR.; DA. 1977; VOL. 18; NO 3-4; PP. 201-206; ABS. RUSSE; BIBL. 15 REF.Article

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

RING CHROMOSOME 10 ASSOCIATED WITH MULTIPLE CONGENITAL MALFORMATIONSSIMONI G; ROSSELLA F; DALPRA L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 117-121; BIBL. 8 REF.Article

TWO CASES OF PARTIAL TRISOMY 10Q IN THE SAME FAMILY CAUSED BY PARENTAL DIRECT INSERTION (INS. (15; 10) (Q15; Q24Q26))BACK E; KOSMUTZKY J; SCHUWALD A et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 195-198; ABS. FRE; BIBL. 19 REF.Article

GENE DOSAGE EFFECT. INTRABAND MAPPING OF HUMAN SOLUBLE GLUTAMIC OXALOACETIC TRANSAMINASESPRITZ RA; EMANUEL BS; CHERN CJ et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 23; NO 3; PP. 149-156; BIBL. 52 REF.Article

TRISOMY 10P DUE TO T(5; 10) (P15;P11) SEGREGATING IN A LARGE SIBSHIP.BACK E; VOGEL W; HERTE C et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 1; PP. 11-17; BIBL. 18 REF.Article

DEUX CAS DE TRISOMIE 10P PARTIELLE DUS A UNE TRANSLOCATION PATERNELLE T (10; 18) (P13; Q23).MORIC PETROVIC S; LACA Z; KRAJGHER A et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 3; PP. 195-197; ABS. ANGL.; BIBL. 11 REF.Article

Characterization of human genomic yeast artificial chromosome inserts containing hexokinase I coding information on chromosome 10GELB, B. D; WORLEY, K. C; GRIFFIN, L. D et al.Biochemical medicine and metabolic biology. 1992, Vol 47, Num 3, pp 265-269, issn 0885-4505Article

A polymorphic locus, D10S5, at 10q21.1MCDERMID, H. E; GOODFELLOW, P. J; DUNCAN, A. M. V et al.Nucleic acids research. 1987, Vol 15, Num 13, issn 0305-1048, 5498Article

Presence of a TaqI polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10HANAUER, A; MATTEI, M. G; MANDEL, J. L et al.Nucleic acids research. 1987, Vol 15, Num 15, issn 0305-1048, 6308Article

A fragile site 10q25 in human sperm chromosomesMARTIN, R. H.Journal of medical genetics. 1986, Vol 23, Num 3, issn 0022-2593, 279Article

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

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

Isolation and mapping of a polymorphic DNA sequence pTHH54 on chromosome 10 [D10S13]HOLM, T; NAKAMURA, Y; BALLARD, L et al.Nucleic acids research. 1988, Vol 16, Num 1, issn 0305-1048, 372Article

Isolation and mapping of a polymorphic DNA sequence pYNZ156 on chromosome 10 [D10S18]NAKAMURA, Y; CULVER, M; O'CONNELL, P et al.Nucleic acids research. 1988, Vol 16, Num 1, issn 0305-1048, 375Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 10RAY M; HUNTER AGW; JOSIFEK K et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 103-104; ABS. FRE; BIBL. 1 REF.Article

SERIAL DUPLICATION OF 10 (Q11->Q22) IN A PATIENT WITH MINOR CONGENITAL MALFORMATIONS.VOGEL W; BACK E; IMM W et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 159-163; BIBL. 15 REF.Article

THE DERMATOGLYPHIC PATTERN OF THE TRISOMY 10 P. SYNDROMERODEWALD A; STENGEL RUTKOWSKY S.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 6; PP. 330-337; BIBL. 22 REF.Article