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An integrated map of chromosome 9COLLINS, A; FORABOSCO, P; LAWRENCE, S et al.Annals of human genetics. 1995, Vol 59, pp 393-402, issn 0003-4800, 4Conference Paper

PERICENTRIC INVERSION, INV (9) (P22 Q32), IN THE FATHER OF A CHILD WITH A DUPLICATION-DELETION OF CHROMOSOME 9 AND GENE DOSAGE EFFECT FOR ADENYLATE KINASE-1MATTEI JF; MATTEI MG; ARDISSONE JP et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 2; PP. 129-136; BIBL. 13 REF.Article

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TYPE AND CONTRETYPE SIGNS IN MONOSOMY AND TRISOMY 9P: ON A CASE 46,XY,DEL(9) (PTER->P12:)HERNANDEZ A; RIVERA H; JIMENEZ SAINZ M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 3; PP. 155-157; ABS. FRE; BIBL. 13 REF.Article

Tetrasomy 9p confirmed by GALTBALESTRAZZI, P; CROCI, G; FRASSI, C et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 396-399, issn 0022-2593Article

CONTRIBUTION A L'ETUDE DES DELETIONS DU CHROMOSOME 9. UNE OBSERVATION PERSONNELLE DE CHROMOSOME 9 EN ANNEAU ET UNE OBSERVATION PERSONNELLE D'UN CHROMOSOME 9PCOCHET MARIE ANNE.1979; ; FRA; LYON: ASSOCIATION AMICALE ETUD. PHARM.; DA. 1979; 47; 30 CM; BIBL. 86 REF.; TH.: MED./LYON 1/1979Thesis

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A nasty hex on chromosome 9 causes FTD/ALSCONNOLLY, C.Clinical genetics. 2012, Vol 81, Num 2, pp 126-127, issn 0009-9163, 2 p.Article

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Confirmation of 9q34 as the chromosomal site of the human lipocalin LCN1 geneHERZOG, H; BAUMGARTNER, M; HOLZFEIND, P et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 1-2, pp 108-109, issn 0301-0171Conference Paper

Hypomethylation of human heterochromatin detected by restriction enzyme nick translationMITCHELL, A. R.Experimental cell research. 1992, Vol 202, Num 1, pp 203-206, issn 0014-4827Article

The structural gene for aldolase B(ALDB) maps to 9qk3→32HENRY, I; GALLANO, P; BESMOND, C et al.Annals of human genetics. 1985, Vol 49, Num 3, pp 173-180, issn 0003-4800Article

MODERATE MENTAL RETARDATION AND NONSPECIFIC DYSMORPHIC SYNDROME ASSOCIATED WITH RING CHROMOSOME 9FRYNS JP; LAMBRECHTS A; JANSSEUNE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 29-32; BIBL. 15 REF.Article

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PARTIAL 9Q TRISOMY ASSOCIATED WITH A 9,21 TRANSLOCATION.CHAMLA Y; BILBEISSI C; MICHEAU M et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 2; PP. 245-248; BIBL. 7 REF.Article

LA TRISOMIE 9P. UN CAS DE TRANSLOCATION T(9;22) (P11;P11)-MAT CHEZ UNE FILLETTE.GENEST P; ROUSSY J; GENEST FB et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 7; PP. 956-959; ABS. ANGL.; BIBL. 14 REF.Article

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A PERICENTRIC INVERSION OF CHROMOSOME 9 AND A REARRANGEMENT INVOLVING CHROMOSOMES 9 AND 10 OBSERVED IN TWO GENERATIONS. CLINICAL DESCRIPTION OF CHROMOSOME 9 (P12-P21) DELATION SYNDROMEFALLSTROM SP; WAHLSTROM J.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 480-486; BIBL. 14 REF.Article

INTERCHROMOSOMAL DUPLICATION FOR THE SHORT ARM OF CHROMOSOME NO. 9: REPORT OF THREE CASES DUE TO A FAMILIAL TRANSLOCATION T(9; 11) AND ONE CASE WITH A DE NOVO 47, XX, +9P KARYOTYPE.LIN CC; HOLMAN G; SEWELL L et al.1977; J. MENTAL DEFIC. RES.; G.B.; DA. 1977; VOL. 21; NO 4; PP. 309-320; BIBL. 1 P. 1/2Article

Human chromosome 9 pericentric homologies : implications for chromosome 9 heteromorphismsPARK, J. P; WOJISKI, S. A; SPELLMAN, R. A et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 3-4, pp 192-194, issn 0301-0171Article