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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

THREE CASES OF MINOR CHROMOSOMAL ABERRATIONS DISCOVERED BY PRENATAL CHROMOSOME DETERMINATION. = TROIS CAS D'ABERRATIONS CHROMOSOMIQUES MINEURES DECOUVERTS PAR L'ETUDE ANTENATALE DES CHROMOSOMESWAHLSTROM J.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 223-225; BIBL. 3 REF.Article

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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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

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Assignment¹ of p22 dynactin light chain (DCTN3) to human chromosome region 9p13 by radiation hybrid mappingMILLS, D. R; JACKSON, C. L.Cytogenetics and cell genetics. 2001, Vol 92, Num 1-2, issn 0301-0171, p. 166Conference Paper