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DELETION IN THE SHORT ARM OF CHROMOSOME 9 FROM A SUBJECT WITH CONGENITAL CEREBRAL MALDEVELOPMENT. REPOSITORY IDENTIFICATION NO. GM-870.BREG WR; ARONSON MM; HILL R et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 5; PP. 296-297; BIBL. 1 REF.Article

DUPLICATION OF THE SHORT ARM OF CHROMOSOME 9. ANALYSIS OF FIVE CASESCUOCO C; GIMELLI G; PASQUALI F et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 3-7; BIBL. 22 REF.Article

CYTOGENETIQUE D'UN PATIENT PORTEUR DE DELETION DES CONSTRICTIONS SECONDAIRES DU CHROMOSOME 9 ET ETUDE FAMILIALEHE XIAOXUAN; XIA JIAHUI; LI LUYUN et al.1982; YICHUAN XUEBAO. (ACTA GENETICA SINICA); ISSN 0379-4172; CHN; DA. 1982; VOL. 9; NO 4; PP. 315-319; ABS. ENG; BIBL. 12 REF.Article

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TRISOMY OF THE SHORT ARM OF CHROMOSOME NUMBER 9: A CLINICAL ENTITYFRYNS JP; VAN DEN BERGHE H.1980; ACTA PAEDIATR. BELG.; BEL; DA. 1980; VOL. 33; SUPPL.; 8 P.; BIBL. 5 REF.Article

PERICENTRIC INVERSIONS OF CHROMOSOME NUMBER 9: BENIGN OR HARMFUL.HOWARD PEEBLES PN; STODDARD GR.1979; HUM. HERED.; CHE; DA. 1979; VOL. 29; NO 2; PP. 111-117; BIBL. 2 P.Article

THE DERMATOGLYPHIC PATTERN OF THE TRISOMY 9P SYNDROMERODEWALD A; STENGEL RUTKOWSKI S; ZANKL M et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 6; PP. 405-417; BIBL. 2 P.Article

TRISOMY 9P WITH AN ISOCHROMOSOME OF 9PSMITH G; MCCAA A; KELLY TE et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 125-126; BIBL. 15 REF.Article

PRESENCE, CHEZ UN HOMME STERILE, DE DEUX INVERSIONS PERICENTRIQUES DES CHROMOSOMES 9: INV(9) (P11Q1209), INV(9) (PTER1209)CROQUETTE MF; COUTURIER J; DUTRILLAUX B et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 1; PP. 53-56; ABS. ENG; BIBL. 11 REF.Article

LANG. ENGPAULI RM; PAGON RA; HALL JG et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 297-301; BIBL. 25 REF.Article

PARTIAL TETRASOMY 9 IN A LIVEBORN INFANTWISNIEWSKI L; POLITIS GD; HIGGINS JV et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 147-153; BIBL. 8 REF.Article

ANOTHER CASE OF 9P-SYNDROME.MULCAHY MT.1978; ANN. GENET.; FR.; DA. 1978; VOL. 21; NO 1; PP. 47-49; ABS. FR.; BIBL. 5 REF.Article

GENETICS OF THE +P9 SYNDROME.LURIE IW; LAZJUK GI; GUREVICH DB et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 1; PP. 23-33; BIBL. 2 P.Article

TETRASOMY 9P: CLINICAL ASPECTS AND ENZYMATIC GENE DOSAGE EXPRESSIONGARCIA CRUZ D; VACA G; IBARRA B et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 4; PP. 237-242; ABS. FRE; BIBL. 12 REF.Article

THE TRISOMY 9 SYNDROMECARPENTER BF; TOMKINS DJ.1982; PERSPECTIVES IN PEDIATRIC PATHOLOGY; ISSN 0091-2921; USA; DA. 1982; VOL. 7; PP. 109-120; BIBL. 43 REF.Article

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

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DERMATOGLYPHIC PATTERNS IN 9P TRISOMY SYNDROME.LOESCH D; CZYZEWSKA J.1978; J. MENTAL DEFIC. RES.; G.B.; DA. 1978; VOL. 22; NO 1; PP. 49-68; BIBL. 10 REF.Article