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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

POLYMORPHISM OF CHROMOSOME 9 IN 600 GREEK SUBJECTS.METAXOTOU C; KALPINI MAVROU A; PANAGOU M et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 30; NO 1; PP. 85-89; BIBL. 13 REF.Article

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

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

L'INSTABILITE PSYCHO-MOTRICE EST-ELLE VRAIMENT UN SIGNE CARACTERISTIQUE DE LA TRISOMIE 9P.: A PROPOS DE 3 OBSERVATIONSLE MAREC B; BOUCHARD C; BOIXEL J et al.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 3; PP. 263-269; ABS. ENG; BIBL. 8 REF.Article

TRISOMY 9 SYNDROMEANNEREN G; SEDIN G.1981; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1981; VOL. 70; NO 1; PP. 125-128; BIBL. 17 REF.Article

EXPRESSION OF GALT IN 9P CHROMOSOME ALTERATIONS: ASSIGNMENT OF GALT LOCUS TO 9CEN->9P22SPARKES RS; SPARKES MC; FUNDERBURK SJ et al.1980; ANN. HUM. GENET.; GBR; DA. 1980; VOL. 43; NO 4; PP. 343-347; BIBL. 8 REF.Article

CHROMOSOMAL VARIANTS AND NONDISJUNCTION.FORD JH; LESTER P.1978; CYTOGENET. CELL. GENET.; CHE; DA. 1978; VOL. 21; NO 5; PP. 300-303; BIBL. 10 REF.Article

PROBABLE LINKAGE BETWEEN THE HUMAN GALACTOSE-1-P URIDYL TRANSFERASE LOCUS AND 9QHSPARKES RS; EPSTEIN PA; KIDD KK et al.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 2; PP. 188-193; BIBL. 29 REF.Article

UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTINOI MF; VAN DEN AKKER J; LE PORRIER N et al.1983; SEMAINE DES HOPITAUX; ISSN 0037-1777; FRA; DA. 1983; VOL. 59; NO 3; PP. 185-188; ABS. ENG; BIBL. 12 REF.Article

TWO UNUSUAL G-BAND VARIANTS OF THE PHORT ARM OF CHROMOSOME 9SUTHERLAND GR; EYRE H.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 5; PP. 331-334; BIBL. 7 REF.Article

WHERE IS THE GENE FOR GALTMULCAHY MT; WILSON RG.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 1; PP. 129-130; BIBL. 15 REF.Article

COMPLETE DEFICIENCY OF CONSTITUTIVE HETEROCHROMATIN ON A HUMAN CHROMOSOME 9BUYS CHCM; YPMA JMM; GOUW WL et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 129-132; BIBL. 8 REF.Article

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

MAPPING AK1, ACONS, AND AK3 TO CHROMOSOME 9 IN MAN EMPLOYING AN X/9 TRANSLOCATION AND SOMATIC CELL HYBRIDS.SHOWS TB; BROWN JA.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 19; NO 1; PP. 26-37; BIBL. 2 P. 1/2Article

LOCALISATION OF THE HUMAN ABO: NP-1:AK-1 LINKAGE GROUP BY REGIONAL ASSIGNMENT OF AK-1 TO 9Q34.FERGUSON SMITH MA; AITKEN DA; TURLEAU C et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 1; PP. 35-43; BIBL. 1 P. 1/2Article

INTERACTIONS BETWEEN C-BANDS OF CHROMOSOMES 1 AND 9 IN RECURRENT REPRODUCTIVE LOSSFORD JH; CALLEN DF; ROBERTS CG et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 58-62; BIBL. 8 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

THE DERMATOGLYPHIC AND CLINICAL FEATURES OF THE 9P TRISOMY AND PARTIAL 9P MONOSOMY SYNDROMESYOUNG RS; REED T; HODES ME et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 1; PP. 31-39; BIBL. 15 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

DELETION OF THE SHORT ARM OF CHROMOSOME 9. A CLINICALLY RECOGNISABLE ENTITYFRYNS JP; PEDERSEN JC; DUYCK H et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 3; PP. 201-204; BIBL. 15 REF.Article

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

VARIABILITE DES REGIONS HETEROCHROMATIQUES DES CHROMOSOMES HUMAINS 1, 9, 16 ET YPODUGOL'NIKOVA OA; SUSHANLO KH M; PARFENOVA IV et al.1980; GENETIKA; SUN; DA. 1980; VOL. 16; NO 4; PP. 720-726; H.T. 1; ABS. ENG; BIBL. 23 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

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