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

Duplication 9q34 syndromeALLDERDICE, P. W; EALES, B; ONYETT, H et al.American journal of human genetics. 1983, Vol 35, Num 5, pp 1005-1019, issn 0002-9297Article

Two pericentric inversion inv (7) (p 15; d 32) and inv (9) (p 11; q 13) in a male with absence of vas deferensPETIT, P; FRYNS, J. P.Human genetics. 1983, Vol 64, Num 3, issn 0340-6717, 303Article

9p-syndrome: two new observationsSZYMARÍSKA, J; GUTKOWSKA, A; KUBALSKA, J et al.Klinische Pädiatrie. 1984, Vol 196, Num 2, issn 0300-8630, 121Article

A SUBTELOCENTRIC CHROMOSOME 9 IN A DYSPLASTIC 18-YEAR-OLD BOY WITH DISSOCIATED MENTAL DEVELOPMENT = CHROMOSOME 9 SUBTELOCENTRIQUE CHEZ UN GARCON DE 18 ANS DYSPLASIQUE AU DEVELOPPEMENT MENTAL DISSOCIEHANSMANN I; KEUTEL J.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 4; PP. 287-289; BIBL. 10 REF.Article

ON THE MONOCLONAL ORIGIN OF CHRONIC MYELOCYTIC LEUKEMIA. = SUR L'ORIGINE MONODONALE DE LA LEUCEMIE MYELOCYTAIRE CHRONIQUEHAYATA I; KAKATI S; SANDBERG AA et al.1974; PROC. JAP. ACAD.; JAP.; DA. 1974; VOL. 50; NO 5-6; PP. 381-385; BIBL. 10 REF.Article

INVERSION HOMOZYGOSITY OF CHROMOSOME NO.9 IN A HIGHLY INBRED KINDREDVINE DT; YARKONI S; COHEN MM et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 3; PP. 203-207; BIBL. 9 REF.Article

ASSOCIATION OF PERICENTRIC INVERSION OF CHROMOSOME 9 AND REPRODUCTIVE FAILURE IN TEN UNRELATED FAMILIESBOUE J; TAILLEMITE JL; HAZAEL MASSIEUX P et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 217-224; BIBL. 1 P.Article

X chromosome replication patterns in a case of X; 9 balanced translocationFILIPPI, G; PECILE, V; ARCHIDIACONO, N et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 467-468, issn 0022-2593Article

UNE NOUVELLE OBSERVATION DE CHROMOSOME 9 EN ANNEAUPORTNOL MF; VAN DEN AKKER J; LE PORRIER N et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 164-167; ABS. ENG; BIBL. 12 REF.Article

47, XY, T(9P+; 11Q+) IN A MALE INFANT WITH MULTIPLE MALFORMATIONS = , XY, T (9P+; 11Q+) CHEZ UN NOURRISSON MALE POLYMALFORMEDINNO ND; SILVEY GL; WEISSKOPF B et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 125-131; BIBL. 11REF.Article

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

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

A RING 9 CHROMOSOME. REPOSITORY IDENTIFICATION NO. GM-166KISTENMACHER ML; PUNNETT HH; ARONSON M et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 2; PP. 122-123; BIBL. 1 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

9P TRISOMY IDENTIFIED BY GIEMSA-11WYANDT HE; HECHT F; MAGENIS RE et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 355-358; BIBL. 8 REF.Article

PERICENTRIC INVERSIONS OF HUMAN CHROMOSOMES 9 AND 10 = INVERSIONS PERICENTRIQUES DES CHROMOSOMES HUMAINS 9 ET 10DE LA CHAPELLE A; SCHROEDER J; STENSTRAND K et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 26; NO 6; PP. 746-766; BIBL. 2P.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

MENTAL RETARDATION AND CONGENITAL MALFORMATIONS ASSOCIATED WITH A RING CHROMOSOME 9NAKAJIMA S; YANAGISAWA M; KAMOSHITA S et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 3; PP. 289-293; BIBL. 13 REF.Article

Tetrasomy 9p caused by idic (9) (pter→q13→pter)PONTES CAVALCANTI, D; FERRARI, I; CABRAL DE ALMEIDA, J. C et al.American journal of medical genetics. 1987, Vol 27, Num 3, pp 497-503, issn 0148-7299Article

Unusual chromosome 9 polymorphism and reproductive failureFRYNS, J. P; KLECZKOWSKA, A; LONDERS, L et al.Annales de génétique (Paris). 1985, Vol 28, Num 1, pp 49-51, issn 0003-3995Article

La monosomie 9P: à propos de deux observations = The 9P monosmy: about two casesCASTEL, Y; SIZUN, J; PARENT, P et al.Revue internationale de pédiatrie. 1985, Num 149, pp 21-28, issn 0048-8135Article

The phenotypic and cytogenetic spectrum of partial trisomy 9WILSON, G. N; RAJ, A; BAKER, D et al.American journal of medical genetics. 1985, Vol 20, Num 2, pp 277-282, issn 0148-7299Article

A CASE OF PARTIAL GP MONOSOMY WITH SOME UNUSUAL CLINICAL FEATURES.RUTTEN FJ; HUSTINX TWJ; DUNK TILLEMANS AAW et al.1978; ANN. GENET.; FR.; DA. 1978; VOL. 21; NO 1; PP. 51-55; ABS. FR.; BIBL. 19 REF.Article

THE DISTAL 9P TRISOMY SYNDROME: A MAJOR CLINICAL-CYTOGENETIC ENTITY.CENTERWALL WR.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3D; PP. 165-177; BIBL. 6 REF.Article