FAMILIAL PARTIAL DISTAL 18Q (18Q22-18Q23) TRISOMYDE MUELENAERE A; FRYNS JP; VAN DEN BERGHE H et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 184-186; ABS. FRE; BIBL. 4 REF.Article

A CASE OF PARTIAL 3P TRISOMY (46,XY,-18,+DER(18),T(3; 18) (P24; Q22))TSUKINO R; OMORI H; UEMURA S et al.1981; PROC. JPN. ACAD., SER. B; ISSN 0386-2208; JPN; DA. 1981; VOL. 57; NO 3; PP. 89-94; BIBL. 8 REF.Article

TRISOMY 18 Q-. TRISOMY MAPPING OF CHROMOSOME 18 REVISITEDTURLEAU C; CHAVIN COLIN F; NARBOUTON R et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 1; PP. 20-26; BIBL. 11 REF.Article

TRISOMY 18QTER AND TRISOMY MAPPING OF CHROMOSOME 18.TURLEAU C; DE GROUCHY J.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 6; PP. 361-371; BIBL. 18 REF.Article

CONTRIBUTION A L'ETUDE DU CHROMOSOME 18 EN ANNEAU (A PROPOS DE DEUX OBSERVATIONS).WALLERICH THEOBALD MF.1977; ; S.L.; DA. 1977; PP. 1-82; BIBL. 25 P.; (THESE DOCT. MED.; NANCY I)Thesis

TETRASOMY 18 P: TENTATIVE DELINEATION OF A SYNDROMEBATISTA DAS; VIANNA MORGANTE AM; RICHIERI COSTA A et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 144-147; BIBL. 10 REF.Article

KARYOTYPE 47, XXY, 18P IN A NEWBORN CHILD WITH HOLOPROSENCEPHALYSCHNABEL R; HANSEN S.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 3; PP. 186-190; BIBL. 16 REF.Article

RING 18 MOSAICISM IN IDENTICAL TWINSHATA A; SUZUKI Y; MATSUI I et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 364-367; BIBL. 11 REF.Article

ANOMALIES CONSTITUTIONNELLES DU CHROMOSOME 18: MONOSOMIES PARTIELLES, ANNEAUX, TRISOMIE COMPLETE LIBRE. ETUDE DE CAS PERSONNELS ET REVUE DE LA LITTERATUREBRES MICHEL.1979; ; FRA; DA. 1979; 24; 88 P.: ILL.-PL.; 30 CM; BIBL. 61 REF.; TH.: MED./TOURS/1979Thesis

18 P - SYNDROME WITH A SINGLE CENTRAL MAXILLARY INCISORDOLAN LM; WILLSON WG.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 396-397; BIBL. 4 REF.Article

SYNDROMES ASSOCIATED WITH DELETION OF THE LONG ARM OF CHROMOSOME 18(DEL(18Q))WILSON MG; TOWNER JW; FORSMAN I et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 2; PP. 155-174; BIBL. 32 REF.Article

Un cas rare de mosaïcisme pour le chromosome 18 avec le caryotype 46, XX del (18) (p11)/46, XX, i (18 q)BADALYAN, L. O; MUTOVIN, G. R; MALYGINA, N. A et al.Genetika. 1983, Vol 19, Num 11, pp 1912-1915, issn 0016-6758Article

HYPERURICAEMIA ASSOCIATED WITH 18Q DELETION: ATYPICAL LESCH-NYHAN SYNDROME.LASZLO A; OSZTOVICS M; DALLMAN L et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 17-20; ABS. FRE; BIBL. 10 REF.Article

PARTIAL TRISOMY 13(Q14->QTER) DUE TO A FAMILIAL TRANSLOCATION T(13;18) (Q14;Q23)STEINBACH P.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

PARTIAL TRISOMY 18Q12, DUE TO INTRACHROMOSOMAL DUPLICATION, IS NOT ASSOCIATED WITH TYPICAL 18 TRISOMY PHENOTYPEFRYNS JP; VINKEN L; MARIEN J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 341-344; BIBL. 6 REF.Article

A DERIVATIVE CHROMOSOME 13 PAT IN A SUBJECT WITH MULTIPLE CONGENITAL ABNORMALITIES. REPOSITORY IDENTIFICATION NO GM-1224KOHN G; COHEN MM; ARONSON MM et al.1979; CYTOGENET. CELL. GENET.; CHE; DA. 1979; VOL. 24; NO 3; PP. 197; BIBL. 1 REF.Article

DAS 18 P- SYNDROM. = LE SYNDROME 18 P-AKSU F.1977; MONATSSCHR. KINDERHEILKDE; DTSCH.; DA. 1977; VOL. 125; NO 9; PP. 845-847; ABS. ANGL.; BIBL. 11 REF.Article

DEUX CAS DE TRISOMIE 10P PARTIELLE DUS A UNE TRANSLOCATION PATERNELLE T (10; 18) (P13; Q23).MORIC PETROVIC S; LACA Z; KRAJGHER A et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 3; PP. 195-197; ABS. ANGL.; BIBL. 11 REF.Article

PARTIAL TRISOMY 1Q AND MONOSOMY 18Q DUE TO A DE NOVO T(1;18)(Q25;Q23)SOLE MT; RIVERA H; SANCHEZ CORONA J et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 120-122; ABS. FRE; BIBL. 28 REF.Article

PERNICIOUS ANEMIA, 189 DELETION SYNDROME, AND IGA DEFICIENCYSTRICKER RB; LINKER CA.1982; JAMA, J. AM. MED. ASSOC.; ISSN 0098-7484; USA; DA. 1982; VOL. 248; NO 11; PP. 1359-1360; BIBL. 10 REF.Article

FAMILIAL CHROMOSOME TRANSLOCATION T(3;18) (P21; P11)BUCHINGER G; WETTSTEIN A; METZE H et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 2; PP. 119-123; BIBL. 5 REF.Article

DUPLICATION-DEFICIENCY OF A CHROMOSOME 18, RESULTING FROM RECOMBINATION OF A PATERNAL PERICENTRIC INVERSION, WITH A NOTE FOR GENETIC COUNSELLINGTEYSSIER JR; BAJOLLE F.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 195-200; BIBL. 22 REF.Article

FAMILIAL DICENTRIC TRANSLOCATION T(13;18) (P13;P11,2) ASCERTAINED BY RECURRENT MISCARRIAGESDANIEL A; PEREL ID; CLARKE AJ et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 73-75; BIBL. 8 REF.Article

NEW CHROMOSOMAL SYNDROMES. II: PARTIAL DISTAL 18 QTER TRISOMY SYNDROMEFRYNS JP; VAN DER HAUWAERT L; DUMOULIN M et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 3; PP. 217-219; BIBL. 15 REF.Article

DELETION SHORT ARM 18 AND SILVER-RUSSELL SYNDROME.CHRISTENSEN MF; NIELSEN J.1978; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1978; VOL. 67; NO 1; PP. 101-103; BIBL. 6 REF.Article