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THE R(20) SYNDROME.HERVA R; SAARINEN I; LEIKKONEN L et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 281-283; BIBL. 5 REF.Article

A(14;20) BALANCED TRANSLOCATION, 46, XX. REPOSITORY IDENTIFICATION NO. GM-982.EMANUEL BS; ZACKAI E; MELLMAN WJ et al.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 21; NO 3; PP. 174Article

A(14;20) TRANSLOCATION, UNBALANCED, FROM A SUBJECT WITH SEVERE CONGENITAL ANOMALIES. REPOSITORY IDENTIFICATION NO. GM-981.EMANUEL BS; ZACKAI E; MELLMAN WJ et al.1978; CYTOGENET. CELL GENET.; SWITZ.; DA. 1978; VOL. 21; NO 3; PP. 173Article

FAMILIAL TRISOMY 20 P. FIVE CASES AND TWO CARRIERS IN THREE GENERATIONS. A REVIEW.CENTERWALL W; FRANCKE U.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 77-83; ABS. FR.; BIBL. 11 REF.Article

ANOMALIE CHROMOSOMIQUE NOUVELLE PAR TRANSLOCATION T (20;22) AU COURS D'UNE LEUCEMIE MYELOIDE CHRONIQUELAI JL; JOUET JP; BAUTERS F et al.1982; NOUVELLE PRESSE MEDICALE; ISSN 0301-1518; FRA; DA. 1982; VOL. 11; NO 44; PP. 3270; BIBL. 3 REF.Article

REGIONAL ASSIGNMENT OF THE ADA LOCUS ON 20 Q 13.2->QTER BY GENE DOSAGE STUDIESPHILIP T; LENOIR G; ROLLAND MO et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 2-3; PP. 187-189; BIBL. 9 REF.Article

CHROMOSOMAL MARKER 20Q- IN CASES OF OSTEOMYELOSCLEROSIS AND CMLFLEISCHMAN EW; PRIGOGINA EL; VOLKOVA MA et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 1; PP. 101-104; BIBL. 9 REF.Article

CHROMOSOME 20 EN ANNEAU: UN NOUVEAU SYNDROME.JALBERT P; JALBERT H; SELE B et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 258-262; ABS. ANGL.; BIBL. 24 REF.Article

De novö trisomy 20p with macroorchidism in a prepubertal boyBALESTRAZZI, P; VIRDIS, R; FRASSI, C et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 58-59, issn 0003-3995Article

Del(20p) with manifestations of arteriohepatic dysplasiaBYRNE, J. L. B; HARROD, M. J. E; FRIEDMAN, J. M et al.American journal of medical genetics. 1986, Vol 24, Num 4, pp 673-678, issn 0148-7299Article

Alagille syndrome with de Novo del(20) (p11.2)TEEBI, A. S; KRISHNA MURTHY, D. S; ISMAIL, E. A. R et al.American journal of medical genetics. 1992, Vol 42, Num 1, pp 35-38, issn 0148-7299Article

Ring 20 chromosome phenotypePORFIRIO, B; VALORANI, M. G; GIANNOTTI, A et al.Journal of medical genetics. 1987, Vol 24, Num 6, pp 375-377, issn 0022-2593Article

A DELETION IN CHROMOSOME 22 CAN CAUSE DIGEORGE SYNDROMEDE LA CHAPELLE A; HERVA R; KOIVISTO M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 3; PP. 253-256; BIBL. 20 REF.Article

CHROMOSOMAL DNA CYTOPHOTOMETRY IN 20 Q-NONSPECIFIC MYELOID DISORDERSCARRANO AV; MAYALL BH; TESTA JR et al.1979; CANCER RES.; USA; DA. 1979; VOL. 39; NO 8; PP. 2984-2987; BIBL. 25 REF.Article

TRISOMY FOR THE DISTAL THIRD OF THE LONG ARM OF CHROMOSOME 19 IN BROTHER AND SISTERSCHMID W.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 263-270; BIBL. 1 REF.Article

DELECTION OF THE SHORT ARMS OF CHROMOSOME 20.KALOUSEK DK; THERIEN S.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 1; PP. 89-92; BIBL. 8 REF.Article

TRANSLOCATION T(1;20)(Q21;Q13) IN AN AZOOSPERMIC MANANTONELLI A; DEL MARCO A; GABELLINI P et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 151; BIBL. 3 REF.Article

TRIPLICATION OF CHROMOSOME ARM 20 P DUE TO INHERITED TRANSLOCATION AND SECONDARY NONDISJUNCTIONMARCUS ES; FULLER B; RICCARDI VM et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 4; NO 1; PP. 47-50; BIBL. 3 REF.Article

A CHILD WITH PARTIAL TRISOMY 7 AND 20 INHERITED FROM THE MOTHERFELDING I; MITELMAN F.1979; HEREDITAS; SWE; DA. 1979; VOL. 91; NO 1; PP. 91-95Article

HYPO-HYPERPARATHYROIDIE CHEZ UN GARCON PORTEUR D'UNE TRANSLOCATION 8-20 EN MOSAIQUE.FONTAN D; BRENDEL A; SERVILLE F et al.1977; PEDIATRIE; FR.; DA. 1977; VOL. 32; NO 2; PP. 171-179; ABS. ANGL.; BIBL. 27 REF.Article

ATYPICAL CHRONIC MYELOGENOUS LEUKEMIA WITH PHILADELPHIA (PH') CHROMOSOME AND AN ADDITIONAL TRANSLOCATION.NORMAN CS; BOUCHER BJ.1978; CANCER; U.S.A.; DA. 1978; VOL. 41; NO 3; PP. 1123-1127; BIBL. 20 REF.Article

PARTIAL TRISOMY 6P DUE TO FAMILIAL TRANSLOCATION T(6;20) (P21;P23). A NEW SYNDROME.BREUNING MH; BIJLSMA JB; DEFRANCE HF et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 7-13; BIBL. 9 REF.Article

TRISOMY 20PTER -> Q11 IN A MALFORMED BOY FROM A T(13;20)(P11;Q11) TRANSLOCATION-CARRIER MOTHERSCHINZEL A.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 169-172; BIBL. 9 REF.Article