MONOZYGOTIC TWINS WITH RING CHROMOSOME 22 = JUMEAUX MONOZYGOTES PORTEURS D'UN CHROMOSOME 22 ANNULAIRELINDENBAUM RH; BOBROW M; BARBER L et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 85-89; BIBL. 26 REF.Serial Issue

RING F CHROMOSOME MOSAICISM (46,XY,20R/46,XY) IN AN EPILEPTIC CHILD WITHOUT APPARENT HAEMATOLOGICAL DISEASE = MOSAIQUE AVEC CHROMOSOME F ANNULAIRE (46,XY, 20R/46,XY) CHEZ UN ENFANT EPILEPTIQUE SANS MALADIE HEMATOLOGIQUE DEMONTREEFAED M; MORTON HG; ROBERTSON J et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 470-473; BIBL. 14 REF.Serial Issue

ETUDE CYTOGENETIQUE DE LA VARIABILITE DES CHROMOSOMES ANNULAIRES CHEZ DROSOPHILA. I. LEURS EFFETS SUR LE SEXE ET LES DIFFERENTS STADES DU DEVELOPPEMENTSTEPANOVA NL.1972; GENETIKA; S.S.S.R.; DA. 1972; VOL. 8; NO 8; PP. 90-97; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

IL CROMOSOMA 18 AD ANELLO. OSSERVAZIONE CLINICA E CONSIDERAZIONI CARIOLOGICHE = LE CHROMOSOME 18 EN ANNEAU. OBSERVATION CLINIQUE ET ETUDE DU CARYOTYPEGIOVANNUCCI UZIELLI ML; CARBONE C; CALABRI G et al.1972; MINERVA PEDIATR.; ITAL.; DA. 1972; VOL. 24; NO 36; PP. 1707-1714; ABS. ANGL.; BIBL. 31 REF.Serial Issue

D1 RING CHROMOSOME IN NEWBORN WITH PECULIAR FACE, POLYDACTYLY, IMPERFORATE ANUS, ARRHINENCEPHALY, AND OTHER MALFORMATIONS = CHROMOSOME D1 EN ANNEAU CHEZ UN NOUVEAU-NE AVEC FACIES PARTICULIER, POLYDACTYLIE, IMPERFORATION ANALE, ARRHINENCEPHALIE ET D'AUTRES MALFORMATIONSBILES AR JR; LUEERS T; SPERLING K et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 399-401; BIBL. 17 REF.Serial Issue

CHROMOSOME X EN ANNEAUBIEDER J; CHOISEL G; CHOISEL HODICQ D et al.1972; ANN. MEDICO-PSYCHOL.; FR.; DA. 1972; VOL. 130; NO 3; PP. 402-409; BIBL. 1P.1/2Serial Issue

RING D1 CHROMOSOME WITH REMARKABLE MORPHOLOGICAL VARIATION IN A BOY WITH MENTAL RETARDATIONSALAMANCA F; BUENTELLO L; ARMENDARES S et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 3; PP. 183-186; ABS. ANGL.; BIBL. 1 P.Serial Issue

A RING CHROMOSOME (NO18) IN A CYCLOPS = CHROMOSOME NO 18 EN ANNEAU CHEZ UN CYCLOPECOHEN MM; STORM DF; CAPRARO VJ et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 4; PP. 249-252; BIBL. 1P.Serial Issue

A RING-20 CHROMOSOME = UN CHROMOSOME 20 ANNULAIREATKINS L; MILLER WL; SALAM M et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 377-380; BIBL. 4 REF.Serial Issue

RING CHROMOSOME 7 WITH VARIABLE PHENOTYPIC EXPRESSION1973; CYTOGENET. CELL GENET.; SWITZ.; DA. 1973; VOL. 12; NO 1; PP. 40-48; BIBL. 1P.Serial Issue

IDENTIFICATION BY FLUORESCENCE OF TWO G RINGS: (46XY, 21R) G DELETION SYNDROME I AND (46, XX, 22R) G DELETION SYNDROME IIMAGENIS RE; ARMENDARES S; HECHT F et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 265-266; ABS. FR.Serial Issue

CHROMOSOME 15 EN ANNEAU: R (15). IDENTIFICATION PAR DENATURATION MENAGEEFORABOSCO A; DUTRILLAUX B; VAZZOLER G et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 267-270; ABS. ANGL.; BIBL. 14REF.Serial Issue

A CHILD WITH A 21-RING CHROMOSOME, 45,XX,21-/46,XX,21R INVESTIGATED WITH THE BANDING TECHNIQUE = EXPLORATION PAR LA TECHNIQUE DE COLORATION EN BANDES CHEZ UN ENFANT PORTEUR D'UN CHROMOSOME1 ANNULAIRE, 45,XX,21-/46,XX,21^RSHIBATA K; WALDENMAIER C; HIRSCH W et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 4; PP. 315-319; ABS. ALLEM.; BIBL. 15REF.Serial Issue

E₁₈-RINGCHROMOSOM, KASUISTIK UND UEBERSICHT = LE CHROMOSOME E₁₈ EN ANNEAU. CASUISTIQUE ET ETUDE GLOBALEGROSSE KP; SCHWANITZ G; ROTT HD et al.1972; KLIN. PAEDIATR.; DTSCH.; DA. 1972; VOL. 184; NO 6; PP. 495-500; ABS. ANGL.; BIBL. 12REF.Serial Issue

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

PHENOTYPE ASSOCIATED WITH RING 10 CHROMOSOME: REPORT OF PATIENT AND REVIEW OF LITERATUREMICHELS VV; DRISCOLL DJ; LEDBETTER DH et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 231-237; BIBL. 11 REF.Article

HUMAN RING CHROMOSOMES: A REPORT OF FIVE CASESPICCIANO DJ; BERLIN CM; DAVENPORT SLH et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 241-247; ABS. FR.; BIBL. 12REF.Serial Issue

INDUCTION OF GROSS DELETIONS IN RING AND ROD X CHROMOSOMES OF DROSOPHILA1972; TRANS. ILLINOIS STATE ACAD. SCI.; U.S.A.; DA. 1972; VOL. 65; NO 1-2; PP. 3-4; BIBL. 4REF.Serial Issue

SUR UN PHENOMENE D'ENCERCLEMENT DES CHROMOSOMESBORODKIN PA.1978; GENETIKA; SUN; DA. 1978; VOL. 14; NO 12; PP. 2218-2219; ABS. ENG; BIBL. 6 REF.Article

THE EFFECTS OF CHROMOSOME ABNORMALITIES ON BIRTH WEIGHT IN MAN. II. AUTOSOMAL DEFECTS = LES EFFETS DES ANOMALIES CHROMOSOMIQUES SUR LE POIDS DE NAISSANCE CHEZ L'HOMME. II. DEFAUTS AUTOSOMIQUESCHEN ATL; CHAN YK; FALEK A et al.1972; HUM. HERED.; SWITZ.; DA. 1972; VOL. 22; NO 3; PP. 209-224; BIBL. 6P.Serial Issue

TROUBLE PIGMENTAIRE DE LA RETINE EN CAS D'ABERRATION CHROMOSOMIQUEMICHIELS J; STANESCU B; ROMMEL J et al.1972; BULL. MEM. SOC. FR. OPHTALMOL.; FR.; DA. 1972; VOL. 85; PP. 39-130 (11P.); BIBL. 18REF.Serial Issue

RING CHROMOSOME 12 AND LATENT CENTROMERESZUFFARDI O; DANESINO C; POLONI L et al.1980; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1980; VOL. 28; NO 3; PP. 151-157; BIBL. 24 REF.Article

RING CHROMOSOME 13 AND HAPTOGLOBIN HETEROZYGOSITY = CHROMOSOME 13 ANNULAIRE ET HETEROZYGOTIE POUR L'HAPTOGLOBINEFITZGERALD PH.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 1; PP. 25-27; BIBL. 12REF.Serial Issue

THE RING CHROMOSOME 13 SYNDROMEMARTIN NJ; HARVEY PJ; PEARN JH et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 1; PP. 18-23; BIBL. 23 REF.Article

RING CHROMOSOME 14: A DISTINCT CLINICAL ENTITYSCHMIDT R; EVIATAR L; MITOWSKY HM et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 4; PP. 304-307; BIBL. 7 REF.Article