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PHILADELPHIA CHROMOSOME WITH T(6;22) (P25;Q12)MAMMON Z; GRINBLAT J; JOSHUA H et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 16; PP. 827-828; BIBL. 8 REF.Article

A (17; 22) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-119MACINTYRE MN; HEMPEL JM; WALDEN DB et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 80-81; BIBL. 2REF.Article

FAMILIAL 21/22 TRANSLOCATIONPAPP Z; DOLHAY B; GARDO S et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 69-73; ABS. ITAL. FR. ALLEM.; BIBL. 18 REF.Article

SEGREGATION OF A T(14Q22Q) CHROMOSOME IN A LARGE KINDRED = SEGREGATION D'UN CHROMOSOME T(14Q22Q) DANS UNE GRANDE FAMILLENEU RL; VALENTINE FA; GARDNER LI et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 1; PP. 30-36; BIBL. 14 REF.Article

LA SINDROME R(22). = LE SYNDROME R(22)CURATOLO P; PAOLELLA A; PORRO G et al.1978; CLIN. PEDIATR.; ITAL.; DA. 1978; VOL. 60; NO 1; PP. 10-17; ABS. ANGL.; BIBL. 11 REF.Article

UNEXPECTED FINDINGS WITH THE NEW CHROMOSOME BANDING TECHNIQUES IN A PATIENT FORMERLY DIAGNOSED AS HAVING G-DELETION SYNDROME = RESULTATS INATTENDUS OBTENUS GRACE AUX NOUVELLES TECHNIQUES DE BANDES CHEZ UNE PATIENTE DIAGNOSTIQUEE INITIALEMENT COMME ATTEINTE DE SYNDROME II DE DELETION GORYE E; CRAEN M.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 75-82; ABS. ITAL. FR. ALLEM.; BIBL. 14 REF.Article

ETUDE D'UN SUJET AVEC CARYOTYPE 46, XY, 22 P+.TRABALZA N; FURBETTA M; ROSI G et al.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 2; PP. 177-184; ABS. ENG/GER; BIBL. 24 REF.Article

A CASE OF PARTIAL TRISOMY 22 WITHOUT CAT-EYE STIGMATAKADOTANI T; KATANO T; YAMAOKA H et al.1978; PROC. JAP. ACAD. B; JPN; DA. 1978; VOL. 54; NO 5; PP. 217-221; BIBL. 9 REF.Article

A NEW TRANSLOCATION IN CHRONIC MYELOGENOUS LEUKEMIAPRAVTCHEVA D; ANDREEVA P; TSANEVA R et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 229-232; BIBL. 11 REF.Article

TRANSMISSION OF A T(13Q22Q) CHROMOSOME ABSERVED IN THREE GENERATIONS WITH SEGREGATION OF THE TRANSLOCATION D1-TRISOMY SYNDROMEABE T; MORITA M; KAWAI K et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 207-215; BIBL. 21 REF.Article

DEUX CAS DE TRISOMIE 11Q (Q231-QTER) PAR TRANSLOCATION T(11,22) (Q231; Q111) DANS DEUX FAMILLES DIFFERENTES.AURIAS A; TURC C; MICHIELS Y et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 185-188; ABS. ANGL.; BIBL. 9 REF.Article

TRISOMIE 9P PAR TRANSLOCATION MATERNELLE (9;22)(P11;Q11)PHILIPPE N; REQUIN C; GERMAIN D et al.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 4; PP. 309-317; ABS. ANGL. ALLEM.; BIBL. 1 P. 1/2Article

DUPLICATION OF THE SEGMENT Q122->QTER OF CHROMOSOME 22 DUE TO PATERNAL INVERSION 22 (P13Q122)FUJIMOTO A; WILSON MG; TOWNER JW et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 82-84; BIBL. 3 REF.Article

PHENOTYPIC VARIATION IN TWO PATIENTS WITH A RING CHROMOSOME 22FUNDERBURK SJ; SPARKES RS; KLISAK I et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 5; PP. 305-310; BIBL. 23 REF.Article

TRISOMIA 4P DA TRASLOCAZIONE T (4 P-, 22P+). INDAGINE FAMILIARE SU QUATTRO GENERAZIONI = TRISOMIE 4P PAR TRANSLOCATION T (4P-, 22P+). ETUDE FAMILIALE SUR 4 GENERATIONSFORABOSCO A; GIOVANNELI G; MARZONA L et al.1976; MINERVA PEDIATR.; ITAL.; DA. 1976; VOL. 28; NO 12; PP. 743-751; ABS. ANGL.; BIBL. 6 REF.Article

A 9/11 TRANSLOCATION IN A CHILD WITH PH1-NEGATIVE CHRONIC MYELOGENOUS LEUKEMIA = TRANSLOCATION 9/11 CHEZ UN ENFANT ATTEINT D'UNE LEUCEMIE MYELOGENE CHRONIQUE PH1-NEGATIVEWARBURTON D; NARAYAN SHAH.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 8; NO 4 PART. 1; PP. 599-601; BIBL. 10 REF.Article

BALANCED HOMOLOGOUS TRANSLOCATION T (22Q 22Q) IN A PHENOTYPICALLY NORMAL WOMAN WITH REPEATED SPONTANEOUS ABORTIONS. = TRANSLOCATION HOMOLOGUE BALANCEE T (22Q 22Q) CHEZ UNE FEMME PHENOTYPIQUEMENT NORMALE AVEC AVORTEMENTS SPONTANES REPETESFARAH LMS; NAZARETH HR DE S; DOLNIKOFF M et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 357-360; BIBL. 14 REF.Article

THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22KELLEY RI; ZACKAI EH; EMANUEL BS et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 2; PP. 197-200; BIBL. 22 REF.Article

CHROMOSOME 22 EN ANNEAU: R(22)TEYSSIER M; MOREAU N.1982; BULL. ASSOC. ANAT.; ISSN 0376-6160; FRA; DA. 1982; VOL. 66; NO 193; PP. 273-282; ABS. ENG; BIBL. 2 P.Article

TRISOMY 22 SYNDROME IN A 26-YEAR-OLD FEMALE: A FOLLOW-UP EXAMINATIONANNEREN G; GUSTAVSON KH.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 94; NO 1; PP. 67-71; BIBL. 10 REF.Article

TRISOMIE 22 PARTIELLE.TAILLEMITE JL; BAHEUX MORLIER G; VAN DEN AKKER J et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 291-293; ABS. ANGL.; BIBL. 15 REF.Article

TRISOMY OF THE SHORT ARM OF CHROMOSOME 10NAKAGOME Y; KOBAYASHI H.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 412-414; BIBL. 4 REF.Article

TRISOMIE POUR LES BRAS COURTS DU CHROMOSOME 9 (SYNDROME +9P). A PROPOS D'UNE OBSERVATION PAR TRANSLOCATION MATERNELLE 9-22GERMAIN D; PHILIPPE N; HERMIER M et al.1975; LYON MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 227-230; ABS. ANGL.; BIBL. 19REF.Article

A FAMILIAL X-22 TRANSLOCATION WITH AN EXTRA X CHROMOSOME = UNE TRANSLOCATION FAMILIALE X-22 AVEC UN EXTRA-CHROMOSOME XJENKINS MB; DAVIS E; THELEN TH et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 26; NO 6; PP. 736-745; BIBL. 18REF.Article

TWO SUCCESSIVE PARTIAL TRISOMIES FOR OPPOSITE HALVES OF CHROMOSOME 22 IN A MOTHER WITH A BALANCED TRANSLOCATIONBENDEL RP; BALDINGER S; MILLARD C et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 313; BIBL. 2 REF.Article

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