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RING 17 CHROMOSOME DETECTED BY AMNIOCENTESIS = CHROMOSOME 17 ANNULAIRE DECOUVERT PAR AMNIOCENTESEWEINBERG AG; BAIR JL; HARROD MJ et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 3; PP. 269-272; BIBL. 10 REF.Article

CYTOLOGICAL ELUCIDATION OF A 17P MARKER CHROMOSOMESANDSTROM MM; JENKINS EC.1974; CARYOLOGIA; ITAL.; DA. 1974; VOL. 27; NO 3; PP. 307-314; BIBL. 1P.1/2Article

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

INTERPRETATION OF A MARKER CHROMOSOME 17P IN MULTIPLE MYELOMASHABTAI F; HALBRECHT I.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 95; NO 1; PP. 11-14; BIBL. 14 REF.Article

DUPLICATION (PARTIAL TRISOMY) OF THE DISTAL LONG ARM OF CHROMOSOME 17: A NEW CLINICALLY RECOGNIZABLE CHROMOSOME DISORDERBERBERICH MS; CAREY JC; LAWCE HJ et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 287-295; BIBL. 3 REF.Article

ISOCHROMOSOME 17 IN PROSTATIC CANCER = L'ISOCHROMOSOME 17 DANS LE CANCER DE LA PROSTATEOSHIMURA M; SANBERG AA.1975; J. UROL.; U.S.A.; DA. 1975; VOL. 114; NO 2; PP. 249-250; BIBL. 9 REF.Article

TRASLOCAZIONE CROMOSOMICA 6/17 CAUSA DI ABORTI RIPETUTI = TRANSLOCATION CHROMOSOMIQUE 6/17, CAUSE D'AVORTEMENTS REPETESPASQUALI F; MARASCHIO P; ZARA C et al.1973; ANN. OSTETR. GINECOL. MED. PERINAT.; ITAL.; DA. 1973; VOL. 94; NO 9-10; PP. 553-556; ABS. FR. ANGL.; BIBL. 4REF.Article

DUPLICATION (17P) IN A CHILD WITH AN ISODICENTRIC (17P) CHROMOSOMEMASCARELLO JT; JONES MC; HOYME HE et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 67-72; BIBL. 10 REF.Article

TWO CASES OF ACUTE PROMYELOCYTIC LEUKEMIA WITH VARIANT TRANSLOCATIONS: THE IMPORTANCE OF CHROMOSOME NO.17 ABNORMALITY = DEUX CAS DE LEUCEMIE PROMYELOCYTAIRE AIGUE AVEC TRANSLOCATIONS VARIANTES; L'IMPORTANCE DE L'ANOMALIE DU CHROMOSOME NO17YAMADA K; SUGIMOTO E; AMANO M et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 9; NO 2; PP. 93-99; ABS. ENG; BIBL. 19 REF.; FIGArticle

THE ISOCHROMOSOME (179) IN CHRONIC MYELOCYTIC LEUKAEMIA: MECHANISM OF ORIGIN, CENTROMERIC FUNCTION AND CLONAL EVOLUTIONPASQUALI F; PANARELLO C; BERNASCONI P et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 1; PP. 89-90; BIBL. 11 REF.Article

AN INFANT WITH RING 17 CHROMOSOME AND UNUSUAL DERMATOGLYPHS: A NEW SYNDROME .CARPENTER NJ; LEICHTMAN LG; STAMPER S et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 3; PP. 234-236; BIBL. 7 REF.Article

PURE TRISOMY 17P IN 60% OF CELLSSHABTAI F; SHALEV A; CHEMKE J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 3; PP. 263-268; BIBL. 12 REF.Article

FAMILIAL OCCURRENCE OF CHROMOSOME VARIANT 17 PH+.KUBIEN E; KLECZKOWSKA A.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 1; PP. 39-42; BIBL. 14 REF.Article

CHROMOSOME BAND ANALYSIS IN 19 CASES OF CHRONIC MYELOID LEUKEMIA: 9 CHRONIC, 10 BLASTIC, TWO WITH PH1 (22Q-) TRANSLOCATION ON 17 SHORT ARMENGEL E; MCGEE BJ; FLEXNER JM et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 239-240; ABS. FR.; BIBL. 11 REF.Article

17 LONG ARM ISOCHROMOSOME, A COMMON ANOMALY IN MALIGNANT BLOOD DISORDERSENGEL E; MCKEE LC; FLEXNER JM et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 56-60; ABS. FR.; BIBL. 24 REF.Article

A (10; 17) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-216ZACKAL E; MELLMAN W; ARONSON M et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 88-89; BIBL. 1REF.Article

46,XX/47,XY,+17 MOSAICISM IN A NEWBORN WITH SEVERE MALFORMATIONSBULLERDIEK J; BARTNITZKE S.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 3; PP. 296Article

DICENTRIC ISOCHROMOSOME FOR THE LONG ARM OF CHROMOSOME 17, DIC I (17 Q), IN A PATIENT WITH CHRONIC MYELOGENOUS LEUKEMIA (CML)WHANG PENG J; LEE E; KNUTSEN T et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 3; PP. 233-236; BIBL. 18 REF.Article

CYTOCHEMICAL ANALYSIS ON A CASE OF FAMILIAL 17 PSAU W; WITEK JA.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 195-199; BIBL. 19 REF.Article

A (9; 17) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. 6M-988.LIN CC; KAVANAGH AJ; ARONSON MM et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 244Article

ISOCHROMOSOME 17 IN A CASE OF EOSINOPHILIC LEUKAEMIA. AN ABNORMALITY COMMON TO EOSINOPHILIC AND NEUTROPHILIC CELLS = ISOCHROMOSOME 17 AU COURS D'UNE LEUCEMIE A EOSINOPHILES. UNE ANOMALIE COMMUNE AUX CELLULES EOSINOPHILES ET NEUTROPHILEMITELMAN F; PANANI A; BRANDT L et al.1975; SCAND. J. HAEMATOL.; DENN.; DA. 1975; VOL. 14; NO 4; PP. 308-312; BIBL. 21 REF.Article

ISOCHROMOSOME (17Q) IN PHILADELPHIA CHROMOSOME (PH1)-NEGATIVE JUVENILE CHRONIC MYELOCYTIC LEUKEMIACASALONE R; FRANCESCONI D; PASQUALI F et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 2; PP. 145-148; BIBL. 9 REF.Article

TRANSLOCATION T (13;17)(Q14;Q22) FAMILIALE DIAGNOSTIQUEE APRES LA NAISSANCE D'UN ENFANT TRISOMIQUE 21STOLL C; LEVY JM; DORR R et al.1975; J. GENET. HUM.; SUISSE; DA. 1975; VOL. 23; NO 4; PP. 327-334; ABS. ANGL. ALLEM.; BIBL. 2 P. 1/2Article

UNE ABERRATION CHROMOSOMIQUE CHEZ UN MARI COMME CAUSE POSSIBLE DE MALFORMATIONS FOETALESVYLKOVA G; BOJKINOVA E; KATSAROVA M et al.1975; AKUSH. I GINEKOL.; BALG.; DA. 1975; VOL. 14; NO 5; PP. 379-382; ABS. RUSSE ANGL.; BIBL. 28 REF.Article

A G-LIKE TRISOMY WITH A MAJOR 15 PROXIMAL SUPERNUMERARY COMPONENT DERIVED FROM A DIE BALANCED MATERNAL INTERCHANGE = TRISOMIE DE TYPE G AVEC UNE COMPOSANTE 15 PROXIMALE SURNUMERAIRE IMPORTANTE DERIVEE D'UN ECHANGE D/E BALANCE MATERNELBANNISTER DL; ENGEL E.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 86; NO 6; PP. 916-917; BIBL. 5 REF.Article

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