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kw.\*:("ABNORMAL E17 CHROMOSOME")

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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

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

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

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 (15;17) in a child with variant form of acute promyelocytic leukemia = Translocation (15; 17) chez un enfant présentant une variante de leucémie aiguë promyélocytairePRIETO, F; BADIA, L; CASTEL, V et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 117-120, issn 0165-4608Article

15; 17 TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKEMIAFERRO MT; SAN ROMAN C; FERNANDEZ RANADA JM et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 1; PP. 89-92; BIBL. 3 REF.Article

FAMILIAL TRANSLOCATION T(1;17)STEINBACH P.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 444Article

A CASE OF PARTIAL TRISOMY 17 RESULTING FROM X-AUTOSOMAL TRANSLOCATIONYAMAMOTO Y; ENDO Y; KUROKI Y et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 5; PP. 395-399; BIBL. 6 REF.Article

CHROMOSOME ABERRATION IN ECTOPIA CORDIS (46, XX, 17Q+).SAY B; WILSEY CE.1978; AMER. HEART J.; U.S.A.; DA. 1978; VOL. 95; NO 2; PP. 274-275; BIBL. 1 REF.Article

FURTHES EVIDENCE FOR A NON-RANDOM CHROMOSOMAL ABNORMALITY IN ACUTE PROMYELOCYTIC LEUKEMIA.ROWLEY JD; GOLOMB HM; VARDIMAN J et al.1977; INTERNATION. J. CANCER; SWITZ.; DA. 1977; VOL. 20; NO 6; PP. 869-872; ABS. FR.; BIBL. 13 REF.Article

LA TRISOMIE 17PRETHORE MO; RENAULT F; LAFOURCADE J et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 17-20; ABS. ENG; BIBL. 8 REF.Article

PARTIAL DUPLICATION OF 177P. A NEW CHROMOSOMAL SYNDROMEBARTSCH SANDHOFF M; HIERONIMI G.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 123-127; BIBL. 5 REF.Article

PARTIAL TRISOMY 17Q. KARYOTYPE: 46, XY, DER (21), T(17; 21) (Q22; P13)FRYNS JP; PARLOIR C; VAN DEN BERGHE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 3; PP. 361-364; BIBL. 6 REF.Article

15/17 CHROMOSOME TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKEMIASHEER D; SOLOMON E; GREAVES MF et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 5; NO 4; PP. 353-354; BIBL. 5 REF.Article

BRIEF CLINICAL REPORT: THE DUP(17P) SYNDROMEFELDMAN GM; BAUMER JG; SPARKES RS et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 3; PP. 299-304; BIBL. 7 REF.Article

PARTIAL MONOSOMY AND PARTIAL TRISOMY FOR DIFFERENT SEGMENTS OF CHROMOSOME 13 IN SEVERAL INDIVIDUALS OF THE SAME FAMILY.WILROY RS; SUMMITT RL; MARTENS P et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 237-242; ABS. FR.; BIBL. 6 REF.Article

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