TRISOMIE 15 PARTIELLE PROXIMALE. ASPECTS CYTOGENETIQUES ET CLINIQUES. ETUDE DE 2 NOUVELLES OBSERVATIONSMISSON FRANCK.1980; ; FRA; THIERS: IMPR. LE POINT; DA. 1980; 17; 165 P.-3 PL.: ILL.; 30 CM; H.T. 2; BIBL. 75 REF.; TH.: MED./CLERMONT 1/1980Thesis

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 15FRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 59-60; ABS. ENG; BIBL. 4 REF.Article

MOSAICISME CHROMOSOMIQUE DANS LE SYNDROME DU 15 EN ANNEAUMALYGINA NA; MUTOVIN GR; FILINA NP et al.1980; GENETIKA; ISSN 0016-6758; SUN; DA. 1980; VOL. 16; NO 11; PP. 2029-2033; H.T. 2; ABS. ENG; BIBL. 12 REF.Article

CONTRIBUTO ALLA PATOLOGIA DEL CROMOSOMA 22. = CONTRIBUTION A LA PATHOLOGIE DU CHROMOSOME 22GIORDANO A; GRIMOLDI MG; LAVEZZI AM et al.1976; FOLIA HERED. PATHOL.; ITAL.; DA. 1976; VOL. 25; NO 2; PP. 38-52; ABS. ANGL.; BIBL. 1 P. 1/2Article

TRISOMIE 15 PARTIELLE: 47, XY, +DEL(15) (Q21)ECHENNE B; EMBERGER JM; FLORENSA G et al.1981; PEDIATRIE; ISSN 0031-4021; FRA; DA. 1981; VOL. 36; NO 7; PP. 551-555; ABS. ENG; BIBL. 22 REF.Article

A NEW CASE OF PRADER-WILLI SYNDROME WITH CHROMOSOMAL ABERRATIONMORIC PETROVIC S; LACA Z; KRSTIC A et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 6; PP. 481; BIBL. 2 REF.Article

PARTIAL TRISOMY OF CHROMOSOME 15.HOWARD PEEBLES PN; YARBROUGH K; STODDARD GR et al.1977; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1977; VOL. 81; NO 6; PP. 606-609; BIBL. 15 REF.Article

TRANSLOCATION D/D INVOLING TWO HOMOLOGOUS CHROMOSOMES OF THE PAIR 15.ZIZKA J; BALICEK P; FINKOVA A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 1; PP. 123-125; BIBL. 4 REF.Article

TWO CHILDREN WITH A PARTIAL TRISOMY OF CHROMOSOME 15 (47, XX, +15).PARKER CE; JAMSHED MAVALWALA; ALFI OS et al.1977; CLIN. PEDIATR.; U.S.A.; DA. 1977; VOL. 16; NO 11; PP. 1037-1041; BIBL. 25 REF.Article

RING CHROMOSOME 15 IN CHILD WITH A MINOR DYSMORPHISM OF PHENOTYPE.RUMENIE L; JOKSIMOVIC I; ANAF M et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 187-188; BIBL. 5 REF.Article

ANALYSIS OF BANDING PATTERNS AND MOSAIC CONFIGURATIONS IN A CASE OF RING CHROMOSOME 15.SCHMID M; HENRICHS I; NESTLER H et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 289-299; BIBL. 30 REF.Article

RING CHROMOSOME 15 SYNDROMEFRYNS JP; TIMMERMANS J; D'HONDT F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 43-48; BIBL. 9 REF.Article

ULTRASTRUCTURAL AND CHROMOSOMAL STUDIES IN A PATIENT WITH HYPERGRANULAR (M₃) PROMYELOCYTIC LEUKEMIA WITH TWO ABNORMAL CLONESZAHAVI I; SHABTAI F; APPEL S et al.1982; ACTA HAEMATOLOGICA; ISSN 0001-5792; CHE; DA. 1982; VOL. 68; NO 1; PP. 52-57; BIBL. 17 REF.Article

RING (15) CHROMOSOMEYUNIS E; LEIBOVICI M; QUINTERO L et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 207-209; BIBL. 14 REF.Article

NUCLEOLUS ORGANIZER AND SATELLITE ASSOCIATION IN A VARIANT D-GROUP CHROMOSOME.DE CAPOA A; FERRARO M; ARCHIDIACONO N et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 1; PP. 13-16; BIBL. 24 REF.Article

THE CHILD WITH CHROMOSOME RING 15WISNIEWSKI L; PRONICKA E; LECH H et al.1979; KLIN. PAEDIATR.; DEU; DA. 1979; VOL. 191; NO 4; PP. 429-432; ABS. GER; BIBL. 13 REF.Article

PREFERENTIAL DERIVATION OF ABNORMAL HUMAN G-GROUP-LIKE CHROMOSOMES FROM CHROMOSOME 15.SCHRECK RR; BREG WR; ERLANGER BF et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 1; PP. 1-12; BIBL. 20 REF.Article

De novo interstitial direct duplication of 15q:46, XY, dir dup (15) (pter→q24::q14→q21.1::q24→qter)HERR, H. M; SCOTT, C. I. JR; HORTON, S. J et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 473-475, issn 0022-2593Article

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

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 casesMATTEI, J. F; MATTEI, M. G; GIRAUD, F et al.Human genetics. 1983, Vol 64, Num 4, pp 356-362, issn 0340-6717Article

TWO FAMILIAL CASES OF TRISOMY 15Q DIST DUE TO A RCP (5; 15) (P14; Q21)TZANCHEVA M; KRACHOUNOVA M; DAMJANOVA Z et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 275-277; BIBL. 5 REF.Article

PARTIAL TRISOMY 15 AND INTRACTABLE SEIZURESTAYSI K; DEVIVO DC; SEKHON GS et al.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 3; PP. 445-447Article

TWO CASES OF PARTIAL TRISOMY 10Q IN THE SAME FAMILY CAUSED BY PARENTAL DIRECT INSERTION (INS. (15; 10) (Q15; Q24Q26))BACK E; KOSMUTZKY J; SCHUWALD A et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 195-198; ABS. FRE; BIBL. 19 REF.Article

PARTIAL TRISOMY 15 AND TEMPORAL LOBE SYNDROME IN A RETARDED GIRL WITHOUT GROSS MALFORMATIONSHONGELL K; IIVANAINEN M.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 4; PP. 229-234; BIBL. 6 REF.Article

LA SINDROME R(15) (CROMOSOMA 15 AD ANELLO). DESCRIZIONE DI UN CASO. = LE SYNDROME R(15) (CHROMOSOME 15 EN ANNEAU). DESCRIPTION D'UN CASFERRANTE E; BOSCHERINI B; BRUNI L et al.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 36; PP. 2163-2168; ABS. ANGL.; BIBL. 6 REF.Article