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

A (1; 15) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-126PRESCOTT GH; MCCAW BK; TOLBY BE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 84-85; BIBL. 1REF.Article

A(Y; 15) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-118HAHNENMANN N; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 408-409Article

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

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

RING CHROMOSOME 15:R(15). IDENTIFICATION BY R BANDING. = CHROMOSOME EN ANNEAU 15:R(15). IDENTIFICATION PAR COLORATION EN BANDES RSTOLL C; JUIF JG; LUCKEL JC et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 259-262; BIBL. 12 REF.Article

Deletion of chromosome 15(q11-13) in a Prader-Labhart-Willi syndrome clinic populationCASSIDY, S. B; THULINE, H. C; HOLM, V. A et al.American journal of medical genetics. 1984, Vol 17, Num 2, pp 485-495, issn 0148-7299Article

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainmentFRACCARO, M; ZUFFARDI, O; GARGANTINI, L et al.Human genetics. 1983, Vol 64, Num 4, pp 388-394, issn 0340-6717Article

De novo partial trisomy 15q (proximal type)HERWEIJER, T. J; OORTHUYS, J. W. E; LESCHOT, N. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, pp 260-262, issn 0022-2593Article

Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three casesWISNIEWSKI, L. P; DOHERTY, R. A.Human genetics. 1985, Vol 69, Num 2, pp 161-163, issn 0340-6717Article

Partial trisomy 15(q25qter) in two brothersKRISTOFFERSSON, U; BERGWALL, B.Hereditas (Landskrona). 1984, Vol 100, Num 1, pp 7-10, issn 0018-0661Article

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

DOWN'S SYNDROME ASSOCIATED WITH TWO ROBERTSONIAN TRANSLOCATIONS, 45,XX,-15, -21, +T(15Q 21Q) AND 46,XX, -21,+T(21Q 21Q)ATKINS L; BARTSOCAS CS.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 306-309; BIBL. 2REF.Article

BANDING IDENTIFICATION OF PARTIAL TRISOMY 15 AND OF 8/21 TRANSLOCATION = IDENTIFICATION PAR COLORATION EN BANDES DE LA TRISOMIE 15 PARTIELLE ET DE LA TRANSLOCATION 8/21WURSTER HILL DH; HOEFNAGEL D.1974; J. MENTAL DEFIC. RES.; G.B.; DA. 1974; VOL. 18; NO 2; PP. 139-144; BIBL. 1P.Article

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

INHERITED T2Q -/15Q + TRANSLOCATION AND DOWN'S SYNDROMESTOLL C; KUSS JJ; SCHNEEGANS E et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 1; PP. 5-7; BIBL. 4 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

KARYOTYP-PHENOTYP-KORRELATION BEI EINEM 46, XDEL (X) (P22)-BEFUND = CORRELATION PHENOTYPE CARYOTYPE DANS UN DIAGNOSTIC 46, XDEL (X) (P22)BARTSCH SANDHOFF M; TERINDE R; WIEGELMANN W et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 3; PP. 263-270; ABS. ANGL.; BIBL. 10 REF.Article

THE 9P-DELETION SYNDROME. REPORT OF A PATIENT WITH A 46,XX,9P-CONSTITUTION DUE TO A PATERNAL T(9P-;15Q+) TRANSLOCATIONORYE E; VERHAAREN H; VAN DEN BOAERT VAN HEESVELDE AM et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 349-357; BIBL. 8 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