9;22;15 COMPLEX TRANSLOCATION IN PH¹ CHROMOSOME POSITIVE CML REVEALED BY GIEMSA-11 PROCEDURE IN APPARENT LYMPHOID CELLS OF BLASTIC CRISISHAYS T; MORSE HG; ROBINSON A et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 4; PP. 283-292; BIBL. 16 REF.Article

FAMILIAL Y-AUTOSOME TRANSLOCATION IN TWO UNRELATED GIRLSFUNDERBURK SJ; KLISAK I; SPARKES RS et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 119-122; ABS. FRE; BIBL. 24 REF.Article

UNSTABLE FAMILIAL TRANSLOCATIONS: A T(11;22) MAT INHERITED AS A T(11;15)TOMKINS DJ.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 5; PP. 745-751; BIBL. 24 REF.Article

Partial monosomy 15q due to de novo t(15; 22)(q15;p11)MORI, M. A; RODRIGUEZ, L; PINEL, I et al.Annales de génétique (Paris). 1987, Vol 30, Num 4, pp 246-248, issn 0003-3995Article

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

A (14; 15) ROBERTSONIAN TRANSLOCATION, 45 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-479.GOLBUS MS; EPSTEIN CJ; ARONSON MM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 1; PP. 61Article

Y/AUTOSOMAL TRANSLOCATIONS.NIELSEN J; RASMUSSEN K.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 6; PP. 609-617; BIBL. 22 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 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

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 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

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

A DICENTRIC NO. 15 CHROMOSOME WITH TWO SATELLITE REGIONS.WATSON EJ; SCRIMGEOUR JB.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 5; PP. 381-383; BIBL. 7 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

CYTOGENETIC POLYMORPHISM OR Y/15 TRANSLOCATION IN A BLACK MALE WITH AMBIGOUS GENITALIAVERMA RS; DOSIK H; JHAVERI RC et al.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 4; PP. 405-409; ABS. ENG/GER; BIBL. 13 REF.Article

POLYMORPHIC VARIANTS IN HUMAN CHROMOSOME 15CHEN TR; KAO ML; MARKS J et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 1; PP. 61-66; BIBL. 45 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

LATERAL ASYMMETRY IN HUMAN CHROMOSOMES 1, 3, 4, 15, AND 16BRITO BABAPULLE V.1981; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1981; VOL. 29; NO 4; PP. 198-202; BIBL. 16 REF.Article

LATERAL ASYMMETRY IN HUMAN CONSTITUTIVE HETEROCHROMATIN: FREQUENCY AND INHERITANCE.ANGELL RR; JACOBS PA.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 144-152; BIBL. 9 REF.Article

A FAMILIAL TANDEM TRANSLOCATION (15; 21) (Q11; Q22) IN A CASE OF DOWN'S SYNDROME.WAHLSTROEM J; DJERF S.1976; J. MENTAL DEFIC. RES.; G.B.; DA. 1976; VOL. 20; NO 3; PP. 171-178; BIBL. 12 REF.Article

INHERITED PARTIAL TRISOMY 8Q (22->QTER).TOWNES PL; WHITE MR.1978; AMER. J. DIS. CHILD.; U.S.A.; DA. 1978; VOL. 132; NO 5; PP. 498-501; BIBL. 20 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

SYNDROME +12P. CASE REPORT AND REVIEW.TENCONI R; PIOVAN E; PRETO A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 1; PP. 97-101; BIBL. 10 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

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