Anomalies of the long arm of chromosome 11 in human myelo- and lymphoproliferative disorders. I: Acute nonlymphocytic leukemia = Anomalies du bras long du chromosome 11 dans les affections myélo- et lymphoprolifératives. I. Leucémie aiguë non lymphoïdeVERMAELEN, K; BARBIERI, D; MICHAUX, J.-L et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 105-116, issn 0165-4608Article

The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesISELIUS, L; LINDSTEN, J; DUTRILLAUX, B et al.Human genetics. 1983, Vol 64, Num 4, pp 343-355, issn 0340-6717Article

CHROMOSOME II LONG ARM PARTIAL DELETION: A NEW SYNDROMEENGEL E; HIRSHBERG CS; CASSIDY SB et al.1976; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1976; VOL. 80; NO 4; PP. 473-475; BIBL. 3 REF.Article

DEUX OBSERVATIONS DE TRISOMIE 11Q(Q23.I->QTER) AVEC LA MEME ANOMALIE DES ORGANES GENITAUX EXTERNES.LAURENT C; BIEMONT MC; BETHENOD M et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 179-184; ABS. ANGL.; BIBL. 4 REF.Article

A (4;11) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-380KOUSSEFF BG; KIM HJ; HSU LYF et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 150-151Article

A CASE WITH 46,XX,DEL(11)(Q21) = UN CAS DE 46,XX,DEL(11)(Q21)FAUST J; VOGEL W; LONING B et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 90-97; BIBL. 1P.1/2Article

Partial deletion of the long arm of chromosome 11: prenatal diagnosisCHUDLEY, A. E; PABELLO, P. D; PINNO, E et al.American journal of medical genetics. 1983, Vol 16, Num 1, pp 137-139, issn 0148-7299Article

FAMILIAL MENTAL RETARDATION IN A FAMILY WITH AN INHERITED CHROMOSOME REARRANGEMENT = ARRIERATION MENTALE FAMILIALE DANS UNE FAMILLE CONDUCTRICE D'UN REMANIEMENT CHROMOSOMIQUE HEREDITAIRECHUDLEY AE; BAUDER F; RAY M et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 4; PP. 353-366; BIBL. 40REF.Article

DEUX NOUVEAUX CAS DE MONOSOMIE 11Q PARTIELLE AVEC POINT DE CASSURE EN 11Q24LAURENT C; BIEMONT MC; VEYRON M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 239-241; ABS. ENG; BIBL. 13 REF.Article

DE NOVO (11; 13) TRANSLOCATIONFONATSCH C; FLATZ SD; STENDEL A et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 2; PP. 87-91; BIBL. 10REF.Article

47, XY, T(9P+; 11Q+) IN A MALE INFANT WITH MULTIPLE MALFORMATIONS = , XY, T (9P+; 11Q+) CHEZ UN NOURRISSON MALE POLYMALFORMEDINNO ND; SILVEY GL; WEISSKOPF B et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 125-131; BIBL. 11REF.Article

ANOMALIES ASSOCIATED WITH PARTIAL DELETION OF LONG ARM OF CHROMOSOME 11 = ANOMALIES ASSOCIEES A UNE DELETION PARTIELLE DU BRAS LONG DU CHROMOSOME 11LINARELLI LG; GOPALKRISHNAPAI K; PAN SF et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 86; NO 5; PP. 750-752; BIBL. 2 REF.Article

TRANSLOCATION T (11; 20) ET POLYGLOBULIE PRIMITIVE.BERGER R.1975; NOUV. PRESSE MED.; FR.; DA. 1975; VOL. 4; NO 27; PP. 1972; BIBL. 4 REF.Article

Chromosomes in myelodysplastic syndrome: structural abnormalities of chromosome 11MUSILOVA, J; MICHALOVA, K; JAROSOVA, M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 43-46, issn 0003-3995, 4 p.Article

Translocation t(11;14) and trisomy 11q13→qter in multiple myelomaVENTI, G; MECUCCI, C; DONTI, E et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 53-55, issn 0003-3995Article

Interstitial deletion of 11qGUC-SCEKIC, M; PILIC-RADIVOJEVIC, G; MRDJENOVIC, G et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 205-206, issn 0022-2593, 2 p.Article

Deficiency of all or part of chromosome 11 in several types of cancer: significance of a reduction in the number of normal chromosomes 11ATKIN, N. B; BAKER, M. C.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 106-107, issn 0301-0171Article

ISOLATED PERIPHERAL THROMBOCYTOPENIA AS PRESENTING SYMPTOM IN PRELEUKEMIA: A REPORT OF TWO CASES WITH 11Q+TRICOT G; VAN DEN BERGHE H.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 5; NO 2; PP. 147-151; BIBL. 8 REF.Article

PARTIAL MONOSOMY OF THE LONG ARM OF CHROMOSOME 11 IN A SEVERELY AFFECTED CHILDLEE ML; SCIORRA LJ.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 51-53; ABS. FRE; BIBL. 4 REF.Article

DUPLICATION U(0,21 TO 23->QTER) SYNDROME.FRANCKE U; WEBER F; SPARKES RS et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 167-186; BIBL. 12 REF.Article

TRISOMY 4P IN A FAMILY WITH A T (4;15)HUSTINX TWJ; GABREELS FJM; KIRKELS VGHJ et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 13-19; ABS. FR.; BIBL. 25REF.Article

FAMILIAL PERICENTRIC INVERSION OF CHROMOSOME 11 DETECTED PRENATALLYRUSSEL MH; MILLER R; KILLAM A et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 151-152; BIBL. 8 REF.Article

ABSENCE OF CONSTITUTIVE HETEROCHROMATIN IN A PARTIALLY IDENTIFIED SUPERNUMERARY MARKER CHROMOSOMEPAL GS; THOMAS GH; BENKE P et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 392-394; BIBL. 7 REF.Article

DELETION INTERSTITIELLE DU BRAS LONG D'UN CHROMOSOME 11TAILLEMITE JL; BAHEUX MORLIER G; ROUX C et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 61-63; ABS. ANGL.; BIBL. 3 REF.Article

TRISOMIE PARTIELLE 119 ET TRANSLOCATION FAMILIALE 11-22.GIRAUD F; MATTEI JF; MATTEI MG et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 343-347; ABS. ANGL.; BIBL. 9 REF.Article