INVERSION PERICENTRIQUE INV (2) (P11 Q13) DANS DES FAMILLES NON APPARENTEESLEONARD C; HAZAEL MASSIEUX P; BOCQUET L et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 2; PP. 121-128; ABS. ANGL.; BIBL. 1P.Article

A (132) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-257ALFI OS; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 154-155Article

Mosaic pericentric inversion of chromosome 2FRYNS, J. P; PETIT, P; HEFFINCK, R et al.Journal de génétique humaine. 1983, Vol 31, Num 2, pp 157-161, issn 0021-7743Article

Interstitial deletion of the long arm of chromosome 2:del(2) (q 31 q 33)AL-AWADI, S. A; FARAG, T. I; NAGUIB, K et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 464-465, issn 0022-2593Article

REPLICATION DU CHROMOSOME 2 DANS 2CARYOTYPES ANORMAUX, CHEZ L'HOMMEPODUGOL'NIKOVA OA.1974; CITOLOGIJA; S.S.S.R.; DA. 1974; VOL. 16; NO 11; PP. 1356-1360; ABS. ANGL.; BIBL. 2REF.Article

TRANSLOCATION 46,XY,T(2;5) (Q37; Q14) ET DEBILITE MENTALE. ETUDE CLINIQUE ET CYTOGENETIQUEGILGENKRANTZ S; WALBAUM R; MAUUARY G et al.1976; J. GENET. HUM.; SUISSE; DA. 1976; VOL. 24; NO 1; PP. 27-37; ABS. ANGL. ALLEM.; BIBL. 6 REF.Article

DELETION 2Q: TWO NEW CASES WITH KARYOTYPES 46,XY,DEL(2)(Q31Q33) AND 46,XX,DEL(2)(Q36)YOUNG RS; SHAPIRO SD; HANSEN KL et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 199-202; BIBL. 6 REF.Article

PARTIAL TRISOMY 2QSCHUMACHER RE; ROCCHINI AP; WILSON GN et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 3; PP. 191-194; BIBL. 9 REF.Article

DIRECT DUPLICATION 2P14->2P23YUNIS E; GONZALEZ J; ZUNIGA R et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 241-244; BIBL. 3 REF.Article

A FRAGILE SECONDARY CONSTRICTION ON CHROMOSOME 2 IN A SEVERELY MENTALLY RETARDED PATIENT.WILLIAMS AJ; HOWELL RT.1977; J. MENTAL DEFIC. RES.; G.B.; DA. 1977; VOL. 21; NO 3; PP. 227-230; BIBL. 11 REF.Article

A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22PARRUTI, G; DI ILIO, C; CALABRESE, G et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 55-58, issn 0003-3995, 4 p.Article

Interstitial deletion of 2 (q33q36) in a child with congenital abnormalitiesGORSKI, J. L; KIYNE, M; UHLMANN, W et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 204-205, issn 0022-2593, 2 p.Article

Interstitial deletion of chromosome 2MARKOVIC, S; KRSTIC, M; SULOVIC, V et al.Journal of medical genetics. 1985, Vol 22, Num 2, pp 154-155, issn 0022-2593Article

A case of deletion 2q35→qter and a peculiar phenotypeSANCHEZ, J. M; PANTANO, A. M.Journal of medical genetics. 1984, Vol 21, Num 2, pp 147-149, issn 0022-2593Article

Response by Dr. WassmanWASSMAN, E. R.American journal of medical genetics. 1988, Vol 29, Num 2, pp 455-456, issn 0148-7299Article

INTERSTITIAL DELETION OF THE SHORT ARM OF CHROMOSOME 2 IN A MODERATELY MENTALLY RETARDED BOY WITHOUT GROSS CLINICAL STIGMATAFRYNS JP; DEWAELE P; VAN DEN BERGHE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 123-125; BIBL. 7 REF.Article

SEGREGATION OF ACP₁ AND MNS_S IN FAMILIES WITH STRUCTURAL REARRANGEMENTS INVOLVING CHROMOSOME 2 = LA SEGREGATION DE ACP₁ ET DE MNS_S DANS DES FAMILLES CONDUCTRICES DE REMANIEMENTS DE STRUCTURE INTERESSANT LE CHROMOSOME 2MACE MA; NOADES J; ROBSON EB et al.1975; ANN. HUM. GENET.; G.B.; DA. 1975; VOL. 38; NO 4; PP. 479-484; BIBL. 18 REF.Article

RING CHROMOSOME 2: CLINICAL, CHROMOSOMAL, AND BIOCHEMICAL ASPECTSJANSEN M; BEEMER FA; VAN DER HEIDEN C et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 1; PP. 91-95; BIBL. 23 REF.Article

PARTIAL DELECTION OF CHROMOSOME 2 MIMICKING A PHENOTYPE OF TRISOMY 18: CASE REPORT WITH AUTROPYMCCONNELL TS; KORNFELD M; MCCLELLAN G et al.1980; HUM. PATHOL.; USA; DA. 1980; VOL. 11; NO 2; PP. 202-205; BIBL. 4 REF.Article

PERICENTRIC INVERSION IN CHROMOSOME NO. 2 AS A DE NOVO MUTATIONHESSELBJERG U; FRIEDRICH U.1979; HUM. GENET.; DEU; DA. 1979; VOL. 53; NO 1; PP. 117-119; BIBL. 10 REF.Article

SUCCESSIVE SPONTANEOUS ABORTIONS INCLUDING ONE WITH WHOLE-ARM TRANSLOCATION BETWEEN CHROMOSOMES 2.OHAMA K; KUSUMI I; TAKAHARA H et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 40; NO 2; PP. 221-225; BIBL. 6 REF.Article

THE CYTOGENETIC AND CLINICAL IMPLICATIONS OF A RING CHROMOSOME 2COTE GB; KATSANTONI A; DELIGEORGIS D et al.1981; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1981; VOL. 24; NO 4; PP. 231-235; ABS. FRE; BIBL. 18 REF.Article

PERICENTRIC INVERSIONS INV (2) (PLL Q 13) AND INV(2)(P13QLL) IN 2 UNRELATED FAMILIES.PHILLIPS RB.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 5; PP. 388-390; BIBL. 7 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

ETUDE CHROMOSOMIQUE ET CLINIQUE D'UNE FILLETTE PORTEUSE D'UNE DELETION (2) (934936)WARTER S; LAUSECKER C; PENNERATH A et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 225-227; BIBL. 3 REF.Article