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AN (X; 3) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-194DE LA CHAPELLE A; SCHROEDER J; KLINGER HP et al.1975; CYTOGENET. CELL. GENET.; SWITZ.; DA. 1975; VOL. 15; NO 6; PP. 404-405; BIBL. 1 REF.Article

A SECOND PATIENT WITH PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 3: KARYOTYPE 46,XY,DEL(3) (P25)HIGGINBOTTOM MC; MASCARELLO JT; HASSIN H et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 1; PP. 71-73; BIBL. 2 REF.Article

DUPLICATION 3 P SYNDROME: REPORT OF A NEW CASE AND REVIEW OF THE LITERATURECHARROW J; COHEN MM; MEEKER D et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 4; PP. 431-436; BIBL. 16 REF.Article

DUPLICATION 3Q: SEVERE MANIFESTATIONS IN AN INFANT WITH DUPLICATION OF A SHORT SEGMENT OF 3QROSENFELD W; VERMA RS; JHAVERI RC et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 2; PP. 187-192; BIBL. 27 REF.Article

A CASE OF PARTIAL 3P TRISOMY (46,XY,-18,+DER(18),T(3; 18) (P24; Q22))TSUKINO R; OMORI H; UEMURA S et al.1981; PROC. JPN. ACAD., SER. B; ISSN 0386-2208; JPN; DA. 1981; VOL. 57; NO 3; PP. 89-94; BIBL. 8 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 3MARTSOLF JT; RAY M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 2; PP. 98-99; ABS. FRE; BIBL. 4 REF.Article

PH1-POSITIVE CML ASSOCIATED WITH MEGAKARYOCYTIC HYPERPLASIA AND THROMBOCYTHEMIA AND AN ABNORMALITY OF CHROMOSOME NO 3CARBONELL F; HOELZER D; THIEL E et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 6; NO 2; PP. 153-161; BIBL. 19 REF.Article

THE 4P-SYNDROME: AN AUTOPSY STUDYFERNANDES BJ; GARDNER HA; BEDARD YC et al.1980; HUM. PATHOL.; ISSN 0046-8177; USA; DA. 1980; VOL. 11; NO 6; PP. 683-685; BIBL. 33 REF.Article

A NEW TRANSLOCATION IN CHRONIC MYELOGENOUS LEUKEMIAPRAVTCHEVA D; ANDREEVA P; TSANEVA R et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 229-232; BIBL. 11 REF.Article

INVERSION PERICENTRIQUE DU 3, HOMOZYGOTE ET HETEROZYGOTE, ET TRANSLATION CENTROMERIQUE DU 12 DANS UNE FAMILLE D'ORANGS-OUTANGS. IMPLICATIONS EVOLUTIVESTURLEAU C; DE GROUCHY J; CHAVIN COLIN F et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 4; PP. 227-233; ABS. ANGL.; BIBL. 14 REF.Article

A FAMILIAL PARACENTRIC INVERSION IN THE SHORT ARM OF CHROMOSOME 3: A CASE REPORTPETERS SLOUGH MF; PLANTEYDT HT; TIMMERMAN MJ et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 2; PP. 102-104; BIBL. 8 REF.Article

A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN THREE CHROMOSOMES = TRANSLOCATION RECIPROQUE FAMILIALE ENTRE TROIS CHROMOSOMESCREASY MR; CROLLA JA; DAKER MG et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 4; PP. 303-308; BIBL. 10REF.Article

Familial paracentric inversion inv(3)(q21q25.1): case report and review of the literatureDJALALI, M; STEINBACH, P; BARBI, G et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 41-44, issn 0003-3995Article

Sperm chromosome analysis of a man heterozygous for a pericentric inversion of chromosome 3BALKAN, W; BURNS, K; MARTIN, R. H et al.Cytogenetics and cell genetics. 1983, Vol 35, Num 4, pp 295-297, issn 0301-0171Article

DE NOVO del(3)(q2800)ALVAREZ ARRATIA, M. C; RIVERA, H; MOLLER, M et al.Annales de génétique (Paris). 1984, Vol 27, Num 2, pp 109-111, issn 0003-3995Article

DIFFERENT PATTERNS OF X CHROMOSOME INACTIVITY IN LYMPHOCYTES AND FIBROBLASTS OF A HUMAN BALANCED X; AUTOSOME TRANSLOCATIONHELLKUHL B; DE LA CHAPELLE A; GRZESCHIK KH et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 126-129; BIBL. 20 REF.Article

PARTIAL TRISOMY 3Q DUE TO A DE NOVO TRANSLOCATION T(X;3) (P21;Q12)OORTHUYS JWE; SLATER RM; BARROUGLOUGH H et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 20; NO 2; PP. 130-134; BIBL. 18 REF.Article

DELETION PARTIELLE DU BRAS COURT DU CHROMOSOME 3. A PROPOS D'UN CASGONZALES J; LESOURD S; BRACONNIER A et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 119-122; ABS. ENG; BIBL. 20 REF.Article

FAMILIAL PARTIAL TRISOMY 10Q (Q23->QTER) SYNDROME AND PARACENTRIC INVERSION 3(Q13 Q26) IN THE SAME PATIENTBASS HN; SPARKES RS; CRANDALL BF et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 74-77; ABS. FRE; BIBL. 18 REF.Article

RING CHROMOSOME 3 IN A RETARDED BOY.WITKOWSKI R; ULLRICH E; PIEDE U et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 345-348; BIBL. 8 REF.Article

TRISOMY 11Q (Q21->QTER)BADER PI; JANSCH M; HOFFMAN D et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 383-392; BIBL. 14 REF.Article

VARIANT CHROMOSOME 3 (INV3) IN NORMAL NEWBORNS AND THEIR PARENTS, AND IN CHILDREN WITH MENTAL RETARDATION.MIKELSAAR AV; ILUS T; KIVI S et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 1; PP. 109-113; BIBL. 5 REF.Article

PARTIAL TRISOMI 3Q IN A NEWBORN FEMALE.DE MARCHI M; ZUFFARDI O; CAROZZI F et al.1977; RIC. CLIN. LAB.; ITAL.; DA. 1977; VOL. 7; NO 3; PP. 225-232; BIBL. 10 REF.Article

, XY, T(3; 22) (P2; Q13) RESULTING IN PARTIAL TRISOMY FOR THE SHORT ARM OF CHROMOSOME 3.SURANA RB; BRAUDO ME; CONEN PE et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 201-206; BIBL. 15 REF.Article

UNEINHEITLICHER PHAENOTYP BEI PARTIALTRISOMIE 4Q = VARIATION PHENOTYPIQUE DANS LA TRISOMIE 4Q PARTIELLEVOGEL W; SIEBERS JW; GUNKEL J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 2; PP. 103-112; ABS. ALLEM.; BIBL. 19REF.Article

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